DD228442A5 - Insektizide, akarizide, nematizide mittel - Google Patents

Insektizide, akarizide, nematizide mittel Download PDF

Info

Publication number: DD228442A5
Authority: DD; German Democratic Republic
Prior art keywords: alkyl; formula; compounds; active ingredient; insecticides
Prior art date: 1983-11-18

Application number

DD84269571A

Other languages

German (de)

English (en)

Inventor

Gerhard Salbeck

Guenter Kratt

Gerhard Burghardt

Werner Knauf

Anna Waltersdorfer

Original Assignee

Hoechst Ag

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.)

1983-11-18

Filing date

1984-11-16

Publication date

1985-10-16

1984-11-16 Application filed by Hoechst Ag filed Critical Hoechst Ag

1985-10-16 Publication of DD228442A5 publication Critical patent/DD228442A5/de

Links

239000005645 nematicide Substances 0.000 title claims description 8
239000002917 insecticide Substances 0.000 title description 8
239000000642 acaricide Substances 0.000 title description 6
150000001875 compounds Chemical class 0.000 claims abstract description 27
230000000895 acaricidal effect Effects 0.000 claims abstract description 12
230000000749 insecticidal effect Effects 0.000 claims abstract description 6
125000000217 alkyl group Chemical group 0.000 abstract description 8
229910052736 halogen Inorganic materials 0.000 abstract description 8
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 8
125000004414 alkyl thio group Chemical group 0.000 abstract description 3
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract description 3
125000003545 alkoxy group Chemical group 0.000 abstract 2
125000004663 dialkyl amino group Chemical group 0.000 abstract 2
125000005843 halogen group Chemical group 0.000 abstract 1
239000004480 active ingredient Substances 0.000 description 20
-1 alkyl radical Chemical class 0.000 description 8
239000008187 granular material Substances 0.000 description 8
238000000034 method Methods 0.000 description 8
239000002253 acid Substances 0.000 description 7
150000002367 halogens Chemical class 0.000 description 7
239000000203 mixture Substances 0.000 description 7
CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
238000002360 preparation method Methods 0.000 description 6
239000011734 sodium Substances 0.000 description 6
239000000243 solution Substances 0.000 description 6
239000002904 solvent Substances 0.000 description 6
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 5
239000004495 emulsifiable concentrate Substances 0.000 description 5
229910052708 sodium Inorganic materials 0.000 description 5
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
241000239290 Araneae Species 0.000 description 4
241000196324 Embryophyta Species 0.000 description 4
241000244206 Nematoda Species 0.000 description 4
244000046052 Phaseolus vulgaris Species 0.000 description 4
VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
239000012141 concentrate Substances 0.000 description 4
JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 4
229940042400 direct acting antivirals phosphonic acid derivative Drugs 0.000 description 4
239000003995 emulsifying agent Substances 0.000 description 4
230000001069 nematicidal effect Effects 0.000 description 4
150000003007 phosphonic acid derivatives Chemical class 0.000 description 4
239000000843 powder Substances 0.000 description 4
239000002689 soil Substances 0.000 description 4
150000003579 thiophosphoric acid derivatives Chemical class 0.000 description 4
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
241000462639 Epilachna varivestis Species 0.000 description 3
LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 3
XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 3
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OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
235000010627 Phaseolus vulgaris Nutrition 0.000 description 3
ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 3
239000013543 active substance Substances 0.000 description 3
239000011230 binding agent Substances 0.000 description 3
150000001768 cations Chemical group 0.000 description 3
235000014113 dietary fatty acids Nutrition 0.000 description 3
239000000839 emulsion Substances 0.000 description 3
150000002170 ethers Chemical class 0.000 description 3
239000000194 fatty acid Substances 0.000 description 3
229930195729 fatty acid Natural products 0.000 description 3
150000002191 fatty alcohols Chemical class 0.000 description 3
238000009472 formulation Methods 0.000 description 3
229910052739 hydrogen Inorganic materials 0.000 description 3
239000001257 hydrogen Substances 0.000 description 3
239000000463 material Substances 0.000 description 3
229910052760 oxygen Inorganic materials 0.000 description 3
239000000126 substance Substances 0.000 description 3
125000006526 (C1-C2) alkyl group Chemical group 0.000 description 2
GXJQMKFJQFGQKV-KHPPLWFESA-N 2-[methyl-[(z)-octadec-9-enoyl]amino]ethanesulfonic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)N(C)CCS(O)(=O)=O GXJQMKFJQFGQKV-KHPPLWFESA-N 0.000 description 2
VONWPEXRCLHKRJ-UHFFFAOYSA-N 2-chloro-n-phenylacetamide Chemical class ClCC(=O)NC1=CC=CC=C1 VONWPEXRCLHKRJ-UHFFFAOYSA-N 0.000 description 2
241000489242 Amphitetranychus viennensis Species 0.000 description 2
241001124076 Aphididae Species 0.000 description 2
241001425390 Aphis fabae Species 0.000 description 2
241001600408 Aphis gossypii Species 0.000 description 2
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HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
241000254173 Coleoptera Species 0.000 description 2
229920000742 Cotton Polymers 0.000 description 2
241001635274 Cydia pomonella Species 0.000 description 2
XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 2
241000258937 Hemiptera Species 0.000 description 2
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
241000258916 Leptinotarsa decemlineata Species 0.000 description 2
244000141359 Malus pumila Species 0.000 description 2
LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
241000488583 Panonychus ulmi Species 0.000 description 2
GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
239000000654 additive Substances 0.000 description 2
150000003863 ammonium salts Chemical class 0.000 description 2
239000000969 carrier Substances 0.000 description 2
239000000460 chlorine Substances 0.000 description 2
239000007859 condensation product Substances 0.000 description 2
238000010790 dilution Methods 0.000 description 2
239000012895 dilution Substances 0.000 description 2
239000002270 dispersing agent Substances 0.000 description 2
230000000694 effects Effects 0.000 description 2
150000002148 esters Chemical class 0.000 description 2
239000003337 fertilizer Substances 0.000 description 2
239000000417 fungicide Substances 0.000 description 2
239000004009 herbicide Substances 0.000 description 2
150000002431 hydrogen Chemical group 0.000 description 2
150000003018 phosphorus compounds Chemical class 0.000 description 2
229920000151 polyglycol Polymers 0.000 description 2
239000010695 polyglycol Substances 0.000 description 2
239000000376 reactant Substances 0.000 description 2
239000007787 solid Substances 0.000 description 2
241000894007 species Species 0.000 description 2
239000007921 spray Substances 0.000 description 2
229910052717 sulfur Inorganic materials 0.000 description 2
239000000454 talc Substances 0.000 description 2
229910052623 talc Inorganic materials 0.000 description 2
VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 2
239000000080 wetting agent Substances 0.000 description 2
125000006536 (C1-C2)alkoxy group Chemical group 0.000 description 1
125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
FOGYNLXERPKEGN-UHFFFAOYSA-N 3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfopropyl)phenoxy]propane-1-sulfonic acid Chemical compound COC1=CC=CC(CC(CS(O)(=O)=O)OC=2C(=CC(CCCS(O)(=O)=O)=CC=2)OC)=C1O FOGYNLXERPKEGN-UHFFFAOYSA-N 0.000 description 1
241000238876 Acari Species 0.000 description 1
239000005995 Aluminium silicate Substances 0.000 description 1
241001480736 Amblyomma hebraeum Species 0.000 description 1
244000144730 Amygdalus persica Species 0.000 description 1
241000254175 Anthonomus grandis Species 0.000 description 1
241000294569 Aphelenchoides Species 0.000 description 1
241000952611 Aphis craccivora Species 0.000 description 1
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
241001350371 Capua Species 0.000 description 1
241001107116 Castanospermum australe Species 0.000 description 1
241001121020 Cetonia aurata Species 0.000 description 1
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
241000207199 Citrus Species 0.000 description 1
241000399934 Ditylenchus Species 0.000 description 1
241000353522 Earias insulana Species 0.000 description 1
241001301805 Epilachna Species 0.000 description 1
241000738498 Epitrix pubescens Species 0.000 description 1
244000307700 Fragaria vesca Species 0.000 description 1
235000016623 Fragaria vesca Nutrition 0.000 description 1
235000011363 Fragaria x ananassa Nutrition 0.000 description 1
208000001034 Frostbite Diseases 0.000 description 1
241001442498 Globodera Species 0.000 description 1
241001147381 Helicoverpa armigera Species 0.000 description 1
241000255967 Helicoverpa zea Species 0.000 description 1
241001480224 Heterodera Species 0.000 description 1
241001480807 Hyalomma marginatum Species 0.000 description 1
239000005909 Kieselgur Substances 0.000 description 1
241000255777 Lepidoptera Species 0.000 description 1
229920001732 Lignosulfonate Polymers 0.000 description 1
241001220360 Longidorus Species 0.000 description 1
235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
241001300479 Macroptilium Species 0.000 description 1
235000017679 Malus communis Nutrition 0.000 description 1
235000011430 Malus pumila Nutrition 0.000 description 1
235000015103 Malus silvestris Nutrition 0.000 description 1
241001143352 Meloidogyne Species 0.000 description 1
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241001465754 Metazoa Species 0.000 description 1
241000721621 Myzus persicae Species 0.000 description 1
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
241000258913 Oncopeltus fasciatus Species 0.000 description 1
241000346285 Ostrinia furnacalis Species 0.000 description 1
241001147398 Ostrinia nubilalis Species 0.000 description 1
241000488581 Panonychus citri Species 0.000 description 1
241000275067 Phyllotreta Species 0.000 description 1
239000004372 Polyvinyl alcohol Substances 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
241000193943 Pratylenchus Species 0.000 description 1
235000006040 Prunus persica var persica Nutrition 0.000 description 1
239000006004 Quartz sand Substances 0.000 description 1
241000201377 Radopholus Species 0.000 description 1
241000238680 Rhipicephalus microplus Species 0.000 description 1
PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 1
229920002125 Sokalan® Polymers 0.000 description 1
240000003768 Solanum lycopersicum Species 0.000 description 1
241001454295 Tetranychidae Species 0.000 description 1
241001454294 Tetranychus Species 0.000 description 1
241001454293 Tetranychus urticae Species 0.000 description 1
241001238451 Tortrix viridana Species 0.000 description 1
241000976088 Tropinota hirta Species 0.000 description 1
240000006677 Vicia faba Species 0.000 description 1
235000010749 Vicia faba Nutrition 0.000 description 1
241000201423 Xiphinema Species 0.000 description 1
241000607479 Yersinia pestis Species 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
229910052783 alkali metal Inorganic materials 0.000 description 1
150000008044 alkali metal hydroxides Chemical class 0.000 description 1
125000002877 alkyl aryl group Chemical group 0.000 description 1
125000005037 alkyl phenyl group Chemical group 0.000 description 1
235000012211 aluminium silicate Nutrition 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
150000003931 anilides Chemical class 0.000 description 1
239000007900 aqueous suspension Substances 0.000 description 1
229960000892 attapulgite Drugs 0.000 description 1
239000002585 base 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
235000021279 black bean Nutrition 0.000 description 1
238000009835 boiling Methods 0.000 description 1
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
229910052794 bromium Inorganic materials 0.000 description 1
159000000007 calcium salts Chemical class 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
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000012876 carrier material Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
238000007796 conventional method Methods 0.000 description 1
230000006378 damage Effects 0.000 description 1
239000003085 diluting agent Substances 0.000 description 1
239000003814 drug Substances 0.000 description 1
229940079593 drug Drugs 0.000 description 1
238000001035 drying Methods 0.000 description 1
239000000428 dust Substances 0.000 description 1
235000013399 edible fruits Nutrition 0.000 description 1
150000004665 fatty acids Chemical class 0.000 description 1
239000000945 filler Substances 0.000 description 1
239000000706 filtrate Substances 0.000 description 1
238000000227 grinding Methods 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
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 1
239000007788 liquid Substances 0.000 description 1
238000004519 manufacturing process Methods 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
VUZPPFZMUPKLLV-UHFFFAOYSA-N methane;hydrate Chemical compound C.O VUZPPFZMUPKLLV-UHFFFAOYSA-N 0.000 description 1
238000003801 milling Methods 0.000 description 1
239000002480 mineral oil Substances 0.000 description 1
LWGJTAZLEJHCPA-UHFFFAOYSA-N n-(2-chloroethyl)-n-nitrosomorpholine-4-carboxamide Chemical compound ClCCN(N=O)C(=O)N1CCOCC1 LWGJTAZLEJHCPA-UHFFFAOYSA-N 0.000 description 1
150000002825 nitriles Chemical class 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
229920000847 nonoxynol Polymers 0.000 description 1
SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
230000001473 noxious effect Effects 0.000 description 1
239000003921 oil Substances 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
150000003014 phosphoric acid esters Chemical class 0.000 description 1
229910052698 phosphorus Inorganic materials 0.000 description 1
239000011574 phosphorus Substances 0.000 description 1
239000004584 polyacrylic acid Substances 0.000 description 1
229920000570 polyether Polymers 0.000 description 1
229920001522 polyglycol ester Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000011591 potassium Substances 0.000 description 1
229910052700 potassium Inorganic materials 0.000 description 1
239000000047 product Substances 0.000 description 1
239000011814 protection agent Substances 0.000 description 1
239000008262 pumice Substances 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
239000010453 quartz Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
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235000011152 sodium sulphate Nutrition 0.000 description 1
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239000000725 suspension Substances 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
238000001665 trituration Methods 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
239000008096 xylene Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- C07F9/165—Esters of thiophosphoric acids
- C07F9/1651—Esters of thiophosphoric acids with hydroxyalkyl compounds with further substituents on alkyl
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/16—Esters of thiophosphoric acids or thiophosphorous acids
- 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34
- A01N57/06—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having alternatively specified atoms bound to the phosphorus atom and not covered by a single one of groups A01N57/10, A01N57/18, A01N57/26, A01N57/34 containing aromatic radicals
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/06—Phosphorus compounds without P—C bonds
- C07F9/22—Amides of acids of phosphorus
- C07F9/24—Esteramides
- C07F9/2404—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/2408—Esteramides the ester moiety containing a substituent or a structure which is considered as characteristic of hydroxyalkyl compounds
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/38—Phosphonic acids [RP(=O)(OH)2]; Thiophosphonic acids ; [RP(=X1)(X2H)2(X1, X2 are each independently O, S or Se)]
- C07F9/40—Esters thereof
- C07F9/4071—Esters thereof the ester moiety containing a substituent or a structure which is considered as characteristic
- C07F9/4075—Esters with hydroxyalkyl compounds

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Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Health & Medical Sciences (AREA)
General Health & Medical Sciences (AREA)
Biochemistry (AREA)
Molecular Biology (AREA)
Pest Control & Pesticides (AREA)
Agronomy & Crop Science (AREA)
Plant Pathology (AREA)
Engineering & Computer Science (AREA)
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DD84269571A 1983-11-18 1984-11-16 Insektizide, akarizide, nematizide mittel DD228442A5 (de)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19833341669 DE3341669A1 (de)	1983-11-18	1983-11-18	Neue (di)thiophosphor- und phosphonsaeure-derivate und ihre verwendung im pflanzenschutz

Publications (1)

Publication Number	Publication Date
DD228442A5 true DD228442A5 (de)	1985-10-16

Family

ID=6214616

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD84269571A DD228442A5 (de)	1983-11-18	1984-11-16	Insektizide, akarizide, nematizide mittel

Country Status (15)

Country	Link
EP (1)	EP0142782A3 (fr)
JP (1)	JPS60116694A (fr)
KR (1)	KR850004110A (fr)
AU (1)	AU3563384A (fr)
BR (1)	BR8405847A (fr)
DD (1)	DD228442A5 (fr)
DE (1)	DE3341669A1 (fr)
DK (1)	DK547884A (fr)
ES (1)	ES537671A0 (fr)
GR (1)	GR80953B (fr)
HU (1)	HUT37003A (fr)
IL (1)	IL73526A0 (fr)
MA (1)	MA20268A1 (fr)
OA (1)	OA07867A (fr)
ZA (1)	ZA848941B (fr)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US5199976A (en) *	1991-06-13	1993-04-06	The Gillette Company	Ozone-friendly correction fluid

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
NL7700930A (nl) *	1976-02-04	1977-08-08	Hoechst Ag	Plantenbeschermingsmiddel.
DE2604224A1 (de) *	1976-02-04	1977-08-11	Hoechst Ag	Herbizide mittel
GB2004187B (en) *	1977-09-14	1982-05-26	Ici Australia Ltd	Insecticides

1983
- 1983-11-18 DE DE19833341669 patent/DE3341669A1/de not_active Withdrawn
1984
- 1984-11-08 EP EP84113480A patent/EP0142782A3/fr not_active Withdrawn
- 1984-11-12 HU HU844206A patent/HUT37003A/hu unknown
- 1984-11-15 ES ES537671A patent/ES537671A0/es active Granted
- 1984-11-16 AU AU35633/84A patent/AU3563384A/en not_active Abandoned
- 1984-11-16 BR BR8405847A patent/BR8405847A/pt unknown
- 1984-11-16 OA OA58444A patent/OA07867A/fr unknown
- 1984-11-16 IL IL73526A patent/IL73526A0/xx unknown
- 1984-11-16 JP JP59240871A patent/JPS60116694A/ja active Pending
- 1984-11-16 DD DD84269571A patent/DD228442A5/de unknown
- 1984-11-16 ZA ZA848941A patent/ZA848941B/xx unknown
- 1984-11-16 GR GR80953A patent/GR80953B/el unknown
- 1984-11-16 KR KR1019840007191A patent/KR850004110A/ko not_active Withdrawn
- 1984-11-16 DK DK547884A patent/DK547884A/da not_active Application Discontinuation
- 1984-11-16 MA MA20492A patent/MA20268A1/fr unknown

Also Published As

Publication number	Publication date
ZA848941B (en)	1985-07-31
AU3563384A (en)	1985-05-23
GR80953B (en)	1985-03-15
ES8507564A1 (es)	1985-09-16
BR8405847A (pt)	1985-09-17
ES537671A0 (es)	1985-09-16
MA20268A1 (fr)	1985-07-01
JPS60116694A (ja)	1985-06-24
OA07867A (fr)	1986-11-20
IL73526A0 (en)	1985-02-28
DE3341669A1 (de)	1985-05-30
EP0142782A2 (fr)	1985-05-29
EP0142782A3 (fr)	1985-07-03
KR850004110A (ko)	1985-07-01
HUT37003A (en)	1985-11-28
DK547884D0 (da)	1984-11-16
DK547884A (da)	1985-05-19

Publication	Publication Date	Title
DE1238902B (de)	1967-04-20	Verfahren zur Herstellung von Phosphor-, Phosphon- bzw. Thionophosphor-, -phosphon-saeureestern
DE2617736C2 (de)	1982-12-09	Schädlingsbekämpfungsmittel
EP0100528A2 (fr)	1984-02-15	Dérivés d'acides (di)-thiophosphoriques et (di)-thiophosphoniques, leur procédé de préparation, composition les contenant et son utilisation pour la protection des plantes
US4024277A (en)	1977-05-17	Phosphoro-aminosulfenyl derivatives of benzofuran carbamates
DE2732930C2 (de)	1985-08-14	Neue 0-Äthyl-S-n-propyl-O-2,2,2- trihalogenäthylphosphorthiolate (oder -thionothiolate), Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und Nematizide
DD144860A5 (de)	1980-11-12	Schaedlingsbekaempfungsmittel
CH631721A5 (de)	1982-08-31	Pflanzenschutzmittel.
DE3118257A1 (de)	1982-12-02	Pestizide s(-1.2.4-triazol-5-ylmethyl)-(di)-thiophosph(on)ate und verfahren zu ihrer herstellung
DE2629016C2 (de)	1983-11-10	O-(1-Fluor-2-halogen-äthyl)(thiono) phosphor(phosphon)-säureesteramide, Verfahren zu ihrer Herstellung und ihre Verwendung als Insektizide, Akarizide und Nematizide
DD228442A5 (de)	1985-10-16	Insektizide, akarizide, nematizide mittel
DE2630561A1 (de)	1978-01-19	1-fluor-2-halogen-aethyl-thionophosphor (phosphon)-saeureester, verfahren zu ihrer herstellung und ihre verwendung als insektizide, akarizide und nematizide
DE3510178A1 (de)	1986-09-25	Neue halogenalkylthiosubstituierte heterocyclen, verfahren zu ihrer herstellung und ihre verwendung im pflanzenschutz
CS199738B2 (en)	1980-07-31	Insecticide,acaricide and nematocide and process for preparing effective compounds
DE2741086A1 (de)	1978-03-23	Neue phosphorsaeureesteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide und akarizide
EP0011802A1 (fr)	1980-06-11	Amides d'acides phénoxy-phénoxy-propioniques, procédés pour leur préparation, compositions herbicides les contenant et leur application à la lutte contre les mauvaises herbes
DE2709617A1 (de)	1978-09-07	O-(1-fluor-2-halogen-aethyl)(thiono) phosphor(phosphon)-saeureesteramide, verfahren zu ihrer herstellung und ihre verwendung als insektizide, akarizide und nematizide
DE2451911A1 (de)	1975-05-07	Phosphorylformamidine, verfahren zu ihrer herstellung und ihre verwendung in der schaedlingsbekaempfung
AT367768B (de)	1982-07-26	Verfahren zur herstellung von neuen organischen phosphorsaeureestern
DE2422324C2 (de)	1984-05-03	Diphenyläther-phosphorverbindungen, Verfahren zu ihrer Herstellung und diese enthaltende Schädlingsbekämpfungsmittel
EP0035971A2 (fr)	1981-09-16	Oxime phosphates, procédé pour leur préparation et leur utilisation comme pesticides
AT258959B (de)	1967-12-27	Verfahren zur Herstellung von neuen Phosphorsäureestern
DE1568639A1 (de)	1970-03-26	Verfahren zur Herstellung von 2,2-Dichlor-vinylphosphorsaeureesteramiden
KR820000078B1 (ko)	1982-02-10	N-치환된 페닐 카바모일 메틸 티오포스포네이트유도체의 제조방법
DE2360493A1 (de)	1975-06-12	Bernsteinsaeureoximidphosphorsaeureester
DE2418363A1 (de)	1974-10-24	1,2,4-thiadiazolyl-phosphorverbindungen, verfahren zu ihrer herstellung und ihre verwendung