JPS6010003B2 - 殺かび組成物 - Google Patents
殺かび組成物Info
- Publication number
- JPS6010003B2 JPS6010003B2 JP49070743A JP7074374A JPS6010003B2 JP S6010003 B2 JPS6010003 B2 JP S6010003B2 JP 49070743 A JP49070743 A JP 49070743A JP 7074374 A JP7074374 A JP 7074374A JP S6010003 B2 JPS6010003 B2 JP S6010003B2
- Authority
- JP
- Japan
- Prior art keywords
- group
- imidazole
- formula
- compound
- compounds
- 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims description 39
- 230000000855 fungicidal effect Effects 0.000 title description 8
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 22
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 3
- 239000000126 substance Substances 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 2
- 125000001475 halogen functional group Chemical group 0.000 claims 2
- 230000000844 anti-bacterial effect Effects 0.000 claims 1
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 92
- 150000001875 compounds Chemical class 0.000 description 59
- -1 n-octyl group Chemical group 0.000 description 35
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 26
- 150000002460 imidazoles Chemical class 0.000 description 22
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 21
- 239000002904 solvent Substances 0.000 description 17
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- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 15
- 241000209219 Hordeum Species 0.000 description 15
- 235000007340 Hordeum vulgare Nutrition 0.000 description 15
- 241000221785 Erysiphales Species 0.000 description 14
- 239000000243 solution Substances 0.000 description 14
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 12
- 239000004480 active ingredient Substances 0.000 description 12
- 125000004432 carbon atom Chemical group C* 0.000 description 12
- 150000002367 halogens Chemical class 0.000 description 12
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- 239000000543 intermediate Substances 0.000 description 11
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- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 10
- 235000013339 cereals Nutrition 0.000 description 10
- 229910052736 halogen Inorganic materials 0.000 description 10
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- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 6
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
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- 239000003208 petroleum Substances 0.000 description 6
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- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical compound CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 6
- CKDWPUIZGOQOOM-UHFFFAOYSA-N Carbamyl chloride Chemical compound NC(Cl)=O CKDWPUIZGOQOOM-UHFFFAOYSA-N 0.000 description 5
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- 125000005843 halogen group Chemical group 0.000 description 5
- 239000000376 reactant Substances 0.000 description 5
- 239000011541 reaction mixture Substances 0.000 description 5
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 5
- 241000209761 Avena Species 0.000 description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 4
- 125000000304 alkynyl group Chemical group 0.000 description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
- 229910052794 bromium Inorganic materials 0.000 description 4
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- 239000003595 mist Substances 0.000 description 4
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- 239000007921 spray Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 239000008096 xylene Substances 0.000 description 4
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- 244000075850 Avena orientalis Species 0.000 description 3
- 235000007558 Avena sp Nutrition 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 3
- 238000001816 cooling Methods 0.000 description 3
- 235000013399 edible fruits Nutrition 0.000 description 3
- 230000008020 evaporation Effects 0.000 description 3
- 239000004615 ingredient Substances 0.000 description 3
- 239000010410 layer Substances 0.000 description 3
- OSYXPCGQYBKLJP-UHFFFAOYSA-N n-[(4-chlorophenyl)methyl]-n-propylcarbamoyl chloride Chemical compound CCCN(C(Cl)=O)CC1=CC=C(Cl)C=C1 OSYXPCGQYBKLJP-UHFFFAOYSA-N 0.000 description 3
- 125000003884 phenylalkyl group Chemical group 0.000 description 3
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 3
- 229910052938 sodium sulfate Inorganic materials 0.000 description 3
- 235000011152 sodium sulphate Nutrition 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 150000003512 tertiary amines Chemical class 0.000 description 3
- CYNYIHKIEHGYOZ-UHFFFAOYSA-N 1-bromopropane Chemical compound CCCBr CYNYIHKIEHGYOZ-UHFFFAOYSA-N 0.000 description 2
- JDIIGWSSTNUWGK-UHFFFAOYSA-N 1h-imidazol-3-ium;chloride Chemical compound [Cl-].[NH2+]1C=CN=C1 JDIIGWSSTNUWGK-UHFFFAOYSA-N 0.000 description 2
- NMIZONYLXCOHEF-UHFFFAOYSA-N 1h-imidazole-2-carboxamide Chemical class NC(=O)C1=NC=CN1 NMIZONYLXCOHEF-UHFFFAOYSA-N 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- 235000009849 Cucumis sativus Nutrition 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 230000000895 acaricidal effect Effects 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 235000012211 aluminium silicate Nutrition 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- GRSTVVGJSKHCCS-UHFFFAOYSA-N bis(1h-imidazol-2-yl)methanone Chemical compound N=1C=CNC=1C(=O)C1=NC=CN1 GRSTVVGJSKHCCS-UHFFFAOYSA-N 0.000 description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 2
- 150000007942 carboxylates Chemical class 0.000 description 2
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
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- 238000010410 dusting Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 239000012433 hydrogen halide Substances 0.000 description 2
- 229910000039 hydrogen halide Inorganic materials 0.000 description 2
- 238000011081 inoculation Methods 0.000 description 2
- 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 2
- 210000002414 leg Anatomy 0.000 description 2
- 125000005394 methallyl group Chemical group 0.000 description 2
- SYJZOOYUIXOMRE-UHFFFAOYSA-N n-(2-chlorophenyl)-n-propylcarbamoyl chloride Chemical compound CCCN(C(Cl)=O)C1=CC=CC=C1Cl SYJZOOYUIXOMRE-UHFFFAOYSA-N 0.000 description 2
- IIAGANUYLNPJEW-UHFFFAOYSA-N n-(2-fluorophenyl)-n-propylimidazole-1-carboxamide Chemical compound C=1C=CC=C(F)C=1N(CCC)C(=O)N1C=CN=C1 IIAGANUYLNPJEW-UHFFFAOYSA-N 0.000 description 2
- GQHBLENCCBUDHQ-UHFFFAOYSA-N n-(2-phenoxyethyl)-n-propylcarbamoyl chloride Chemical compound CCCN(C(Cl)=O)CCOC1=CC=CC=C1 GQHBLENCCBUDHQ-UHFFFAOYSA-N 0.000 description 2
- MLGQEPMFXRBWSX-UHFFFAOYSA-N n-[(2-chlorophenyl)methyl]-n-(2-phenylethyl)imidazole-1-carboxamide Chemical compound ClC1=CC=CC=C1CN(C(=O)N1C=NC=C1)CCC1=CC=CC=C1 MLGQEPMFXRBWSX-UHFFFAOYSA-N 0.000 description 2
- RCIHELJWBJHVBL-UHFFFAOYSA-N n-[(4-chlorophenyl)methyl]-n-cyclooctylimidazole-1-carboxamide Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)N1C=NC=C1)C1CCCCCCC1 RCIHELJWBJHVBL-UHFFFAOYSA-N 0.000 description 2
- ZZDMTQUDHVPBHC-UHFFFAOYSA-N n-[(4-chlorophenyl)methyl]propan-1-amine Chemical compound CCCNCC1=CC=C(Cl)C=C1 ZZDMTQUDHVPBHC-UHFFFAOYSA-N 0.000 description 2
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- 125000002435 L-phenylalanyl group Chemical group O=C([*])[C@](N([H])[H])([H])C([H])([H])C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
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- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 239000011928 denatured alcohol Substances 0.000 description 1
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- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
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- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- ZNOLGFHPUIJIMJ-UHFFFAOYSA-N fenitrothion Chemical compound COP(=S)(OC)OC1=CC=C([N+]([O-])=O)C(C)=C1 ZNOLGFHPUIJIMJ-UHFFFAOYSA-N 0.000 description 1
- 229910052731 fluorine Inorganic materials 0.000 description 1
- 239000011737 fluorine Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- OCDGBSUVYYVKQZ-UHFFFAOYSA-N gramine Chemical compound C1=CC=C2C(CN(C)C)=CNC2=C1 OCDGBSUVYYVKQZ-UHFFFAOYSA-N 0.000 description 1
- GOERTRUXQHDLHC-UHFFFAOYSA-N gramine Natural products COC1=CC=C2NC=C(CN(C)C)C2=C1 GOERTRUXQHDLHC-UHFFFAOYSA-N 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
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- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 229940072322 hylan Drugs 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
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- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 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
- 239000012948 isocyanate Substances 0.000 description 1
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- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 150000004668 long chain fatty acids Chemical class 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 239000002362 mulch Substances 0.000 description 1
- FGLPQNVGEHUHCI-UHFFFAOYSA-N n-(2-chlorophenyl)-n-propan-2-ylimidazole-1-carboxamide Chemical compound C=1C=CC=C(Cl)C=1N(C(C)C)C(=O)N1C=CN=C1 FGLPQNVGEHUHCI-UHFFFAOYSA-N 0.000 description 1
- UHWJMNBUXCZKDL-UHFFFAOYSA-N n-(2-chlorophenyl)-n-propylimidazole-1-carboxamide Chemical compound C=1C=CC=C(Cl)C=1N(CCC)C(=O)N1C=CN=C1 UHWJMNBUXCZKDL-UHFFFAOYSA-N 0.000 description 1
- KGHKGNUKEKEIBR-UHFFFAOYSA-N n-(2-phenoxyethyl)-n-propylimidazole-1-carboxamide Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=CC=CC=C1 KGHKGNUKEKEIBR-UHFFFAOYSA-N 0.000 description 1
- LNAITMPDHGSOKD-UHFFFAOYSA-N n-(4-chlorophenyl)-n-propylimidazole-1-carboxamide Chemical compound C=1C=C(Cl)C=CC=1N(CCC)C(=O)N1C=CN=C1 LNAITMPDHGSOKD-UHFFFAOYSA-N 0.000 description 1
- JAFFOSZVIPMBKE-UHFFFAOYSA-N n-[(4-chlorophenyl)methyl]-n-propylimidazole-1-carboxamide Chemical compound C1=CN=CN1C(=O)N(CCC)CC1=CC=C(Cl)C=C1 JAFFOSZVIPMBKE-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000003136 n-heptyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000005609 naphthenate group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 150000004045 organic chlorine compounds Chemical class 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 125000005359 phenoxyalkyl group Chemical group 0.000 description 1
- 125000004344 phenylpropyl group Chemical group 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 239000001205 polyphosphate Substances 0.000 description 1
- 235000011176 polyphosphates Nutrition 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 235000015136 pumpkin Nutrition 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000000926 separation method Methods 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
- 239000012312 sodium hydride Substances 0.000 description 1
- 229910000104 sodium hydride Inorganic materials 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical class CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 210000000689 upper leg Anatomy 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 235000015099 wheat brans Nutrition 0.000 description 1
- JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues 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)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB2953573A GB1469772A (en) | 1973-06-21 | 1973-06-21 | Fungicidal imidazole derivatives |
| GB29535/73 | 1973-06-21 | ||
| AU76526/74A AU491880B2 (en) | 1973-06-21 | 1974-12-17 | Imidazole derivatives having fungicidal properties |
| ZA00748037A ZA748037B (en) | 1973-06-21 | 1974-12-18 | Fungicidal compositions |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5031047A JPS5031047A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1975-03-27 |
| JPS6010003B2 true JPS6010003B2 (ja) | 1985-03-14 |
Family
ID=27156206
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP49070743A Expired JPS6010003B2 (ja) | 1973-06-21 | 1974-06-20 | 殺かび組成物 |
Country Status (14)
Families Citing this family (97)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4041019A (en) * | 1975-10-22 | 1977-08-09 | The Dow Chemical Company | Delayed-action, heat activated-urethane catalyst |
| GB1572348A (en) | 1976-04-10 | 1980-07-30 | Boots Co Ltd | Method of regulating plant growth |
| GB1567521A (en) | 1977-03-26 | 1980-05-14 | Boots Co Ltd | Funigicidal complexes of metal salts with imidazoles |
| NZ188742A (en) * | 1977-10-26 | 1981-03-16 | Wellcome Found | Imidazolines and pesticidal compositions |
| ZA787351B (en) * | 1978-06-19 | 1980-08-27 | Wellcome Found | Imidazolines,their preparation,intermediates therefor,and pesticidal formulations and use of the imidazolines |
| FR2466952A1 (fr) * | 1979-10-12 | 1981-04-17 | Boots Co Ltd | Composition fongicide a base de prochloraz et ses applications |
| FR2499077A1 (fr) * | 1981-02-05 | 1982-08-06 | Ciba Geigy Ag | Derives de l'aniline, leur preparation et produits microbicides en contenant |
| JPS57175105A (en) * | 1981-04-20 | 1982-10-28 | Ube Ind Ltd | Fungicide for agricultural and horticultural purpose |
| AU553831B2 (en) * | 1982-03-04 | 1986-07-31 | Nippon Kayaku Kabushiki Kaisha | N,n-disubstituted azolecarboxamides |
| DE3235050A1 (de) * | 1982-09-22 | 1984-03-22 | Bayer Ag, 5090 Leverkusen | Fungizide mittel |
| US4504484A (en) * | 1982-11-04 | 1985-03-12 | Chevron Research Company | Certain N,N-di-substituted-pyridine carboxamides, fungicidal compositions and fungicidal method of use |
| US4654346A (en) * | 1982-11-04 | 1987-03-31 | Chevron Research Company | Fungicidal N,N-disubstituted-heterocyclic carboxamides |
| US4782074A (en) * | 1982-11-04 | 1988-11-01 | Chevron Research Company | Fungicidal N,N-disubstituted-heterocyclic carboxamides |
| US4661494A (en) * | 1982-12-03 | 1987-04-28 | Chevron Research Company | N-substituted-N',N'-disubstituted glycinamide fungicides |
| US4579856A (en) * | 1983-09-23 | 1986-04-01 | Chevron Research Company | Fungicidal N-pyridyloxyalkyl amides |
| JPS60109568A (ja) * | 1983-11-17 | 1985-06-15 | Ube Ind Ltd | イミダゾ−ル誘導体および農園芸用殺菌剤 |
| GB8403726D0 (en) * | 1984-02-13 | 1984-03-14 | Shell Int Research | Carboxamide derivatives |
| DE3411388A1 (de) * | 1984-03-28 | 1985-10-10 | Basf Ag, 6700 Ludwigshafen | Vinyl-azolylharnstoffe und diese enthaltende fungizide |
| DE3415139A1 (de) * | 1984-04-21 | 1985-10-31 | Basf Ag, 6700 Ludwigshafen | N-(arylpropyl)-azolylharnstoffe und diese enthaltende pungizide |
| EP0175188A1 (de) * | 1984-09-11 | 1986-03-26 | Nihon Tokushu Noyaku Seizo K.K. | Carbamoylimidazol-Derivate |
| DE3507630A1 (de) * | 1985-03-05 | 1986-09-11 | Basf Ag, 6700 Ludwigshafen | N-(cycloalkoxyalkyl)-azolylharnstoffe und diese enthaltende fungizide |
| DE3513259A1 (de) * | 1985-04-13 | 1986-10-23 | Bayer Ag, 5090 Leverkusen | Heterocyclische amid-derivate |
| DE3614608A1 (de) * | 1986-04-30 | 1987-11-05 | Basf Ag | Aryloxycarbamoylazole und diese enthaltende fungizide |
| DE3704262A1 (de) * | 1987-02-12 | 1988-08-25 | Bayer Ag | Verwendung von azolylmethyl-cyclopropylcarbinol-derivaten zur bekaempfung von pseudocercosporella herpotrichoides |
| WO1988007813A1 (en) * | 1987-04-14 | 1988-10-20 | Greencare Pty. Limited | Soil spreader |
| JPH01203367A (ja) * | 1988-02-05 | 1989-08-16 | Otsuka Chem Co Ltd | イミダゾール誘導体及び農園芸用殺菌剤 |
| IL90704A (en) * | 1989-06-21 | 1994-10-07 | Makhteshim Chem Works Ltd | Method for the preparation of N-N-) 2,4,6-trichlorophenoxy (environmentally reliable ethylene) |
| HU207702B (en) * | 1989-06-21 | 1993-05-28 | Makhteshim Chem Works Ltd | Process for producing n-/n-propyl/-n/2-/2,4,6-trichloro-phenoxy/-ethyl/-amine |
| IL90703A (en) * | 1989-06-21 | 1994-10-07 | Makhteshim Chem Works Ltd | Method of preparing n-n-propyl-n-2-(2,4,6-trichlorophenoxy)-ethyl amine |
| EP0454492B1 (en) * | 1990-04-26 | 1995-06-21 | Mitsubishi Gas Chemical Company, Inc. | N-benzyl-N-phenoxyethylamines and agricultural and horticultural bactericides |
| DE4108871A1 (de) * | 1991-03-19 | 1992-09-24 | Hoechst Ag | Waessrige formulierung von prochloraz, ihre herstellung und ihre verwendung |
| US5531995A (en) * | 1992-10-29 | 1996-07-02 | Makhteshim Chemical Works Ltd. | Low ecotoxic formulations of pesticides |
| CH686061A5 (de) * | 1993-06-04 | 1995-12-29 | Ciba Geigy Ag | Mikrobizide. |
| EP0645091B1 (de) * | 1993-09-24 | 1996-04-17 | BASF Aktiengesellschaft | Fungizide Mischungen |
| FR2732190B1 (fr) * | 1995-04-03 | 1997-04-30 | Rhone Poulenc Agrochimie | Composition fongicide a base de prochloraze et d'un compose triazole |
| JPH0940513A (ja) * | 1995-07-28 | 1997-02-10 | Hoechst Schering Agrevo Kk | 農業用殺菌剤 |
| DE19547627C2 (de) * | 1995-09-21 | 2002-05-16 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| US5696150A (en) * | 1995-09-21 | 1997-12-09 | Bayer Aktiengesellschaft | Fungicidal active compound combinations |
| CA2278179A1 (en) * | 1997-01-17 | 1998-07-23 | Ppg Industries, Inc. | Method of producing n,n'-diazole compounds |
| DE19830556A1 (de) | 1998-07-08 | 2000-01-13 | Basf Ag | Verfahren zur Herstellung von Carbonyldiimidazolen |
| US6639109B1 (en) | 1999-09-28 | 2003-10-28 | Nihon Nohyaku Co., Ltd. | Process for production of thioalkylamine derivatives |
| MXPA02005835A (es) * | 1999-12-13 | 2003-01-28 | Bayer Ag | Combinaciones de productos activos fungicidas. |
| DE10019758A1 (de) * | 2000-04-20 | 2001-10-25 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| DE10103832A1 (de) * | 2000-05-11 | 2001-11-15 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| DE10049804A1 (de) * | 2000-10-09 | 2002-04-18 | Bayer Ag | Wirkstoffkombinationen mit fungiziden und akariziden Eigenschaften |
| DE10105077A1 (de) * | 2001-02-05 | 2002-08-08 | Febit Ferrarius Biotech Gmbh | Hybrid-Schutzgruppe |
| US6455702B1 (en) * | 2001-05-16 | 2002-09-24 | Aims Fine Chemicals, Inc. | Process for the production of N,N-carbonyl diimidazole |
| DE10141618A1 (de) * | 2001-08-24 | 2003-03-06 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| JP4722398B2 (ja) | 2002-03-21 | 2011-07-13 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌性混合物 |
| JP2005527568A (ja) * | 2002-04-05 | 2005-09-15 | ビーエーエスエフ アクチェンゲゼルシャフト | ベンズアミドキシム誘導体とアゾールに基づく殺真菌性混合物 |
| DE10239480A1 (de) * | 2002-08-28 | 2004-03-04 | Bayer Cropscience Ag | Tetrahydropyridazin-Derivate |
| PT1562429E (pt) * | 2002-11-12 | 2008-10-08 | Basf Se | Processo para aumentar o rendimento em leguminosas resistentes ao glifosato |
| EA200500722A1 (ru) * | 2002-11-15 | 2005-12-29 | Басф Акциенгезельшафт | Фунгицидные смеси на основе триазолопиримидинов и азолов |
| DE10347090A1 (de) | 2003-10-10 | 2005-05-04 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE10349501A1 (de) | 2003-10-23 | 2005-05-25 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| US20050171172A1 (en) * | 2003-11-13 | 2005-08-04 | Ambit Biosciences Corporation | Amide derivatives as PDGFR modulators |
| WO2005104847A1 (de) | 2004-04-30 | 2005-11-10 | Basf Aktiengesellschaft | Fungizide mischungen |
| DE102004049761A1 (de) | 2004-10-12 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| DE102005015677A1 (de) * | 2005-04-06 | 2006-10-12 | Bayer Cropscience Ag | Synergistische fungizide Wirkstoffkombinationen |
| DE102005026482A1 (de) | 2005-06-09 | 2006-12-14 | Bayer Cropscience Ag | Wirkstoffkombinationen |
| BRPI0612022B1 (pt) | 2005-06-09 | 2016-12-06 | Bayer Cropscience Ag | combinações de substâncias ativas, seus usos, processos para combater fungos fitopatogênicos indesejáveis, processo para preparar composições fungicidas, revestimento de semente, e processos para revestir semente e semente transgênica |
| SI1912503T1 (sl) | 2005-08-05 | 2014-09-30 | Basf Se | Fungicidne mešanice, ki vsebujejo 1-metilpirazol-4IL karboksilične kislinske anilide |
| RU2329646C2 (ru) * | 2005-08-18 | 2008-07-27 | Российский химико-технологический университет (РХТУ им. Д.И. Менделеева) | Применение замещенных 1-(2-феноксиэтил)-1,2,4-триазолов в качестве фунгицидных средств и фунгицидная композиция на их основе |
| DE102006023263A1 (de) | 2006-05-18 | 2007-11-22 | Bayer Cropscience Ag | Synergistische Wirkstoffkombinationen |
| BRPI0716915B1 (pt) | 2006-09-18 | 2016-09-13 | Basf Se | mistura pesticida, composição pesticida, métodos para controlar fungos nocivos fitopatogênicos, para controlar insetos, aracnídeos ou nematódeos, para proteger plantas e para proteger semente, processo para a preparação de uma composição, e uso de uma mistura |
| WO2008071714A1 (en) | 2006-12-15 | 2008-06-19 | Rohm And Haas Company | Mixtures comprising 1-methylcyclopropene |
| AU2008206997A1 (en) * | 2007-01-17 | 2008-07-24 | Basf Se | Method, use and agent for protecting a plant against Pythium and Rhizoctonia |
| CN101605461A (zh) * | 2007-02-06 | 2009-12-16 | 巴斯夫欧洲公司 | 农药混合物 |
| US20100093715A1 (en) | 2007-04-23 | 2010-04-15 | Basf Se | Plant productivity enhancement by combining chemical agents with transgenic modifications |
| CN101668427A (zh) * | 2007-04-25 | 2010-03-10 | 巴斯夫欧洲公司 | 杀真菌剂混合物 |
| DE102007045920B4 (de) | 2007-09-26 | 2018-07-05 | Bayer Intellectual Property Gmbh | Synergistische Wirkstoffkombinationen |
| PL2205082T3 (pl) | 2007-09-26 | 2012-08-31 | Basf Se | Trójskładnikowe kompozycje grzybobójcze zawierające boskalid i chlorotalonil |
| JP5502854B2 (ja) * | 2008-05-08 | 2014-05-28 | ビーエーエスエフ ソシエタス・ヨーロピア | 菌類感染から大豆を保護する方法 |
| JP5530428B2 (ja) * | 2008-07-04 | 2014-06-25 | ビーエーエスエフ ソシエタス・ヨーロピア | 置換１−メチルピラゾール−４−イルカルボキシアニリドを含んでいる殺菌剤混合物 |
| CN101402608B (zh) * | 2008-11-25 | 2011-11-02 | 乐斯化学有限公司 | 一种杀菌剂咪鲜胺的生产方法 |
| US9012360B2 (en) | 2009-03-25 | 2015-04-21 | Bayer Intellectual Property Gmbh | Synergistic combinations of active ingredients |
| WO2011006886A2 (en) | 2009-07-14 | 2011-01-20 | Basf Se | Azole compounds carrying a sulfur substituent xiv |
| JP5642786B2 (ja) | 2009-07-16 | 2014-12-17 | バイエル・クロップサイエンス・アーゲーＢａｙｅｒ Ｃｒｏｐｓｃｉｅｎｃｅ Ａｇ | フェニルトリアゾール類を含む相乗的活性化合物組み合わせ |
| WO2011026796A1 (en) | 2009-09-01 | 2011-03-10 | Basf Se | Synergistic fungicidal mixtures comprising lactylates and method for combating phytopathogenic fungi |
| KR20130132942A (ko) | 2010-12-20 | 2013-12-05 | 바스프 에스이 | 피라졸 화합물을 포함하는 살충 활성 혼합물 |
| EP2481284A3 (en) | 2011-01-27 | 2012-10-17 | Basf Se | Pesticidal mixtures |
| EP3378313A1 (en) | 2011-03-23 | 2018-09-26 | Basf Se | Compositions containing polymeric, ionic compounds comprising imidazolium groups |
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| MX2014001866A (es) | 2011-09-02 | 2015-04-16 | Basf Se | Mezclas agricolas que comprenden compuestos de arilquinazolinona. |
| CN102640760B (zh) * | 2012-04-18 | 2014-02-26 | 联保作物科技有限公司 | 一种杀虫防病悬浮种衣剂 |
| JP6279563B2 (ja) | 2012-06-20 | 2018-02-14 | ビーエーエスエフ ソシエタス・ヨーロピアＢａｓｆ Ｓｅ | ピラゾール化合物およびピラゾール化合物を含む殺有害生物性混合物 |
| WO2014056780A1 (en) | 2012-10-12 | 2014-04-17 | Basf Se | A method for combating phytopathogenic harmful microbes on cultivated plants or plant propagation material |
| JP6576829B2 (ja) | 2012-12-20 | 2019-09-18 | ビーエーエスエフ アグロ ベー．ブイ． | トリアゾール化合物を含む組成物 |
| EP2783569A1 (en) | 2013-03-28 | 2014-10-01 | Basf Se | Compositions comprising a triazole compound |
| EP2835052A1 (en) | 2013-08-07 | 2015-02-11 | Basf Se | Fungicidal mixtures comprising pyrimidine fungicides |
| WO2015036059A1 (en) | 2013-09-16 | 2015-03-19 | Basf Se | Fungicidal pyrimidine compounds |
| CN105722833A (zh) | 2013-09-16 | 2016-06-29 | 巴斯夫欧洲公司 | 杀真菌的嘧啶化合物 |
| EP2979549A1 (en) | 2014-07-31 | 2016-02-03 | Basf Se | Method for improving the health of a plant |
| EP2910126A1 (en) | 2015-05-05 | 2015-08-26 | Bayer CropScience AG | Active compound combinations having insecticidal properties |
| CA2989253C (en) | 2015-07-02 | 2023-10-03 | BASF Agro B.V. | Pesticidal compositions comprising a triazole compound |
| KR20190036546A (ko) * | 2016-07-28 | 2019-04-04 | 메이오 파운데이션 포 메디칼 에쥬케이션 앤드 리써치 | 파킨 효소 기능의 소분자 활성화제 |
| EP4196464A4 (en) * | 2020-08-11 | 2024-12-25 | Board Of Trustees Of Michigan State University | PROTEASOMAL INHIBITORS AND THEIR USES |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3374241A (en) * | 1962-07-23 | 1968-03-19 | Du Pont | Diphenylcarbamyl derivatives of certain azoles |
| US3658813A (en) * | 1970-01-13 | 1972-04-25 | Janssen Pharmaceutica Nv | 1-(beta-aryl-beta-(r-oxy)-ethyl)-imidazoles |
| HU164653B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1971-07-23 | 1974-03-28 | ||
| GB1408877A (en) * | 1971-12-07 | 1975-10-08 | Boots Co Ltd | Substituted imidazoles and their use as pesticides |
-
1973
- 1973-06-21 GB GB2953573A patent/GB1469772A/en not_active Expired
-
1974
- 1974-06-11 CY CY995A patent/CY995A/xx unknown
- 1974-06-20 DD DD179314A patent/DD113164A5/xx unknown
- 1974-06-20 JP JP49070743A patent/JPS6010003B2/ja not_active Expired
- 1974-06-20 CS CS744365A patent/CS188185B2/cs unknown
- 1974-06-20 SU SU742045953A patent/SU585810A3/ru active
- 1974-06-20 DE DE2429523A patent/DE2429523A1/de active Granted
- 1974-06-21 FR FR7421739A patent/FR2234293B1/fr not_active Expired
- 1974-12-13 US US05/532,667 patent/US3991071A/en not_active Expired - Lifetime
- 1974-12-17 AU AU76526/74A patent/AU491880B2/en not_active Expired
- 1974-12-18 ZA ZA00748037A patent/ZA748037B/xx unknown
-
1977
- 1977-11-18 BE BE182736A patent/BE860966Q/xx not_active IP Right Cessation
-
1978
- 1978-02-21 US US05/879,564 patent/US4154945A/en not_active Expired - Lifetime
- 1978-12-31 MY MY1978125A patent/MY7800125A/xx unknown
-
1979
- 1979-03-17 KE KE2940A patent/KE2940A/xx unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU491880B2 (en) | 1976-06-17 |
| GB1469772A (en) | 1977-04-06 |
| SU585810A3 (ru) | 1977-12-25 |
| DE2429523C2 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1988-07-21 |
| CS188185B2 (en) | 1979-02-28 |
| US3991071A (en) | 1976-11-09 |
| DE2429523A1 (de) | 1975-01-16 |
| US4154945A (en) | 1979-05-15 |
| AU7652674A (en) | 1976-06-17 |
| KE2940A (en) | 1979-03-30 |
| FR2234293B1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1977-10-14 |
| MY7800125A (en) | 1978-12-31 |
| BE860966Q (fr) | 1978-05-18 |
| DD113164A5 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1975-05-20 |
| CY995A (en) | 1979-08-02 |
| FR2234293A1 (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1975-01-17 |
| JPS5031047A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1975-03-27 |
| ZA748037B (en) | 1976-01-28 |
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