DE2634511A1 - Beta-azolylketone - Google Patents
Beta-azolylketoneInfo
- Publication number
- DE2634511A1 DE2634511A1 DE19762634511 DE2634511A DE2634511A1 DE 2634511 A1 DE2634511 A1 DE 2634511A1 DE 19762634511 DE19762634511 DE 19762634511 DE 2634511 A DE2634511 A DE 2634511A DE 2634511 A1 DE2634511 A1 DE 2634511A1
- Authority
- DE
- Germany
- Prior art keywords
- formula
- appropriate
- weight
- phenyl
- parts
- Prior art date
- Legal status (The legal status 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 status listed.)
- Withdrawn
Links
- 150000002576 ketones Chemical class 0.000 title claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 9
- 239000003085 diluting agent Substances 0.000 claims description 8
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 claims description 6
- 239000000417 fungicide Substances 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 241000233866 Fungi Species 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 5
- 239000003054 catalyst Substances 0.000 claims description 5
- 230000000855 fungicidal effect Effects 0.000 claims description 5
- 125000000217 alkyl group Chemical group 0.000 claims description 4
- 229910052736 halogen Inorganic materials 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 150000001299 aldehydes Chemical class 0.000 claims description 3
- 125000001624 naphthyl group Chemical group 0.000 claims description 3
- 125000001544 thienyl group Chemical group 0.000 claims description 3
- CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical compound [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 claims description 2
- 125000003302 alkenyloxy group Chemical group 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 239000011230 binding agent Substances 0.000 claims description 2
- 125000004432 carbon atom Chemical group C* 0.000 claims description 2
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 2
- 125000002541 furyl group Chemical group 0.000 claims description 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 2
- 125000003107 substituted aryl group Chemical group 0.000 claims description 2
- 230000003032 phytopathogenic effect Effects 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 description 25
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 15
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- 241000196324 Embryophyta Species 0.000 description 9
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- 206010061217 Infestation Diseases 0.000 description 9
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
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- -1 p-isopropyl-phenyl Chemical group 0.000 description 9
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
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- 239000006185 dispersion Substances 0.000 description 6
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- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 6
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- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
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- 159000000000 sodium salts Chemical class 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 241001480061 Blumeria graminis Species 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
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- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 2
- YTOPFCCWCSOHFV-UHFFFAOYSA-N 2,6-dimethyl-4-tridecylmorpholine Chemical compound CCCCCCCCCCCCCN1CC(C)OC(C)C1 YTOPFCCWCSOHFV-UHFFFAOYSA-N 0.000 description 2
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 240000007154 Coffea arabica Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 240000009088 Fragaria x ananassa Species 0.000 description 2
- PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 2
- 240000000111 Saccharum officinarum Species 0.000 description 2
- 235000007201 Saccharum officinarum Nutrition 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 241000221577 Uromyces appendiculatus Species 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 159000000007 calcium salts Chemical class 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 235000016213 coffee Nutrition 0.000 description 2
- 235000013353 coffee beverage Nutrition 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000012990 dithiocarbamate Substances 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000446 fuel Substances 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 2
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- 239000000843 powder Substances 0.000 description 2
- UFUASNAHBMBJIX-UHFFFAOYSA-N propan-1-one Chemical compound CC[C]=O UFUASNAHBMBJIX-UHFFFAOYSA-N 0.000 description 2
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- 235000021012 strawberries Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 2
- 239000002699 waste material Substances 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
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- 125000001376 1,2,4-triazolyl group Chemical group N1N=C(N=C1)* 0.000 description 1
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 1
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- OZOMQRBLCMDCEG-VIZOYTHASA-N 1-[(e)-[5-(4-nitrophenyl)furan-2-yl]methylideneamino]imidazolidine-2,4-dione Chemical compound C1=CC([N+](=O)[O-])=CC=C1C(O1)=CC=C1\C=N\N1C(=O)NC(=O)C1 OZOMQRBLCMDCEG-VIZOYTHASA-N 0.000 description 1
- HMUNWXXNJPVALC-UHFFFAOYSA-N 1-[4-[2-(2,3-dihydro-1H-inden-2-ylamino)pyrimidin-5-yl]piperazin-1-yl]-2-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)ethanone Chemical compound C1C(CC2=CC=CC=C12)NC1=NC=C(C=N1)N1CCN(CC1)C(CN1CC2=C(CC1)NN=N2)=O HMUNWXXNJPVALC-UHFFFAOYSA-N 0.000 description 1
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 description 1
- KBLAMUYRMZPYLS-UHFFFAOYSA-N 2,3-bis(2-methylpropyl)naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(CC(C)C)C(CC(C)C)=CC2=C1 KBLAMUYRMZPYLS-UHFFFAOYSA-N 0.000 description 1
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- 239000007789 gas Substances 0.000 description 1
- DDUHZTYCFQRHIY-RBHXEPJQSA-N griseofulvin Chemical compound COC1=CC(=O)C[C@@H](C)[C@@]11C(=O)C(C(OC)=CC(OC)=C2Cl)=C2O1 DDUHZTYCFQRHIY-RBHXEPJQSA-N 0.000 description 1
- 229960002867 griseofulvin Drugs 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 150000003840 hydrochlorides Chemical class 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- 239000003701 inert diluent Substances 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[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
- 239000000463 material Substances 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- HAMGRBXTJNITHG-UHFFFAOYSA-N methyl isocyanate Chemical compound CN=C=O HAMGRBXTJNITHG-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 1
- OYRIKLVYHTWHCZ-UHFFFAOYSA-N n-cyclohexyl-2,5-dimethylfuran-3-carboxamide Chemical compound O1C(C)=CC(C(=O)NC2CCCCC2)=C1C OYRIKLVYHTWHCZ-UHFFFAOYSA-N 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 125000002868 norbornyl group Chemical group C12(CCC(CC1)C2)* 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical group C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000012074 organic phase Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000003891 oxalate salts Chemical class 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 description 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000002244 precipitate Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- FGVVTMRZYROCTH-UHFFFAOYSA-N pyridine-2-thiol N-oxide Chemical compound [O-][N+]1=CC=CC=C1S FGVVTMRZYROCTH-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 238000009938 salting Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-UHFFFAOYSA-N 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 210000002105 tongue Anatomy 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 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
-
- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- 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
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Priority Applications (18)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762634511 DE2634511A1 (de) | 1976-07-31 | 1976-07-31 | Beta-azolylketone |
| AU25959/77A AU512537B2 (en) | 1976-07-31 | 1977-06-08 | Beta-azolyl ketones |
| CA282,225A CA1095054A (en) | 1976-07-31 | 1977-07-07 | .beta.-AZOLYLKETONES |
| CS473577A CS193582B2 (en) | 1976-07-31 | 1977-07-15 | Fingicide means |
| IT5041777A IT1079805B (it) | 1976-07-31 | 1977-07-25 | Beta-azolilchetoni |
| CH930477A CH629079A5 (en) | 1976-07-31 | 1977-07-27 | Fungicide |
| FR7723249A FR2360583A1 (fr) | 1976-07-31 | 1977-07-28 | B-azolylcetones utiles comme fongicides |
| PL19990677A PL103010B1 (pl) | 1976-07-31 | 1977-07-28 | Srodek grzybobojczy |
| NZ18477377A NZ184773A (en) | 1976-07-31 | 1977-07-28 | -1,2,4-triazol-1-yl ketones and fungicides |
| SE7708690A SE427110B (sv) | 1976-07-31 | 1977-07-28 | Forening till anvendning som fungicid |
| GB3192677A GB1580389A (en) | 1976-07-31 | 1977-07-29 | azolyl ketones and their use as fungicides |
| DD20035377A DD130440A5 (de) | 1976-07-31 | 1977-07-29 | Fungizide mittel |
| BE179760A BE857300A (fr) | 1976-07-31 | 1977-07-29 | B-azolylcetones utiles comme fongicides |
| NL7708444A NL7708444A (nl) | 1976-07-31 | 1977-07-29 | Werkwijze voor de bereiding van (beta)-azolylketonen. |
| AT561877A AT355868B (de) | 1976-07-31 | 1977-07-29 | Fungizid |
| SU772506703A SU663264A3 (ru) | 1976-07-31 | 1977-07-29 | Фунгицидный состав |
| DK342177A DK146026C (da) | 1976-07-31 | 1977-07-29 | Beta-azolylketoner med fungicid virkning |
| HU77BA3564A HU176920B (hu) | 1976-07-31 | 1977-07-31 | Fungicidnye kompozicii soderzhahhie beta-triazolil-ketony i soli,i sposob poluchenija beta-triazolil-ketonov |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19762634511 DE2634511A1 (de) | 1976-07-31 | 1976-07-31 | Beta-azolylketone |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2634511A1 true DE2634511A1 (de) | 1978-02-02 |
Family
ID=5984402
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19762634511 Withdrawn DE2634511A1 (de) | 1976-07-31 | 1976-07-31 | Beta-azolylketone |
Country Status (18)
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0007010A1 (de) * | 1978-06-19 | 1980-01-23 | Hoechst Aktiengesellschaft | 1,2,4-Triazolderivate, Verfahren zu deren Herstellung, deren Verwendung als Schädlingsbekämpfungsmittel und Pflanzenwuchsregulatoren und diese Derivate enthaltende Schädlingsbekämpfungsmittel |
| EP0009740A1 (de) * | 1978-09-30 | 1980-04-16 | BASF Aktiengesellschaft | Beta-Triazolyloxime, diese enthaltende Mittel zur Beeinflussung des Pflanzenwachstums und ihre Anwendung |
| EP0010674A1 (de) * | 1978-10-28 | 1980-05-14 | Bayer Ag | Neue Ethen-azol-Derivate, Verfahren zu ihrer Herstellung, fungizide Mittel, Verfahren zur Herstellung dieser sowie Verwendung der Azol-Derivate zur Bekämpfung von Pilzen und ein Verfahren zur Bekämpfung von Pilzen |
| EP0019762A1 (de) * | 1979-05-25 | 1980-12-10 | BASF Aktiengesellschaft | Triazolylderivate, Verfahren zu ihrer Herstellung sowie diese enthaltende Mittel zur Beeinflussung des Pflanzenwachstums |
| EP0037468A3 (de) * | 1980-03-24 | 1981-10-21 | BASF Aktiengesellschaft | Verfahren zur Bekämpfunng von Pilzen mit Triatolylderivaten |
| US4328028A (en) | 1977-08-27 | 1982-05-04 | Basf Aktiengesellschaft | Plant growth regulators |
| EP0062236A3 (en) * | 1981-04-04 | 1983-08-17 | Basf Aktiengesellschaft | Fungicidal agent containing triazole derivatives, and process for combating fungi therewith |
| US4532234A (en) * | 1982-09-07 | 1985-07-30 | Basf Aktiengesellschaft | Neopentyl-phenethyltriazoles, their preparation and fungicides containing these compounds |
| EP0297352A1 (de) * | 1987-06-27 | 1989-01-04 | Bayer Ag | (Azolyl-vinyl)-phenol-alkenylether |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8093279B2 (en) | 2005-12-13 | 2012-01-10 | Gillian Reed, legal representative | Compound |
| GB0525323D0 (en) | 2005-12-13 | 2006-01-18 | Sterix Ltd | Compound |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1492882A (en) * | 1975-10-06 | 1977-11-23 | Ici Ltd | Alpha-1,2,4-triazolyl-2-acetylthiophenes and their use as pesticides |
-
1976
- 1976-07-31 DE DE19762634511 patent/DE2634511A1/de not_active Withdrawn
-
1977
- 1977-06-08 AU AU25959/77A patent/AU512537B2/en not_active Expired
- 1977-07-07 CA CA282,225A patent/CA1095054A/en not_active Expired
- 1977-07-15 CS CS473577A patent/CS193582B2/cs unknown
- 1977-07-25 IT IT5041777A patent/IT1079805B/it active
- 1977-07-27 CH CH930477A patent/CH629079A5/de not_active IP Right Cessation
- 1977-07-28 PL PL19990677A patent/PL103010B1/xx unknown
- 1977-07-28 SE SE7708690A patent/SE427110B/xx not_active IP Right Cessation
- 1977-07-28 FR FR7723249A patent/FR2360583A1/fr active Granted
- 1977-07-28 NZ NZ18477377A patent/NZ184773A/xx unknown
- 1977-07-29 DD DD20035377A patent/DD130440A5/xx unknown
- 1977-07-29 SU SU772506703A patent/SU663264A3/ru active
- 1977-07-29 BE BE179760A patent/BE857300A/xx not_active IP Right Cessation
- 1977-07-29 AT AT561877A patent/AT355868B/de not_active IP Right Cessation
- 1977-07-29 GB GB3192677A patent/GB1580389A/en not_active Expired
- 1977-07-29 DK DK342177A patent/DK146026C/da not_active IP Right Cessation
- 1977-07-29 NL NL7708444A patent/NL7708444A/xx not_active Application Discontinuation
- 1977-07-31 HU HU77BA3564A patent/HU176920B/hu unknown
Cited By (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4328028A (en) | 1977-08-27 | 1982-05-04 | Basf Aktiengesellschaft | Plant growth regulators |
| EP0007010A1 (de) * | 1978-06-19 | 1980-01-23 | Hoechst Aktiengesellschaft | 1,2,4-Triazolderivate, Verfahren zu deren Herstellung, deren Verwendung als Schädlingsbekämpfungsmittel und Pflanzenwuchsregulatoren und diese Derivate enthaltende Schädlingsbekämpfungsmittel |
| EP0009740A1 (de) * | 1978-09-30 | 1980-04-16 | BASF Aktiengesellschaft | Beta-Triazolyloxime, diese enthaltende Mittel zur Beeinflussung des Pflanzenwachstums und ihre Anwendung |
| US4684392A (en) * | 1978-09-30 | 1987-08-04 | Basf Aktiengesellschaft | Beta-triazolyl oximes agents containing them for influencing the growth of plants and their use |
| EP0010674A1 (de) * | 1978-10-28 | 1980-05-14 | Bayer Ag | Neue Ethen-azol-Derivate, Verfahren zu ihrer Herstellung, fungizide Mittel, Verfahren zur Herstellung dieser sowie Verwendung der Azol-Derivate zur Bekämpfung von Pilzen und ein Verfahren zur Bekämpfung von Pilzen |
| EP0019762A1 (de) * | 1979-05-25 | 1980-12-10 | BASF Aktiengesellschaft | Triazolylderivate, Verfahren zu ihrer Herstellung sowie diese enthaltende Mittel zur Beeinflussung des Pflanzenwachstums |
| US4319911A (en) * | 1979-05-25 | 1982-03-16 | Basf Aktiengesellschaft | Triazolyl derivatives, their manufacture, and agents containing them for influencing plant growth |
| EP0037468A3 (de) * | 1980-03-24 | 1981-10-21 | BASF Aktiengesellschaft | Verfahren zur Bekämpfunng von Pilzen mit Triatolylderivaten |
| EP0062236A3 (en) * | 1981-04-04 | 1983-08-17 | Basf Aktiengesellschaft | Fungicidal agent containing triazole derivatives, and process for combating fungi therewith |
| US4532234A (en) * | 1982-09-07 | 1985-07-30 | Basf Aktiengesellschaft | Neopentyl-phenethyltriazoles, their preparation and fungicides containing these compounds |
| EP0297352A1 (de) * | 1987-06-27 | 1989-01-04 | Bayer Ag | (Azolyl-vinyl)-phenol-alkenylether |
| US4894381A (en) * | 1987-06-27 | 1990-01-16 | Bayer Aktiengesellschaft | Microbicidal (azolyl-vinyl)-phenol alkenyl ethers |
Also Published As
| Publication number | Publication date |
|---|---|
| SE427110B (sv) | 1983-03-07 |
| BE857300A (fr) | 1978-01-30 |
| AU512537B2 (en) | 1980-10-16 |
| NL7708444A (nl) | 1978-02-02 |
| FR2360583A1 (fr) | 1978-03-03 |
| DK146026C (da) | 1985-02-04 |
| GB1580389A (en) | 1980-12-03 |
| IT1079805B (it) | 1985-05-13 |
| SU663264A3 (ru) | 1979-05-15 |
| DK342177A (da) | 1978-02-01 |
| HU176920B (hu) | 1981-06-28 |
| DK146026B (da) | 1983-05-30 |
| PL199906A1 (pl) | 1978-04-10 |
| DD130440A5 (de) | 1978-04-05 |
| CS193582B2 (en) | 1979-10-31 |
| ATA561877A (de) | 1979-08-15 |
| AT355868B (de) | 1980-03-25 |
| AU2595977A (en) | 1978-12-14 |
| CH629079A5 (en) | 1982-04-15 |
| PL103010B1 (pl) | 1979-05-31 |
| NZ184773A (en) | 1979-10-25 |
| FR2360583B1 (enrdf_load_stackoverflow) | 1981-06-19 |
| CA1095054A (en) | 1981-02-03 |
| SE7708690L (sv) | 1978-02-01 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8141 | Disposal/no request for examination |