DD152901A5 - Azolylketale als mikrobizide - Google Patents

Azolylketale als mikrobizide Download PDF

Info

Publication number: DD152901A5
Authority: DD; German Democratic Republic
Prior art keywords: butyl; tert; item; formula; methyl
Prior art date: 1978-11-01

Application number

DD79216587A

Other languages

German (de)

English (en)

Inventor

Elmar Sturm

Wolfgang Eckhardt

Bernhard Gloor

Robert Nyfeler

Original Assignee

Ciba Geigy 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.)

1978-11-01

Filing date

1979-10-31

Publication date

1981-12-16

1978-11-01 Priority claimed from CH1124778A external-priority patent/CH639658A5/de

1978-11-01 Priority claimed from CH1124678A external-priority patent/CH639657A5/de

1979-10-31 Application filed by Ciba Geigy Ag filed Critical Ciba Geigy Ag

1981-12-16 Publication of DD152901A5 publication Critical patent/DD152901A5/de

Links

229940124561 microbicide Drugs 0.000 title description 4
150000001875 compounds Chemical class 0.000 claims abstract description 32
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 7
244000005700 microbiome Species 0.000 claims abstract description 4
230000003449 preventive effect Effects 0.000 claims abstract description 3
239000000575 pesticide Substances 0.000 claims abstract 2
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 36
-1 C 1 -C 6 -alkyl Chemical group 0.000 claims description 30
239000000203 mixture Substances 0.000 claims description 26
101000588924 Anthopleura elegantissima Delta-actitoxin-Ael1a Proteins 0.000 claims description 19
125000001309 chloro group Chemical group Cl* 0.000 claims description 18
239000000460 chlorine Substances 0.000 claims description 13
229910052801 chlorine Inorganic materials 0.000 claims description 12
125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 10
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 10
229910052739 hydrogen Inorganic materials 0.000 claims description 10
239000001257 hydrogen Substances 0.000 claims description 10
ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims description 7
206010061217 Infestation Diseases 0.000 claims description 6
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 6
239000004305 biphenyl Substances 0.000 claims description 6
235000010290 biphenyl Nutrition 0.000 claims description 6
125000004093 cyano group Chemical group *C#N 0.000 claims description 6
125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 claims description 5
WNXJIVFYUVYPPR-UHFFFAOYSA-N 1,3-dioxolane Chemical compound C1COCO1 WNXJIVFYUVYPPR-UHFFFAOYSA-N 0.000 claims description 5
125000006267 biphenyl group Chemical group 0.000 claims description 5
229910052751 metal Chemical class 0.000 claims description 5
239000002184 metal Chemical class 0.000 claims description 5
HRDXJKGNWSUIBT-UHFFFAOYSA-N methoxybenzene Chemical group [CH2]OC1=CC=CC=C1 HRDXJKGNWSUIBT-UHFFFAOYSA-N 0.000 claims description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
239000005977 Ethylene Substances 0.000 claims description 4
125000000217 alkyl group Chemical group 0.000 claims description 4
239000000969 carrier Substances 0.000 claims description 4
229910052736 halogen Inorganic materials 0.000 claims description 4
125000005843 halogen group Chemical group 0.000 claims description 4
150000002431 hydrogen Chemical class 0.000 claims description 4
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 4
125000004849 alkoxymethyl group Chemical group 0.000 claims description 3
150000002367 halogens Chemical group 0.000 claims description 3
150000003839 salts Chemical class 0.000 claims description 3
125000000383 tetramethylene group Chemical group [H]C([H])([*:1])C([H])([H])C([H])([H])C([H])([H])[*:2] 0.000 claims description 3
QDKWLJJOYIFEBS-UHFFFAOYSA-N 1-fluoro-4-$l^{1}-oxidanylbenzene Chemical group [O]C1=CC=C(F)C=C1 QDKWLJJOYIFEBS-UHFFFAOYSA-N 0.000 claims description 2
HTWIZMNMTWYQRN-UHFFFAOYSA-N 2-methyl-1,3-dioxolane Chemical compound CC1OCCO1 HTWIZMNMTWYQRN-UHFFFAOYSA-N 0.000 claims description 2
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239000011737 fluorine Substances 0.000 claims description 2
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125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 3
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239000013078 crystal Substances 0.000 description 8
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239000000654 additive Substances 0.000 description 6
239000008187 granular material Substances 0.000 description 6
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238000006243 chemical reaction Methods 0.000 description 5
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239000000126 substance Substances 0.000 description 5
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241000221300 Puccinia Species 0.000 description 1
241000221535 Pucciniales Species 0.000 description 1
241000220324 Pyrus Species 0.000 description 1
235000004443 Ricinus communis Nutrition 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
241000209056 Secale Species 0.000 description 1
235000007238 Secale cereale Nutrition 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
235000009470 Theobroma cacao Nutrition 0.000 description 1
244000299461 Theobroma cacao Species 0.000 description 1
241000722133 Tilletia Species 0.000 description 1
241000736772 Uria Species 0.000 description 1
240000001717 Vaccinium macrocarpon Species 0.000 description 1
244000078534 Vaccinium myrtillus Species 0.000 description 1
241000317942 Venturia <ichneumonid wasp> Species 0.000 description 1
241000082085 Verticillium <Phyllachorales> Species 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
HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
239000002250 absorbent Substances 0.000 description 1
230000002745 absorbent Effects 0.000 description 1
230000000996 additive effect Effects 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
239000000443 aerosol Substances 0.000 description 1
239000003513 alkali Substances 0.000 description 1
229910052783 alkali metal Inorganic materials 0.000 description 1
150000001340 alkali metals Chemical class 0.000 description 1
150000001342 alkaline earth metals Chemical class 0.000 description 1
150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
125000002947 alkylene group Chemical group 0.000 description 1
235000020224 almond Nutrition 0.000 description 1
PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
229910000147 aluminium phosphate Inorganic materials 0.000 description 1
150000001412 amines Chemical class 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
235000019400 benzoyl peroxide Nutrition 0.000 description 1
235000021028 berry Nutrition 0.000 description 1
239000011230 binding agent Substances 0.000 description 1
QKSKPIVNLNLAAV-UHFFFAOYSA-N bis(2-chloroethyl) sulfide Chemical compound ClCCSCCCl QKSKPIVNLNLAAV-UHFFFAOYSA-N 0.000 description 1
235000021029 blackberry Nutrition 0.000 description 1
229920005551 calcium lignosulfonate Polymers 0.000 description 1
RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
235000009120 camo Nutrition 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
125000004432 carbon atom Chemical group C* 0.000 description 1
BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
150000004649 carbonic acid derivatives Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
150000001768 cations Chemical class 0.000 description 1
235000005607 chanvre indien Nutrition 0.000 description 1
235000019693 cherries Nutrition 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
239000011248 coating agent Substances 0.000 description 1
238000000576 coating method Methods 0.000 description 1
235000016213 coffee Nutrition 0.000 description 1
235000013353 coffee beverage Nutrition 0.000 description 1
238000001816 cooling Methods 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
235000005822 corn Nutrition 0.000 description 1
235000021019 cranberries Nutrition 0.000 description 1
244000038559 crop plants Species 0.000 description 1
238000005520 cutting process Methods 0.000 description 1
239000012973 diazabicyclooctane Substances 0.000 description 1
238000010790 dilution Methods 0.000 description 1
239000012895 dilution Substances 0.000 description 1
150000002009 diols Chemical class 0.000 description 1
239000002270 dispersing agent Substances 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
239000000284 extract Substances 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000000835 fiber Substances 0.000 description 1
239000012467 final product Substances 0.000 description 1
125000001153 fluoro group Chemical group F* 0.000 description 1
239000000446 fuel Substances 0.000 description 1
229910021485 fumed silica Inorganic materials 0.000 description 1
230000002538 fungal effect Effects 0.000 description 1
150000004820 halides Chemical class 0.000 description 1
230000002140 halogenating effect Effects 0.000 description 1
230000026030 halogenation Effects 0.000 description 1
238000005658 halogenation reaction Methods 0.000 description 1
239000011487 hemp Substances 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
150000004678 hydrides Chemical class 0.000 description 1
229930195733 hydrocarbon Natural products 0.000 description 1
150000002430 hydrocarbons Chemical class 0.000 description 1
XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
150000004679 hydroxides Chemical class 0.000 description 1
235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
239000012442 inert solvent Substances 0.000 description 1
150000007529 inorganic bases Chemical class 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000000543 intermediate Substances 0.000 description 1
239000013067 intermediate product Substances 0.000 description 1
239000011630 iodine Substances 0.000 description 1
229910052740 iodine Inorganic materials 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000005907 ketalization reaction Methods 0.000 description 1
235000021374 legumes Nutrition 0.000 description 1
239000000463 material Substances 0.000 description 1
235000019988 mead Nutrition 0.000 description 1
150000002739 metals Chemical class 0.000 description 1
229940098779 methanesulfonic acid Drugs 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
239000011707 mineral Substances 0.000 description 1
235000010755 mineral Nutrition 0.000 description 1
235000010460 mustard Nutrition 0.000 description 1
150000002823 nitrates Chemical class 0.000 description 1
229910017604 nitric acid Inorganic materials 0.000 description 1
235000014571 nuts Nutrition 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
235000006408 oxalic acid Nutrition 0.000 description 1
229940116315 oxalic acid Drugs 0.000 description 1
235000021017 pears Nutrition 0.000 description 1
239000008188 pellet Substances 0.000 description 1
125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
150000002978 peroxides Chemical class 0.000 description 1
230000000361 pesticidal effect Effects 0.000 description 1
239000012071 phase Substances 0.000 description 1
235000021317 phosphate Nutrition 0.000 description 1
150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
235000015047 pilsener Nutrition 0.000 description 1
PJGSXYOJTGTZAV-UHFFFAOYSA-N pinacolone Chemical compound CC(=O)C(C)(C)C PJGSXYOJTGTZAV-UHFFFAOYSA-N 0.000 description 1
235000021018 plums Nutrition 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920001223 polyethylene glycol Polymers 0.000 description 1
VBCFDVLVYCYDFZ-UHFFFAOYSA-N potassium;1h-1,2,4-triazole Chemical compound [K].C=1N=CNN=1 VBCFDVLVYCYDFZ-UHFFFAOYSA-N 0.000 description 1
235000012015 potatoes Nutrition 0.000 description 1
239000000047 product Substances 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
235000015136 pumpkin Nutrition 0.000 description 1
238000000746 purification Methods 0.000 description 1
UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
238000001953 recrystallisation Methods 0.000 description 1
238000010992 reflux Methods 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide Nutrition 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000004575 stone Substances 0.000 description 1
125000001424 substituent group Chemical group 0.000 description 1
HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical class O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
150000003892 tartrate salts Chemical class 0.000 description 1
235000013616 tea Nutrition 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
229960004319 trichloroacetic acid Drugs 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
239000008096 xylene Substances 0.000 description 1
239000011701 zinc Substances 0.000 description 1
229910052725 zinc Inorganic materials 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- 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
- 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
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
- C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
- C07D317/10—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings
- C07D317/14—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 not condensed with other rings with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D317/18—Radicals substituted by singly bound oxygen or sulfur atoms
- C07D317/22—Radicals substituted by singly bound oxygen or sulfur atoms etherified

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Plant Pathology (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Agricultural Chemicals And Associated Chemicals (AREA)
Plural Heterocyclic Compounds (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DD79216587A 1978-11-01 1979-10-31 Azolylketale als mikrobizide DD152901A5 (de)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
CH1124778A CH639658A5 (en)	1978-11-01	1978-11-01	Dioxane and dioxolane derivatives having a microbicidal action
CH1124678A CH639657A5 (en)	1978-11-01	1978-11-01	Dioxane and dioxolane derivatives having a microbicidal action

Publications (1)

Publication Number	Publication Date
DD152901A5 true DD152901A5 (de)	1981-12-16

Family

ID=25708031

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DD79216587A DD152901A5 (de)	1978-11-01	1979-10-31	Azolylketale als mikrobizide

Country Status (19)

Country	Link
AT (1)	AT374339B (fr)
AU (1)	AU535098B2 (fr)
BR (1)	BR7907069A (fr)
CA (1)	CA1138465A (fr)
CS (1)	CS214809B2 (fr)
DD (1)	DD152901A5 (fr)
DE (1)	DE2943631A1 (fr)
DK (1)	DK461179A (fr)
ES (1)	ES8100802A1 (fr)
FR (1)	FR2440367A1 (fr)
GB (1)	GB2035315B (fr)
IL (1)	IL58583A0 (fr)
IT (1)	IT1124897B (fr)
NL (1)	NL7907953A (fr)
NZ (1)	NZ191989A (fr)
PL (1)	PL120450B1 (fr)
PT (1)	PT70388A (fr)
SE (1)	SE7909023L (fr)
TR (1)	TR20530A (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US4259505A (en) *	1980-03-04	1981-03-31	Ciba-Geigy Corporation	Process for the preparation of 1H-azole derivatives
DE3025879A1 (de) *	1980-07-09	1982-02-11	Basf Ag, 6700 Ludwigshafen	1,3-dioxan-5-yl-alkyltriazole, ihre herstellung, ihre verwendung zur regulierung des pflanzenwachstums und mittel dafuer
DE3026140A1 (de) *	1980-07-10	1982-02-18	Basf Ag, 6700 Ludwigshafen	1,3-dioxan-5-yl-alkenyltriazole, ihre herstellung, ihre verwendung zur regulierung des pflanzenwachstums und mittel dafuer
DE3171736D1 (en) *	1980-12-10	1985-09-12	Ciba Geigy Ag	Microbicidal triazolyl methyl dioxolanes and their preparation
DE3104311A1 (de) *	1981-02-07	1982-08-19	Bayer Ag, 5090 Leverkusen	2-azolylmethyl-1,3-dioxolan- und -dioxan-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide
DE3104380A1 (de) *	1981-02-07	1982-08-19	Bayer Ag, 5090 Leverkusen	Antimikrobielle mittel
DE3374123D1 (en) *	1982-04-01	1987-11-26	Schering Agrochemicals Ltd	Heterocyclic fungicidal and growth regulant compounds, and compositions containing them
DE3231334A1 (de) *	1982-08-24	1984-03-01	Basf Ag, 6700 Ludwigshafen	Dioxanylazolderivate, diese enthaltende fungizide mittel und verfahren zur bekaempfung von pilzen mit diesen verbindungen
EP2746278A1 (fr)	2012-12-19	2014-06-25	Basf Se	Composés de [1,2,4]triazole et d'imidazole substitués

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
US3575999A (en) *	1968-08-19	1971-04-20	Janssen Pharmaceutica Nv	Ketal derivatives of imidazole
NZ179111A (en) *	1974-11-18	1978-03-06	Janssen Pharmaceutica Nv	I-(aryl)-ethyl-1h-1,2,4-triazole ketals,anti-microbial and plant growth controlling compositions

1979
- 1979-10-24 FR FR7926388A patent/FR2440367A1/fr active Granted
- 1979-10-26 TR TR20530A patent/TR20530A/xx unknown
- 1979-10-29 DE DE19792943631 patent/DE2943631A1/de not_active Ceased
- 1979-10-30 NL NL7907953A patent/NL7907953A/nl not_active Application Discontinuation
- 1979-10-30 CA CA000338788A patent/CA1138465A/fr not_active Expired
- 1979-10-30 IL IL58583A patent/IL58583A0/xx unknown
- 1979-10-30 PT PT70388A patent/PT70388A/pt unknown
- 1979-10-30 CS CS797379A patent/CS214809B2/cs unknown
- 1979-10-31 NZ NZ191989A patent/NZ191989A/xx unknown
- 1979-10-31 BR BR7907069A patent/BR7907069A/pt unknown
- 1979-10-31 GB GB7937797A patent/GB2035315B/en not_active Expired
- 1979-10-31 SE SE7909023A patent/SE7909023L/xx unknown
- 1979-10-31 DD DD79216587A patent/DD152901A5/de unknown
- 1979-10-31 PL PL1979219356A patent/PL120450B1/pl unknown
- 1979-10-31 AT AT0705179A patent/AT374339B/de not_active IP Right Cessation
- 1979-10-31 AU AU52347/79A patent/AU535098B2/en not_active Ceased
- 1979-10-31 DK DK461179A patent/DK461179A/da unknown
- 1979-10-31 ES ES485567A patent/ES8100802A1/es not_active Expired
- 1979-10-31 IT IT26996/79A patent/IT1124897B/it active

Also Published As

Publication number	Publication date
GB2035315A (en)	1980-06-18
BR7907069A (pt)	1980-09-02
IT1124897B (it)	1986-05-14
CS214809B2 (en)	1982-06-25
NZ191989A (en)	1982-03-16
GB2035315B (en)	1983-10-26
NL7907953A (nl)	1980-05-06
DE2943631A1 (de)	1980-05-14
SE7909023L (sv)	1980-05-02
TR20530A (tr)	1981-10-21
ES485567A0 (es)	1980-11-01
AU535098B2 (en)	1984-03-01
PL120450B1 (en)	1982-03-31
IT7926996A0 (it)	1979-10-31
AT374339B (de)	1984-04-10
FR2440367B1 (fr)	1983-03-18
CA1138465A (fr)	1982-12-28
FR2440367A1 (fr)	1980-05-30
DK461179A (da)	1980-05-02
PT70388A (en)	1979-11-01
PL219356A1 (fr)	1980-08-11
ES8100802A1 (es)	1980-11-01
AU5234779A (en)	1980-05-08
ATA705179A (de)	1983-09-15
IL58583A0 (en)	1980-01-31

Publication	Publication Date	Title
EP0065485B1 (fr)	1990-04-18	Dérivés d'arylphényléthers comme microbicide, procédé pour leur préparation et leur application
DD215930A5 (de)	1984-11-28	Mittel zur bekaempfung oder verhuetung eines befalls durch mikroorganismen
DD248274A5 (de)	1987-08-05	Mikrobizides mittel
EP0040345A1 (fr)	1981-11-25	Dérivés de 1-hydroxyéthyl-azoles, procédé pour leur préparation et leur utilisation comme fongicides et pour la régulation de la croissance des plantes
EP0114567A2 (fr)	1984-08-01	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
EP0291797A2 (fr)	1988-11-23	Dérivés d'hydroxyalkyl-triazoles
EP0029355B1 (fr)	1983-07-27	Azolylcétals, leur préparation et leur utilisation, et pesticides les contenant
EP0086173B1 (fr)	1986-09-03	Dérivés de triazolcarbinols possédant une activité fongicide et étant des agents de régulation de croissance des plantes
EP0060223A2 (fr)	1982-09-15	Agent microbicide
EP0004303B1 (fr)	1982-01-13	Dérivés acylés du 1-azolyl-2-hydroxy-butane, leur procédé de préparation ainsi que leur utilisation comme fongicides
CH648843A5 (de)	1985-04-15	1-(2-aryl-1,3-dioxolan-2-ylmethyl)-1h-1,2,4-triazole.
EP0025949A1 (fr)	1981-04-01	Triazolyl-gamma-fluoropinacolols acylés, procédé pour leur préparation et leur application comme fongicides
EP0082340B1 (fr)	1990-01-03	Triazolyl-éthyl-éthers
DD152901A5 (de)	1981-12-16	Azolylketale als mikrobizide
EP0112292B1 (fr)	1987-07-29	Régulateurs de croissance des végétaux et microbicides
EP0091398A1 (fr)	1983-10-12	Dérivés de l'azolylpropane à action microbicide et régulatrice de croissance des plantes
EP0070798A2 (fr)	1983-01-26	Microbicides et régulateurs de croissance
EP0044276A2 (fr)	1982-01-20	Dérivés de (1H-azolylméthyl)-4, dioxolan-1,3, one-5, leur préparation et leur emploi comme régulateurs de croissance des plantes et/ou pesticides
EP0079856A1 (fr)	1983-05-25	Microbicide triazolyl-vinyl éthers
EP0118069B1 (fr)	1986-12-30	Fongicides contenant des 1,3-diazolyl-propanols
EP0060962B1 (fr)	1985-08-07	Triazolylméthyldioxolanes microbicides et leur préparation
EP0116262B1 (fr)	1989-12-27	Dérivés du fluor azolyl propanol, microbicides et agents régulateurs de croissance des plantes
EP0102517B1 (fr)	1986-10-08	Agents fongicides
DD144353A5 (de)	1980-10-15	Fungizide mittel
EP0203440A2 (fr)	1986-12-03	Dérivés de dichlorocyclopropylalkyl-hydroxyalkyl-azoles