DD248274A5 - Mikrobizides mittel - Google Patents

Mikrobizides mittel Download PDF

Info

Publication number: DD248274A5
Authority: DD; German Democratic Republic
Prior art keywords: formula; plants; triazol; chlorophenoxy; active ingredient
Prior art date: 1983-05-19

Application number

DD84281418A

Other languages

German (de)

English (en)

Inventor

Robert Nyfeler

Original Assignee

��`��@��k��

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1983-05-19

Filing date

1984-05-17

Publication date

1987-08-05

1984-05-17 Application filed by ��`��@��k�� filed Critical ��`��@��k��

1987-08-05 Publication of DD248274A5 publication Critical patent/DD248274A5/de

Links

230000003641 microbiacidal effect Effects 0.000 title claims description 8
239000002855 microbicide agent Substances 0.000 title claims description 4
229940124561 microbicide Drugs 0.000 title 1
150000001875 compounds Chemical class 0.000 claims abstract description 28
239000004480 active ingredient Substances 0.000 claims description 28
239000000203 mixture Substances 0.000 claims description 24
-1 4-chlorophenoxy Chemical group 0.000 claims description 13
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
239000007787 solid Substances 0.000 claims description 7
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 6
125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
239000004094 surface-active agent Substances 0.000 claims description 6
239000000654 additive Substances 0.000 claims description 5
239000007788 liquid Substances 0.000 claims description 4
125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 3
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 3
125000005394 methallyl group Chemical group 0.000 claims description 3
239000001273 butane Substances 0.000 claims 2
125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims 1
ATUOYWHBWRKTHZ-UHFFFAOYSA-N dimethylmethane Natural products CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 claims 1
239000001294 propane Substances 0.000 claims 1
LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 abstract description 11
239000002253 acid Substances 0.000 abstract description 9
239000003795 chemical substances by application Substances 0.000 abstract description 9
238000002360 preparation method Methods 0.000 abstract description 8
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 abstract description 6
238000000034 method Methods 0.000 abstract description 5
150000003852 triazoles Chemical class 0.000 abstract description 5
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract description 4
229910052739 hydrogen Inorganic materials 0.000 abstract description 4
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 abstract description 4
150000002148 esters Chemical class 0.000 abstract description 3
239000003377 acid catalyst Substances 0.000 abstract description 2
239000011230 binding agent Substances 0.000 abstract description 2
239000001257 hydrogen Substances 0.000 abstract description 2
229910052751 metal Chemical group 0.000 abstract description 2
239000002184 metal Chemical group 0.000 abstract description 2
238000009833 condensation Methods 0.000 abstract 2
230000005494 condensation Effects 0.000 abstract 2
BHESZOICBTWRPK-UHFFFAOYSA-N 4-[1-[1-(2h-triazol-4-yl)ethoxy]ethyl]-2h-triazole Chemical class C=1NN=NC=1C(C)OC(C)C1=CNN=N1 BHESZOICBTWRPK-UHFFFAOYSA-N 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
241000196324 Embryophyta Species 0.000 description 28
239000013543 active substance Substances 0.000 description 12
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
239000007921 spray Substances 0.000 description 11
241000233866 Fungi Species 0.000 description 10
OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
206010061217 Infestation Diseases 0.000 description 8
239000000460 chlorine Substances 0.000 description 8
240000005979 Hordeum vulgare Species 0.000 description 7
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 7
239000000843 powder Substances 0.000 description 7
239000002904 solvent Substances 0.000 description 7
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
238000009472 formulation Methods 0.000 description 6
239000000243 solution Substances 0.000 description 6
235000013399 edible fruits Nutrition 0.000 description 5
208000015181 infectious disease Diseases 0.000 description 5
244000005700 microbiome Species 0.000 description 5
239000000725 suspension Substances 0.000 description 5
239000005995 Aluminium silicate Substances 0.000 description 4
244000105624 Arachis hypogaea Species 0.000 description 4
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 4
241000220225 Malus Species 0.000 description 4
SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 4
241000221300 Puccinia Species 0.000 description 4
241000209140 Triticum Species 0.000 description 4
235000012211 aluminium silicate Nutrition 0.000 description 4
239000000969 carrier Substances 0.000 description 4
238000004440 column chromatography Methods 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
230000000694 effects Effects 0.000 description 4
NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 4
230000003032 phytopathogenic effect Effects 0.000 description 4
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
238000005160 1H NMR spectroscopy Methods 0.000 description 3
WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
241000221787 Erysiphe Species 0.000 description 3
206010017533 Fungal infection Diseases 0.000 description 3
235000007340 Hordeum vulgare Nutrition 0.000 description 3
208000031888 Mycoses Diseases 0.000 description 3
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
239000002202 Polyethylene glycol Substances 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
150000007513 acids Chemical class 0.000 description 3
235000021016 apples Nutrition 0.000 description 3
239000003054 catalyst Substances 0.000 description 3
239000012043 crude product Substances 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
239000000417 fungicide Substances 0.000 description 3
239000008187 granular material Substances 0.000 description 3
239000003208 petroleum Substances 0.000 description 3
229920001223 polyethylene glycol Polymers 0.000 description 3
229910002027 silica gel Inorganic materials 0.000 description 3
239000000741 silica gel Substances 0.000 description 3
239000002689 soil Substances 0.000 description 3
238000005507 spraying Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
125000001424 substituent group Chemical group 0.000 description 3
230000009885 systemic effect Effects 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
239000004563 wettable powder Substances 0.000 description 3
239000008096 xylene Substances 0.000 description 3
XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical group COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 2
235000001674 Agaricus brunnescens Nutrition 0.000 description 2
235000016068 Berberis vulgaris Nutrition 0.000 description 2
241000335053 Beta vulgaris Species 0.000 description 2
KZMGYPLQYOPHEL-UHFFFAOYSA-N Boron trifluoride etherate Chemical compound FB(F)F.CCOCC KZMGYPLQYOPHEL-UHFFFAOYSA-N 0.000 description 2
241000123650 Botrytis cinerea Species 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
229910021532 Calcite Inorganic materials 0.000 description 2
241001157813 Cercospora Species 0.000 description 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
240000008067 Cucumis sativus Species 0.000 description 2
AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 2
206010037888 Rash pustular Diseases 0.000 description 2
235000021307 Triticum Nutrition 0.000 description 2
150000001298 alcohols Chemical class 0.000 description 2
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
229910052784 alkaline earth metal Inorganic materials 0.000 description 2
238000004458 analytical method Methods 0.000 description 2
150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
125000003118 aryl group Chemical group 0.000 description 2
229960000892 attapulgite Drugs 0.000 description 2
239000004305 biphenyl Substances 0.000 description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 2
229910052794 bromium Inorganic materials 0.000 description 2
235000013339 cereals Nutrition 0.000 description 2
229910052801 chlorine Inorganic materials 0.000 description 2
239000003240 coconut oil Substances 0.000 description 2
235000019864 coconut oil Nutrition 0.000 description 2
239000012230 colorless oil Substances 0.000 description 2
239000012141 concentrate Substances 0.000 description 2
235000008504 concentrate Nutrition 0.000 description 2
238000005520 cutting process Methods 0.000 description 2
MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 2
238000006266 etherification reaction Methods 0.000 description 2
150000002170 ethers Chemical class 0.000 description 2
238000000605 extraction Methods 0.000 description 2
230000002349 favourable effect Effects 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
230000000855 fungicidal effect Effects 0.000 description 2
229910052736 halogen Inorganic materials 0.000 description 2
150000002367 halogens Chemical group 0.000 description 2
QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 2
238000011534 incubation Methods 0.000 description 2
229910052500 inorganic mineral Inorganic materials 0.000 description 2
150000002500 ions Chemical class 0.000 description 2
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
239000000463 material Substances 0.000 description 2
239000011707 mineral Substances 0.000 description 2
235000010755 mineral Nutrition 0.000 description 2
238000002156 mixing Methods 0.000 description 2
239000003921 oil Substances 0.000 description 2
235000019198 oils Nutrition 0.000 description 2
150000002924 oxiranes Chemical class 0.000 description 2
229910052625 palygorskite Inorganic materials 0.000 description 2
239000000546 pharmaceutical excipient Substances 0.000 description 2
239000000047 product Substances 0.000 description 2
208000029561 pustule Diseases 0.000 description 2
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
235000012239 silicon dioxide Nutrition 0.000 description 2
238000009331 sowing Methods 0.000 description 2
235000020354 squash Nutrition 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 2
DSSYKIVIOFKYAU-XCBNKYQSSA-N (R)-camphor Chemical compound C1C[C@@]2(C)C(=O)C[C@@H]1C2(C)C DSSYKIVIOFKYAU-XCBNKYQSSA-N 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
WKFFKUKOXXLUSL-UHFFFAOYSA-N 2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-methyloxirane Chemical compound C=1C=C(OC=2C=CC(Cl)=CC=2)C=C(Cl)C=1C1(C)CO1 WKFFKUKOXXLUSL-UHFFFAOYSA-N 0.000 description 1
PXACTUVBBMDKRW-UHFFFAOYSA-N 4-bromobenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=C(Br)C=C1 PXACTUVBBMDKRW-UHFFFAOYSA-N 0.000 description 1
UHPMCKVQTMMPCG-UHFFFAOYSA-N 5,8-dihydroxy-2-methoxy-6-methyl-7-(2-oxopropyl)naphthalene-1,4-dione Chemical compound CC1=C(CC(C)=O)C(O)=C2C(=O)C(OC)=CC(=O)C2=C1O UHPMCKVQTMMPCG-UHFFFAOYSA-N 0.000 description 1
244000291564 Allium cepa Species 0.000 description 1
235000002732 Allium cepa var. cepa Nutrition 0.000 description 1
241000223600 Alternaria Species 0.000 description 1
244000144725 Amygdalus communis Species 0.000 description 1
241000235349 Ascomycota Species 0.000 description 1
244000003416 Asparagus officinalis Species 0.000 description 1
235000005340 Asparagus officinalis Nutrition 0.000 description 1
235000007319 Avena orientalis Nutrition 0.000 description 1
244000075850 Avena orientalis Species 0.000 description 1
241001480061 Blumeria graminis Species 0.000 description 1
241001465180 Botrytis Species 0.000 description 1
241000167854 Bourreria succulenta Species 0.000 description 1
244000056139 Brassica cretica Species 0.000 description 1
235000003351 Brassica cretica Nutrition 0.000 description 1
240000002791 Brassica napus Species 0.000 description 1
240000007124 Brassica oleracea Species 0.000 description 1
235000003899 Brassica oleracea var acephala Nutrition 0.000 description 1
235000011301 Brassica oleracea var capitata Nutrition 0.000 description 1
235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 1
235000003343 Brassica rupestris Nutrition 0.000 description 1
235000004977 Brassica sinapistrum Nutrition 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
244000025254 Cannabis sativa Species 0.000 description 1
235000012766 Cannabis sativa ssp. sativa var. sativa Nutrition 0.000 description 1
235000012765 Cannabis sativa ssp. sativa var. spontanea Nutrition 0.000 description 1
235000002566 Capsicum Nutrition 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
241000723346 Cinnamomum camphora Species 0.000 description 1
235000005979 Citrus limon Nutrition 0.000 description 1
244000131522 Citrus pyriformis Species 0.000 description 1
241001672694 Citrus reticulata Species 0.000 description 1
240000000560 Citrus x paradisi Species 0.000 description 1
235000013162 Cocos nucifera Nutrition 0.000 description 1
244000060011 Cocos nucifera Species 0.000 description 1
240000007154 Coffea arabica Species 0.000 description 1
240000000491 Corchorus aestuans Species 0.000 description 1
235000011777 Corchorus aestuans Nutrition 0.000 description 1
235000010862 Corchorus capsularis Nutrition 0.000 description 1
229920000742 Cotton Polymers 0.000 description 1
241000219112 Cucumis Species 0.000 description 1
235000015510 Cucumis melo subsp melo Nutrition 0.000 description 1
235000009849 Cucumis sativus Nutrition 0.000 description 1
235000009854 Cucurbita moschata Nutrition 0.000 description 1
240000001980 Cucurbita pepo Species 0.000 description 1
235000009852 Cucurbita pepo Nutrition 0.000 description 1
241000371644 Curvularia ravenelii Species 0.000 description 1
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
235000002767 Daucus carota Nutrition 0.000 description 1
244000000626 Daucus carota Species 0.000 description 1
MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 1
101100310856 Drosophila melanogaster spri gene Proteins 0.000 description 1
241000221785 Erysiphales Species 0.000 description 1
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 1
240000009088 Fragaria x ananassa Species 0.000 description 1
241000223218 Fusarium Species 0.000 description 1
235000010469 Glycine max Nutrition 0.000 description 1
244000068988 Glycine max Species 0.000 description 1
244000299507 Gossypium hirsutum Species 0.000 description 1
241000208818 Helianthus Species 0.000 description 1
235000003222 Helianthus annuus Nutrition 0.000 description 1
241001181537 Hemileia Species 0.000 description 1
244000043261 Hevea brasiliensis Species 0.000 description 1
235000008694 Humulus lupulus Nutrition 0.000 description 1
244000025221 Humulus lupulus Species 0.000 description 1
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 1
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
235000003228 Lactuca sativa Nutrition 0.000 description 1
240000008415 Lactuca sativa Species 0.000 description 1
241000218195 Lauraceae Species 0.000 description 1
240000004322 Lens culinaris Species 0.000 description 1
235000014647 Lens culinaris subsp culinaris Nutrition 0.000 description 1
239000002841 Lewis acid Substances 0.000 description 1
235000004431 Linum usitatissimum Nutrition 0.000 description 1
240000006240 Linum usitatissimum Species 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
244000081841 Malus domestica Species 0.000 description 1
239000012359 Methanesulfonyl chloride Substances 0.000 description 1
241001518729 Monilinia Species 0.000 description 1
240000005561 Musa balbisiana Species 0.000 description 1
235000018290 Musa x paradisiaca Nutrition 0.000 description 1
235000002637 Nicotiana tabacum Nutrition 0.000 description 1
244000061176 Nicotiana tabacum Species 0.000 description 1
241000207836 Olea <angiosperm> Species 0.000 description 1
240000007594 Oryza sativa Species 0.000 description 1
235000007164 Oryza sativa Nutrition 0.000 description 1
240000001090 Papaver somniferum Species 0.000 description 1
235000008753 Papaver somniferum Nutrition 0.000 description 1
241000315044 Passalora arachidicola Species 0.000 description 1
244000025272 Persea americana Species 0.000 description 1
235000008673 Persea americana Nutrition 0.000 description 1
235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
244000046052 Phaseolus vulgaris Species 0.000 description 1
241000758706 Piperaceae Species 0.000 description 1
235000010582 Pisum sativum Nutrition 0.000 description 1
240000004713 Pisum sativum Species 0.000 description 1
241000896242 Podosphaera Species 0.000 description 1
240000005809 Prunus persica Species 0.000 description 1
235000006040 Prunus persica var persica Nutrition 0.000 description 1
241000221301 Puccinia graminis Species 0.000 description 1
241000221535 Pucciniales Species 0.000 description 1
241000220324 Pyrus Species 0.000 description 1
241001361634 Rhizoctonia Species 0.000 description 1
235000004443 Ricinus communis Nutrition 0.000 description 1
240000007651 Rubus glaucus Species 0.000 description 1
240000000111 Saccharum officinarum Species 0.000 description 1
235000007201 Saccharum officinarum Nutrition 0.000 description 1
206010039509 Scab Diseases 0.000 description 1
235000007238 Secale cereale Nutrition 0.000 description 1
244000082988 Secale cereale Species 0.000 description 1
239000004113 Sepiolite Substances 0.000 description 1
241001533598 Septoria Species 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
235000002595 Solanum tuberosum Nutrition 0.000 description 1
244000061456 Solanum tuberosum Species 0.000 description 1
235000009337 Spinacia oleracea Nutrition 0.000 description 1
244000300264 Spinacia oleracea Species 0.000 description 1
244000269722 Thea sinensis Species 0.000 description 1
244000299461 Theobroma cacao Species 0.000 description 1
235000009470 Theobroma cacao Nutrition 0.000 description 1
241000510929 Uncinula Species 0.000 description 1
244000078534 Vaccinium myrtillus Species 0.000 description 1
241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
241000228452 Venturia inaequalis Species 0.000 description 1
241000219094 Vitaceae Species 0.000 description 1
208000027418 Wounds and injury Diseases 0.000 description 1
240000008042 Zea mays Species 0.000 description 1
235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
235000002017 Zea mays subsp mays Nutrition 0.000 description 1
IIHVTSVMDGLABU-UHFFFAOYSA-N [2-[2-chloro-4-(4-chlorophenoxy)phenyl]-2-methoxypropyl] methanesulfonate Chemical compound C1=C(Cl)C(C(C)(COS(C)(=O)=O)OC)=CC=C1OC1=CC=C(Cl)C=C1 IIHVTSVMDGLABU-UHFFFAOYSA-N 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002378 acidificating effect Effects 0.000 description 1
125000004423 acyloxy group Chemical group 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000000853 adhesive Substances 0.000 description 1
230000001070 adhesive effect Effects 0.000 description 1
230000000274 adsorptive effect Effects 0.000 description 1
230000002411 adverse Effects 0.000 description 1
239000003905 agrochemical Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
235000020224 almond Nutrition 0.000 description 1
239000003945 anionic surfactant Substances 0.000 description 1
230000000844 anti-bacterial effect Effects 0.000 description 1
125000004429 atom Chemical group 0.000 description 1
239000003899 bactericide agent Substances 0.000 description 1
239000000440 bentonite Substances 0.000 description 1
229910000278 bentonite Inorganic materials 0.000 description 1
SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
SRSXLGNVWSONIS-UHFFFAOYSA-N benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-N 0.000 description 1
229940092714 benzenesulfonic acid Drugs 0.000 description 1
235000021028 berry Nutrition 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
235000021029 blackberry Nutrition 0.000 description 1
238000009835 boiling Methods 0.000 description 1
239000011449 brick Substances 0.000 description 1
230000001680 brushing effect Effects 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
229960000846 camphor Drugs 0.000 description 1
229930008380 camphor Natural products 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
239000004359 castor oil Substances 0.000 description 1
235000019438 castor oil Nutrition 0.000 description 1
125000002091 cationic group Chemical group 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
238000006243 chemical reaction Methods 0.000 description 1
239000007795 chemical reaction product Substances 0.000 description 1
235000019693 cherries Nutrition 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
235000016213 coffee Nutrition 0.000 description 1
235000013353 coffee beverage Nutrition 0.000 description 1
239000002131 composite material Substances 0.000 description 1
238000001816 cooling Methods 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
230000006378 damage Effects 0.000 description 1
239000003599 detergent Substances 0.000 description 1
DOIRQSBPFJWKBE-UHFFFAOYSA-N dibutyl phthalate Chemical group CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000010410 dusting Methods 0.000 description 1
239000003480 eluent Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
230000001804 emulsifying effect Effects 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
238000005516 engineering process Methods 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
229910052731 fluorine Inorganic materials 0.000 description 1
239000011737 fluorine Substances 0.000 description 1
238000001640 fractional crystallisation Methods 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
150000002334 glycols Chemical class 0.000 description 1
235000021021 grapes Nutrition 0.000 description 1
238000000227 grinding Methods 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
239000011487 hemp Substances 0.000 description 1
239000004009 herbicide Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
208000014674 injury Diseases 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
235000021374 legumes Nutrition 0.000 description 1
150000007517 lewis acids Chemical class 0.000 description 1
230000000670 limiting effect Effects 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
QARBMVPHQWIHKH-UHFFFAOYSA-N methanesulfonyl chloride Chemical compound CS(Cl)(=O)=O QARBMVPHQWIHKH-UHFFFAOYSA-N 0.000 description 1
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
239000003750 molluscacide Substances 0.000 description 1
230000002013 molluscicidal effect Effects 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
YZMHQCWXYHARLS-UHFFFAOYSA-N naphthalene-1,2-disulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(S(=O)(=O)O)=CC=C21 YZMHQCWXYHARLS-UHFFFAOYSA-N 0.000 description 1
150000002790 naphthalenes Chemical class 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
230000003287 optical effect Effects 0.000 description 1
235000020232 peanut Nutrition 0.000 description 1
235000021017 pears Nutrition 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
150000003021 phthalic acid derivatives Chemical class 0.000 description 1
230000000704 physical effect Effects 0.000 description 1
230000008635 plant growth Effects 0.000 description 1
235000021018 plums Nutrition 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
230000003449 preventive effect Effects 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
239000008262 pumice Substances 0.000 description 1
235000021013 raspberries Nutrition 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000002829 reductive effect Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
239000011833 salt mixture Substances 0.000 description 1
239000004576 sand Substances 0.000 description 1
238000000926 separation method Methods 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
159000000000 sodium salts Chemical class 0.000 description 1
235000012424 soybean oil Nutrition 0.000 description 1
239000003549 soybean oil Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000004575 stone Substances 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
235000013616 tea Nutrition 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
238000004809 thin layer chromatography Methods 0.000 description 1
239000011573 trace mineral Substances 0.000 description 1
235000013619 trace mineral Nutrition 0.000 description 1
ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 1
125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
235000013311 vegetables Nutrition 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000000080 wetting agent Substances 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C309/00—Sulfonic acids; Halides, esters, or anhydrides thereof
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/14—Unsaturated ethers
- C07C43/178—Unsaturated ethers containing hydroxy or O-metal groups
- C07C43/1782—Unsaturated ethers containing hydroxy or O-metal groups containing six-membered aromatic rings
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles

Landscapes

Organic Chemistry (AREA)
Chemical & Material Sciences (AREA)
Life Sciences & Earth Sciences (AREA)
Dentistry (AREA)
Engineering & Computer Science (AREA)
Plant Pathology (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Health & Medical Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Plural Heterocyclic Compounds (AREA)
Epoxy Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Nitrogen Condensed Heterocyclic Rings (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Saccharide Compounds (AREA)

DD84281418A 1983-05-19 1984-05-17 Mikrobizides mittel DD248274A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
CH273083		1983-05-19

Publications (1)

Publication Number	Publication Date
DD248274A5 true DD248274A5 (de)	1987-08-05

Family

ID=4240315

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
DD84263132A DD226882A5 (de)	1983-05-19	1984-05-17	Verfahren zur herstellung von 1-triazolylethylether-derivaten
DD84281418A DD248274A5 (de)	1983-05-19	1984-05-17	Mikrobizides mittel

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
DD84263132A DD226882A5 (de)	1983-05-19	1984-05-17	Verfahren zur herstellung von 1-triazolylethylether-derivaten

Country Status (25)

Country	Link
US (1)	US4945100A (fr)
EP (1)	EP0126430B1 (fr)
JP (3)	JPS59222434A (fr)
KR (2)	KR890000533B1 (fr)
AT (1)	ATE66676T1 (fr)
AU (2)	AU572145B2 (fr)
BR (1)	BR8402388A (fr)
CA (1)	CA1223264A (fr)
CS (2)	CS247179B2 (fr)
DD (2)	DD226882A5 (fr)
DE (1)	DE3484968D1 (fr)
DK (1)	DK248184A (fr)
ES (1)	ES8600635A1 (fr)
GB (2)	GB2143815B (fr)
GR (1)	GR79954B (fr)
HU (1)	HU196693B (fr)
IE (2)	IE57488B1 (fr)
IL (3)	IL83707A (fr)
MX (1)	MX5769A (fr)
MY (1)	MY102774A (fr)
NZ (2)	NZ219282A (fr)
PH (3)	PH20959A (fr)
PT (1)	PT78602A (fr)
TR (1)	TR22379A (fr)
ZA (1)	ZA843774B (fr)

Families Citing this family (75)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
EP0126430B1 (fr) *	1983-05-19	1991-08-28	Ciba-Geigy Ag	Procédé pour la préparation de dérivés de 1-triazolyléthyléthers, composés microbicides contenant des dérivés nouveaux de 1-triazolyl-phenoxyphényléthyléther comme ingrédients actifs et leur application
EP0158448B1 (fr) *	1984-04-05	1990-08-29	Imperial Chemical Industries Plc	Azolylpropanols
EP0223327B1 (fr) *	1985-08-07	1991-10-16	Imperial Chemical Industries Plc	Dérivés de triazolylméthyl-tert.-butyl-carbinol, leurs procédés de préparation et leur utilisation comme régulateurs de croissance des plantes
GB8603951D0 (en) *	1986-02-18	1986-03-26	Ici Plc	Heterocyclic compounds
EP0275955B1 (fr) *	1987-01-21	1990-07-04	Ciba-Geigy Ag	Composition microbicide
DE3732387A1 (de) *	1987-09-25	1989-04-06	Bayer Ag	Azolylmethylcyclopropyl-derivate enthaltende antimykotische mittel
DE58903329D1 (de) *	1988-08-04	1993-03-04	Ciba Geigy Ag	Mikrobizide mittel.
US4940720A (en) *	1989-08-02	1990-07-10	Ciba-Geigy Corporation	Microbicidal compositions
US5358939A (en) *	1992-06-25	1994-10-25	Rohm And Haas Company	Fungicidal 2-aryl-2,2-disubstituted ethyl-1,2,4-triazoles
NZ270418A (en)	1994-02-07	1997-09-22	Eisai Co Ltd	Polycyclic triazole & imidazole derivatives, antifungal compositions
KR20020037652A (ko) *	2000-11-15	2002-05-22	김응필	비중분리 선광기
JP5260540B2 (ja)	2006-11-22	2013-08-14	ビーエーエスエフソシエタス・ヨーロピア	液体水性農芸化学製剤
PL2184993T3 (pl)	2007-08-08	2012-03-30	Basf Se	Wodne mikroemulsje zawierające owadobójcze związki organiczne
CN102105052A (zh) *	2008-07-24	2011-06-22	巴斯夫欧洲公司	包含溶剂、水、表面活性剂和农药的水包油乳液
TW201018400A (en)	2008-10-10	2010-05-16	Basf Se	Liquid aqueous plant protection formulations
UA106213C2 (ru)	2008-10-10	2014-08-11	Басф Се	Жидкие препараты для защиты растений, содержащие пираклостробин
PE20140826A1 (es)	2011-07-13	2014-07-09	Basf Se	Compuestos sustituidos fungicidas de 2-[2-halogenalquil-4-(fenoxi)-fenil]-1-[1,2,4]triazol-1-il-etanol
EP2731438B1 (fr)	2011-07-15	2015-04-08	Basf Se	Composés fongicides alkyl-substitués 2-[2-chloro-4-(4-chloro-phénoxy)-phényl]-1-[1,2,4]triazol-1 yl-éthanol
BR112014000538A2 (pt) *	2011-07-15	2016-08-23	Basf Se	compostos, processo para a preparação dos compostos, composições agroquímicas, utilização dos compostos e semente revestida
JP2014520833A (ja)	2011-07-15	2014-08-25	ビーエーエスエフソシエタス・ヨーロピア	殺菌性フェニルアルキル−置換２−［２−クロロ−４−（４−クロロ−フェノキシ）−フェニル］−１−［１，２，４］トリアゾール−１−イル−エタノール化合物
EP2559688A1 (fr)	2011-08-15	2013-02-20	Basf Se	Composés de 1-{2-[2-halo-4-(4-halogène-phénoxy)-phényl]-2-butoxy-éthyl}-1h [1,2,4]triazole substitués fongicides
PE20141393A1 (es)	2011-08-15	2014-10-22	Basf Se	Compuestos fungicidas de 1-{2-[2-halo-4-(4-halogen-fenoxi)-fenil]-2-aluiniloxi-etil}-1h-[1,2,4] triazol sustituidos
EP2744794B1 (fr) *	2011-08-15	2015-12-30	Basf Se	Composés de 1-{2-cyclyloxy-2-[2-halo-4-(4-halogène-phénoxy)-phényl]-éthyl}-1h-[1,2,4]triazole substitués fongicides
JP2014525407A (ja)	2011-08-15	2014-09-29	ビーエーエスエフソシエタス・ヨーロピア	殺菌性置換１−｛２−［２−ハロ−４−（４−ハロゲン−フェノキシ）−フェニル］−２−アルコキシ−２−アルキニル／アルケニル−エチル｝−１ｈ−［１，２，４］トリアゾール化合物
JP2014524431A (ja)	2011-08-15	2014-09-22	ビーエーエスエフソシエタス・ヨーロピア	殺菌性置換１−｛２−［２−ハロ−４−（４−ハロゲン−フェノキシ）−フェニル］−２−アルコキシ−ヘキシル｝−１ｈ−［１，２，４］トリアゾール化合物
EP2744791B1 (fr)	2011-08-15	2015-10-28	Basf Se	Composés de 1-{2-[2-halogéno-4-(4-halogéno-phénoxy)-phényl]-2-alcoxy-3-méthyl-butyl}-1h-[1,2,4]triazole substitués fongicides
AR087535A1 (es) *	2011-08-15	2014-04-03	Basf Se	Compuestos fungicidas de 1-{2-[2-halo-4-(4-halogen-fenoxi)-fenil]-2-etoxi-etil}-1h-[1,2,4]triazol sustituidos
BR112014002499A2 (pt) *	2011-08-15	2017-02-21	Basf Se	compostos, processos para a preparação de compostos de fórmula i, composições agroquímicas e usos de compostos de fórmula i ou viii
US9752105B2 (en)	2012-09-13	2017-09-05	Ecolab Usa Inc.	Two step method of cleaning, sanitizing, and rinsing a surface
US20140308162A1 (en)	2013-04-15	2014-10-16	Ecolab Usa Inc.	Peroxycarboxylic acid based sanitizing rinse additives for use in ware washing
WO2014082879A1 (fr)	2012-11-27	2014-06-05	Basf Se	Composés de [1,2,4]triazole substitués
BR112015012003A2 (pt) *	2012-11-27	2018-05-15	Basf Se	compostos de fórmula i, composição, utilização de um composto, método para o combate dos fungos nocivos, semente, processo para a preparação dos compostos e compostos intermediários
EP2735563A1 (fr) *	2012-11-27	2014-05-28	Basf Se	Composés méta substitués de 2-[phénoxy-phényl]-1-[1,2,4]triazol-1-yl-éthanol et leur utilisation en tant que fongicides
WO2014082871A1 (fr)	2012-11-27	2014-06-05	Basf Se	Composés de 2-[phénoxyphényl]-1-[1,2,4]triazol-1-yl-éthanol substitués et leur utilisation comme fongicides
US20160029630A1 (en)	2012-11-27	2016-02-04	Basf Se	Substituted 2-[phenoxy-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds and their use as fungicides
US20150313229A1 (en)	2012-11-27	2015-11-05	Basf Se	Substituted [1,2,4] Triazole Compounds
WO2014095548A1 (fr) *	2012-12-19	2014-06-26	Basf Se	Composés triazoles substitués en [1,2,4] et leur utilisation comme fongicides
BR112015014753B8 (pt)	2012-12-20	2020-03-03	Basf Agro Bv	composições, uso de uma composição, método para o combate de fungos fitopatogênicos e uso dos componentes
CN104936450A (zh) *	2012-12-20	2015-09-23	巴斯夫欧洲公司	包含三唑化合物的组合物
US20150351399A1 (en) *	2013-01-09	2015-12-10	Basf Se	Substituted [1,2,4]triazole and imidazole compounds
UA122520C2 (uk)	2013-01-09	2020-11-25	Басф Агро Б.В.	Кристалічна форма 2-[4-(4-хлорфенокси)-2-(трифторметил)феніл]-1-(1,2,4-триазол-1-іл)пропан-2-олу, агрохімічна композиція, застосування та спосіб боротьби зі шкідливими грибами
WO2014124850A1 (fr)	2013-02-14	2014-08-21	Basf Se	Composés [1,2,4]triazole et imidazole substitués
WO2014198553A1 (fr) *	2013-06-12	2014-12-18	Basf Se	Composés imidazole et triazole [1,2,4]substitués
EP2813499A1 (fr)	2013-06-12	2014-12-17	Basf Se	Composés de [1,2,4]triazole et d'imidazole substitués
WO2014198557A1 (fr) *	2013-06-12	2014-12-18	Basf Se	Composés imidazole et triazole [1,2,4] substitués
WO2015003908A1 (fr) *	2013-07-08	2015-01-15	Basf Se	Compositions comprenant un composé triazole et un biopesticide
EP2839745A1 (fr)	2013-08-21	2015-02-25	Basf Se	Formulations agrochimiques comprenant un 2-éthyl-hexanol alkoxylat
JP6053948B2 (ja)	2013-10-24	2016-12-27	三菱電機株式会社	情報処理装置及び情報処理方法及びプログラム
CN106170205B (zh)	2014-02-14	2020-01-17	巴斯夫农业公司	包含农药、脂肪酰胺和乳酰胺的可乳化浓缩物
EA201892682A1 (ru)	2014-06-25	2019-04-30	Басф Агро Б.В.	Пестицидные композиции
DK3166932T3 (en)	2014-07-08	2018-10-01	Basf Agro Bv	PROCEDURE FOR PREPARING SUBSTITUTED OXIRANES AND TRIAZOLES
UA120058C2 (uk)	2014-07-14	2019-09-25	Басф Се	Пестицидні композиції
PL3214937T3 (pl)	2014-11-07	2024-10-14	Basf Se	Mieszaniny szkodnikobójcze
EP3028573A1 (fr)	2014-12-05	2016-06-08	Basf Se	Utilisation d'un triazole fongicide sur des plantes transgéniques
WO2016174042A1 (fr)	2015-04-27	2016-11-03	BASF Agro B.V.	Compositions pesticides
EP3294720B1 (fr)	2015-05-08	2020-12-02	BASF Agro B.V.	Procédé de préparation du terpinolène époxyde
DK3294700T3 (da)	2015-05-08	2020-04-14	Basf Agro Bv	Fremgangsmåde til fremstilling af limonen-4-ol
PL3316692T3 (pl)	2015-07-02	2021-10-11	BASF Agro B.V.	Kompozycje owadobójcze zawierające związek triazolowy
EP3111763A1 (fr)	2015-07-02	2017-01-04	BASF Agro B.V.	Compositions pesticides comprenant un composé de triazole
RU2754614C2 (ru)	2016-03-16	2021-09-03	Басф Се	Применение тетразолинонов для борьбы с устойчивыми фитопатогенными грибами на злаковых культурах
WO2017157920A1 (fr)	2016-03-16	2017-09-21	Basf Se	Utilisation de tétrazolinones pour lutter contre des champignons phytopathogènes résistants sur des fruits
BR112018068705B1 (pt)	2016-03-16	2022-09-06	Basf Se	Método para controlar fungos fitopatogênicos
EP3472139B1 (fr)	2016-06-15	2021-04-07	BASF Agro B.V.	Procédé d'époxydation d'un alcène tétrasubstitué
ES2833202T3 (es)	2016-06-15	2021-06-14	Basf Agro Bv	Procedimiento para la epoxidación de un alqueno tetrasustituido
CN109715622A (zh)	2016-09-22	2019-05-03	拜耳作物科学股份公司	新的三唑衍生物及其作为杀真菌剂的用途
EP3515907A1 (fr)	2016-09-22	2019-07-31	Bayer CropScience Aktiengesellschaft	Nouveaux dérivés triazole
US20200045967A1 (en)	2017-02-08	2020-02-13	Bayer Cropscience Aktiengesellschaft	Novel triazole derivatives
CA3052519A1 (fr)	2017-02-08	2018-08-16	Andreas Gortz	Derives de triazolethione
BR112019016241A2 (pt)	2017-02-08	2020-04-07	Bayer Cropscience Ag	derivados de triazol e seu uso como fungicidas
KR20190115449A (ko)	2017-02-10	2019-10-11	바이엘 악티엔게젤샤프트	1-(페녹시-피리디닐)-2-(1,2,4-트리아졸-1-일)-에탄올 유도체를 포함하는 유해 미생물을 방제하기 위한 조성물
EP3421460A1 (fr)	2018-03-15	2019-01-02	Bayer Aktiengesellschaft	Fongicides de 2-[(4-alkylphenoxy)-pyridinyl]-1-(1,2,4-triazol-1-yl)alkan-2-ol
WO2020020813A1 (fr)	2018-07-25	2020-01-30	Bayer Aktiengesellschaft	Combinaisons de composés actifs fongicides
WO2020020816A1 (fr)	2018-07-26	2020-01-30	Bayer Aktiengesellschaft	Nouveaux dérivés de triazole
WO2020070050A1 (fr)	2018-10-01	2020-04-09	Bayer Aktiengesellschaft	Dérivés d'imidazol-1-yl carbinol substitués en position 5 servant de fongicides
EP3620053A1 (fr)	2018-12-14	2020-03-11	Bayer Aktiengesellschaft	Combinaisons de composés actifs des fongicides

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE2547953A1 (de) *	1975-10-27	1977-04-28	Bayer Ag	(1-phenyl-2-triazolyl-aethyl)-aether- derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
AU515134B2 (en) *	1976-08-10	1981-03-19	Janssen Pharmaceutica N.V.	1-(2-aryl-2-r-ethyl)-1h-1,2,4-triazoles
DE2650831A1 (de) *	1976-11-06	1978-05-11	Basf Ag	Mittel zur beeinflussung des pflanzenwachstums
DE2725214A1 (de) *	1977-06-03	1978-12-14	Bayer Ag	Metallsalzkomplexe von 1-phenyl-2- triazolyl-aethyl-derivaten, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide
DE2725314A1 (de) *	1977-06-04	1978-12-14	Bayer Ag	1-(2-phenylaethyl)-triazolium-salze, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide
US4654332A (en) *	1979-03-07	1987-03-31	Imperial Chemical Industries Plc	Heterocyclic compounds
CH647513A5 (de) *	1979-11-13	1985-01-31	Sandoz Ag	Triazol-derivate, deren herstellung und verwendung.
AU542623B2 (en) *	1980-05-16	1985-02-28	Bayer Aktiengesellschaft	1-hydroxyethyl-azole derivatives
EP0131684B1 (fr) *	1980-08-18	1992-03-11	Imperial Chemical Industries Plc	Utilization des dérivés de triazolyléthanols et leurs compositions comme fongicides en dehors de l'agriculture
EP0158741A3 (fr) *	1980-11-19	1986-02-12	Imperial Chemical Industries Plc	Intermédiaires pour composés fongicides triazoles ou imidazoles
DE3140276A1 (de) *	1981-10-10	1983-04-28	Bayer Ag, 5090 Leverkusen	Phenoxyphenyl-azolylmethyl-ketone und -carbinole, verfahren zu ihrer herstellung und ihre verwendung als fungizide und als zwischenprodukte
DE3280075D1 (de) *	1981-11-27	1990-02-08	Ciba Geigy Ag	Mikrobizide triazolyl-ethyl-aether.
DE3202604A1 (de) *	1982-01-27	1983-08-04	Bayer Ag, 5090 Leverkusen	Ether-derivate von substituierten 1-hydroxyalkyl-azolen, verfahren zu ihrer herstellung sowie ihre verwendung als fungizide und pflanzenwachstumsregulatoren
US4610716A (en) *	1982-12-14	1986-09-09	Ciba-Geigy Corporation	Fluorinated azolyl ethanol growth regulators and microbicides
EP0126430B1 (fr) *	1983-05-19	1991-08-28	Ciba-Geigy Ag	Procédé pour la préparation de dérivés de 1-triazolyléthyléthers, composés microbicides contenant des dérivés nouveaux de 1-triazolyl-phenoxyphényléthyléther comme ingrédients actifs et leur application

1984
- 1984-05-16 EP EP84105582A patent/EP0126430B1/fr not_active Expired - Lifetime
- 1984-05-16 AT AT84105582T patent/ATE66676T1/de active
- 1984-05-16 GB GB08412506A patent/GB2143815B/en not_active Expired
- 1984-05-16 DE DE8484105582T patent/DE3484968D1/de not_active Expired - Lifetime
- 1984-05-17 IL IL8483707A patent/IL83707A/xx unknown
- 1984-05-17 IL IL71862A patent/IL71862A/xx unknown
- 1984-05-17 CA CA000454548A patent/CA1223264A/fr not_active Expired
- 1984-05-17 GR GR74745A patent/GR79954B/el unknown
- 1984-05-17 DD DD84263132A patent/DD226882A5/de not_active IP Right Cessation
- 1984-05-17 PT PT78602A patent/PT78602A/pt not_active IP Right Cessation
- 1984-05-17 DK DK248184A patent/DK248184A/da not_active Application Discontinuation
- 1984-05-17 DD DD84281418A patent/DD248274A5/de not_active IP Right Cessation
- 1984-05-18 IE IE1247/84A patent/IE57488B1/en not_active IP Right Cessation
- 1984-05-18 TR TR3611/84A patent/TR22379A/xx unknown
- 1984-05-18 MX MX576984A patent/MX5769A/es unknown
- 1984-05-18 NZ NZ219282A patent/NZ219282A/en unknown
- 1984-05-18 IE IE2779/88A patent/IE57489B1/en not_active IP Right Cessation
- 1984-05-18 CS CS843769A patent/CS247179B2/cs unknown
- 1984-05-18 ZA ZA843774A patent/ZA843774B/xx unknown
- 1984-05-18 ES ES532604A patent/ES8600635A1/es not_active Expired
- 1984-05-18 PH PH30696A patent/PH20959A/en unknown
- 1984-05-18 NZ NZ208209A patent/NZ208209A/en unknown
- 1984-05-18 HU HU841926A patent/HU196693B/hu not_active IP Right Cessation
- 1984-05-18 BR BR8402388A patent/BR8402388A/pt not_active IP Right Cessation
- 1984-05-18 AU AU28358/84A patent/AU572145B2/en not_active Ceased
- 1984-05-19 KR KR1019840002741A patent/KR890000533B1/ko not_active Expired
- 1984-05-19 JP JP59101625A patent/JPS59222434A/ja active Granted
1985
- 1985-08-08 CS CS855782A patent/CS247200B2/cs unknown
- 1985-10-25 PH PH32973A patent/PH21667A/en unknown
- 1985-10-25 PH PH32974A patent/PH22876A/en unknown
1986
- 1986-09-22 GB GB08622763A patent/GB2179659B/en not_active Expired
1987
- 1987-08-31 IL IL83707A patent/IL83707A0/xx unknown
- 1987-09-30 MY MYPI87002496A patent/MY102774A/en unknown
1988
- 1988-05-02 AU AU15504/88A patent/AU607993B2/en not_active Ceased
- 1988-09-02 US US07/240,441 patent/US4945100A/en not_active Expired - Fee Related
- 1988-11-10 KR KR1019880014855A patent/KR900003367B1/ko not_active Expired
1989
- 1989-05-01 JP JP1112793A patent/JPH0296544A/ja active Granted
- 1989-05-01 JP JP1112794A patent/JPH0285265A/ja active Granted

Also Published As

Publication number	Publication date
HUT34011A (en)	1985-01-28
IL83707A0 (en)	1988-01-31
JPH0361666B2 (fr)	1991-09-20
DD226882A5 (de)	1985-09-04
JPH0285265A (ja)	1990-03-26
TR22379A (tr)	1987-03-11
DE3484968D1 (de)	1991-10-02
PH20959A (en)	1987-06-10
IL71862A (en)	1988-08-31
GB2143815A (en)	1985-02-20
KR890000533B1 (ko)	1989-03-20
JPS59222434A (ja)	1984-12-14
EP0126430A2 (fr)	1984-11-28
JPH0552819B2 (fr)	1993-08-06
ES532604A0 (es)	1985-10-16
HU196693B (en)	1989-01-30
US4945100A (en)	1990-07-31
DK248184A (da)	1984-11-20
IE57488B1 (en)	1992-10-07
KR900003367B1 (ko)	1990-05-16
IE57489B1 (en)	1992-10-07
JPH0420912B2 (fr)	1992-04-07
JPH0296544A (ja)	1990-04-09
IL71862A0 (en)	1984-09-30
IE841247L (en)	1984-11-19
GR79954B (fr)	1984-10-31
GB8412506D0 (en)	1984-06-20
AU2835884A (en)	1984-11-22
IE882779L (en)	1984-11-19
ZA843774B (en)	1985-01-30
CA1223264A (fr)	1987-06-23
IL83707A (en)	1988-08-31
AU572145B2 (en)	1988-05-05
GB2179659B (en)	1988-01-27
PT78602A (de)	1984-06-01
AU1550488A (en)	1988-07-21
NZ208209A (en)	1988-01-08
PH21667A (en)	1988-01-13
GB2143815B (en)	1988-01-20
AU607993B2 (en)	1991-03-21
ES8600635A1 (es)	1985-10-16
EP0126430A3 (en)	1986-05-14
ATE66676T1 (de)	1991-09-15
DK248184D0 (da)	1984-05-17
EP0126430B1 (fr)	1991-08-28
GB2179659A (en)	1987-03-11
GB8622763D0 (en)	1986-10-29
MX5769A (es)	1993-10-01
KR900008926A (ko)	1990-06-03
CS247200B2 (cs)	1986-12-18
BR8402388A (pt)	1985-04-02
MY102774A (en)	1992-10-31
CS247179B2 (en)	1986-12-18
PH22876A (en)	1989-01-19
KR850000417A (ko)	1985-02-27
NZ219282A (en)	1988-02-12

Legal Events

Date	Code	Title	Description
1995-08-31	ENJ	Ceased due to non-payment of renewal fee

Publication	Publication Date	Title
DD248274A5 (de)	1987-08-05	Mikrobizides mittel
EP0065485B1 (fr)	1990-04-18	Dérivés d'arylphényléthers comme microbicide, procédé pour leur préparation et leur application
EP0275955B1 (fr)	1990-07-04	Composition microbicide
EP0113640B1 (fr)	1990-05-23	1-Azolyl-2-aryl-3-fluoralcane-2-ols microbicides
EP0114567B1 (fr)	1988-09-14	Dérivés du 1-carbonyl-1-phényl-2-azolyl-éthanol possédant des propriétés microbicides et étant des agents régulateurs de croissance des plantes et leurs intermédiaires
DE3801233A1 (de)	1988-08-04	Mikrobizides mittel
EP0086173B1 (fr)	1986-09-03	Dérivés de triazolcarbinols possédant une activité fongicide et étant des agents de régulation de croissance des plantes
EP0149426B1 (fr)	1988-05-04	Microbicides
EP0082340B1 (fr)	1990-01-03	Triazolyl-éthyl-éthers
EP0112292B1 (fr)	1987-07-29	Régulateurs de croissance des végétaux et microbicides
EP0163606B1 (fr)	1989-09-06	Dérivés de 1-fluoro-1-azolyl-2,2-diaryléthane à activité microbicide
EP0070798A2 (fr)	1983-01-26	Microbicides et régulateurs de croissance
EP0091398A1 (fr)	1983-10-12	Dérivés de l'azolylpropane à action microbicide et régulatrice de croissance des plantes
DE2943631A1 (de)	1980-05-14	Azolylketale, verfahren zu ihrer herstellung und ihre verwendung als mikrobizide
EP0079856A1 (fr)	1983-05-25	Microbicide triazolyl-vinyl éthers
EP0116262B1 (fr)	1989-12-27	Dérivés du fluor azolyl propanol, microbicides et agents régulateurs de croissance des plantes
EP0228343A2 (fr)	1987-07-08	Dérivés microbiens de 2-(1-triazolyl)-1-phényl-éthanone-(1)-cétals
EP0296518A1 (fr)	1988-12-28	Dérivés de phényléthers comme microbicide, procédé de leur préparation et leur application
EP0060962B1 (fr)	1985-08-07	Triazolylméthyldioxolanes microbicides et leur préparation
EP0228995A1 (fr)	1987-07-15	Microbicides
EP0113644A2 (fr)	1984-07-18	Dérivés d'halogénoazolyl propane, microbicides et agents régulateurs de croissance des plantes
NZ208208A (en)	1987-06-30	Pyridine derivatives and microbicidal compositions
EP0443980A1 (fr)	1991-08-28	Microbicides
DE3224186A1 (de)	1983-01-20	Mikrobizide und wuchsregulierende mittel
EP0215307B1 (fr)	1991-07-24	Dérivés de la pyrimidine, leur procédé de préparation et leur application en tant que microbicides