CA1093085A - Diphenyl-triazolyl-methanes - Google Patents
Diphenyl-triazolyl-methanesInfo
- Publication number
- CA1093085A CA1093085A CA281,120A CA281120A CA1093085A CA 1093085 A CA1093085 A CA 1093085A CA 281120 A CA281120 A CA 281120A CA 1093085 A CA1093085 A CA 1093085A
- Authority
- CA
- Canada
- Prior art keywords
- triazol
- phenyl
- dimethyl
- butan
- propane
- 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
- JCFCCMVWFCHPFT-UHFFFAOYSA-N 4-benzhydryl-2h-triazole Chemical class N1N=NC(C(C=2C=CC=CC=2)C=2C=CC=CC=2)=C1 JCFCCMVWFCHPFT-UHFFFAOYSA-N 0.000 title abstract description 5
- 150000003839 salts Chemical class 0.000 claims abstract description 20
- 150000001875 compounds Chemical class 0.000 claims description 79
- 239000000460 chlorine Substances 0.000 claims description 12
- 241000244206 Nematoda Species 0.000 claims description 11
- 241000233866 Fungi Species 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 9
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 125000001309 chloro group Chemical group Cl* 0.000 claims description 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical group [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 1
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 1
- 239000001257 hydrogen Chemical group 0.000 claims 1
- 229910052739 hydrogen Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 abstract description 9
- 229910052736 halogen Inorganic materials 0.000 abstract description 6
- 150000002367 halogens Chemical class 0.000 abstract description 6
- 125000003545 alkoxy group Chemical group 0.000 abstract description 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract description 3
- 125000004414 alkyl thio group Chemical group 0.000 abstract description 3
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract description 3
- 125000004093 cyano group Chemical group *C#N 0.000 abstract description 3
- 125000001188 haloalkyl group Chemical group 0.000 abstract description 3
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract description 3
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract description 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract description 3
- 230000000855 fungicidal effect Effects 0.000 abstract description 2
- 208000015181 infectious disease Diseases 0.000 description 26
- 241000196324 Embryophyta Species 0.000 description 24
- 239000001294 propane Substances 0.000 description 23
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- -1 azole radical Chemical class 0.000 description 15
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 14
- 239000000203 mixture Substances 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 11
- 239000002904 solvent Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 9
- 230000001681 protective effect Effects 0.000 description 9
- 241000209219 Hordeum Species 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 8
- 239000007788 liquid Substances 0.000 description 8
- 238000002360 preparation method Methods 0.000 description 8
- 239000002689 soil Substances 0.000 description 8
- 239000003085 diluting agent Substances 0.000 description 7
- 240000008067 Cucumis sativus Species 0.000 description 6
- 235000013339 cereals Nutrition 0.000 description 6
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 5
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 5
- 241000221785 Erysiphales Species 0.000 description 5
- 239000002253 acid Substances 0.000 description 5
- 125000002877 alkyl aryl group Chemical group 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 229920000151 polyglycol Polymers 0.000 description 5
- 239000010695 polyglycol Substances 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical class C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- 241000220225 Malus Species 0.000 description 4
- 238000007792 addition Methods 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- 235000008504 concentrate Nutrition 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 239000000417 fungicide Substances 0.000 description 4
- 230000001069 nematicidal effect Effects 0.000 description 4
- 239000005645 nematicide Substances 0.000 description 4
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 4
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 3
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 3
- 206010017533 Fungal infection Diseases 0.000 description 3
- 206010061217 Infestation Diseases 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 241000896242 Podosphaera Species 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 241000209140 Triticum Species 0.000 description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 230000006378 damage Effects 0.000 description 3
- 239000011737 fluorine Substances 0.000 description 3
- 229910052731 fluorine Inorganic materials 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000011081 inoculation Methods 0.000 description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 3
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 230000009885 systemic effect Effects 0.000 description 3
- 241000894006 Bacteria Species 0.000 description 2
- 235000009849 Cucumis sativus Nutrition 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000004606 Fillers/Extenders Substances 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 240000008415 Lactuca sativa Species 0.000 description 2
- 235000003228 Lactuca sativa Nutrition 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 235000014328 Schoenoplectus acutus var occidentalis Nutrition 0.000 description 2
- 244000136421 Scirpus acutus Species 0.000 description 2
- 235000014326 Scirpus californicus Nutrition 0.000 description 2
- 235000017913 Scirpus lacustris Nutrition 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 235000021016 apples Nutrition 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
- 230000000875 corresponding effect Effects 0.000 description 2
- 201000010099 disease Diseases 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 150000002170 ethers Chemical class 0.000 description 2
- DQYBDCGIPTYXML-UHFFFAOYSA-N ethoxyethane;hydrate Chemical compound O.CCOCC DQYBDCGIPTYXML-UHFFFAOYSA-N 0.000 description 2
- 208000024386 fungal infectious disease Diseases 0.000 description 2
- 230000002464 fungitoxic effect Effects 0.000 description 2
- 239000008187 granular material Substances 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- XTEGVFVZDVNBPF-UHFFFAOYSA-N naphthalene-1,5-disulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1S(O)(=O)=O XTEGVFVZDVNBPF-UHFFFAOYSA-N 0.000 description 2
- 239000006072 paste Substances 0.000 description 2
- 244000052769 pathogen Species 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 239000011814 protection agent Substances 0.000 description 2
- 238000010992 reflux Methods 0.000 description 2
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- NVVRUQLFOFFFHM-UHFFFAOYSA-N (1-chloro-2,2-dimethyl-1-phenylpropyl)benzene Chemical compound C=1C=CC=CC=1C(Cl)(C(C)(C)C)C1=CC=CC=C1 NVVRUQLFOFFFHM-UHFFFAOYSA-N 0.000 description 1
- QRPQUCKVEKUJHN-UHFFFAOYSA-N 1,1-diphenyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C(=O)CC)C1=CC=CC=C1 QRPQUCKVEKUJHN-UHFFFAOYSA-N 0.000 description 1
- WYOHYWPJVBRQBZ-UHFFFAOYSA-N 1,2,2-triphenyl-2-(1,2,4-triazol-1-yl)ethanone Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 WYOHYWPJVBRQBZ-UHFFFAOYSA-N 0.000 description 1
- JABDWQHLXLJLGK-UHFFFAOYSA-N 1,2,2-triphenyl-2-(1,2,4-triazol-4-yl)ethanone Chemical compound C=1C=CC=CC=1C(N1C=NN=C1)(C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 JABDWQHLXLJLGK-UHFFFAOYSA-N 0.000 description 1
- 125000001401 1,2,4-triazol-4-yl group Chemical group N=1N=C([H])N([*])C=1[H] 0.000 description 1
- LAYGQNCVSZGHFN-UHFFFAOYSA-N 1,2-diphenyl-2-(1,2,4-triazol-1-yl)-2-[3-(trifluoromethyl)phenyl]ethanone Chemical compound FC(F)(F)C1=CC=CC(C(C(=O)C=2C=CC=CC=2)(C=2C=CC=CC=2)N2N=CN=C2)=C1 LAYGQNCVSZGHFN-UHFFFAOYSA-N 0.000 description 1
- LARIFUCUBNATPO-UHFFFAOYSA-N 1,2-diphenyl-2-(4-phenylphenyl)-2-(1,2,4-triazol-1-yl)ethanone Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C=1C=CC(=CC=1)C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 LARIFUCUBNATPO-UHFFFAOYSA-N 0.000 description 1
- NOZOEDDOJOXNBR-UHFFFAOYSA-N 1-(1,1-diphenylpentyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(CCCC)C1=CC=CC=C1 NOZOEDDOJOXNBR-UHFFFAOYSA-N 0.000 description 1
- VYCGBPSRZUKTDJ-UHFFFAOYSA-N 1-(1,1-diphenylpropyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(CC)C1=CC=CC=C1 VYCGBPSRZUKTDJ-UHFFFAOYSA-N 0.000 description 1
- YBNQYIZRFAPVNM-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)propan-2-one Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(N1N=CN=C1)(C(=O)C)C1=CC=CC=C1 YBNQYIZRFAPVNM-UHFFFAOYSA-N 0.000 description 1
- HMZGJNJZURPZJO-UHFFFAOYSA-N 1-(2,4-dichlorophenyl)-3,3-dimethyl-1-phenyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(N1N=CN=C1)(C(=O)C(C)(C)C)C1=CC=CC=C1 HMZGJNJZURPZJO-UHFFFAOYSA-N 0.000 description 1
- DGJFJIOWAWGVRP-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)-3,3-dimethyl-1-phenyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound CC1=CC(C)=CC=C1C(C(=O)C(C)(C)C)(N1N=CN=C1)C1=CC=CC=C1 DGJFJIOWAWGVRP-UHFFFAOYSA-N 0.000 description 1
- JVRFOWGDVQLCHA-UHFFFAOYSA-N 1-(2,4-dimethylphenyl)-3-methyl-1-phenyl-1-(1,2,4-triazol-1-yl)pentan-2-one Chemical compound C=1C=C(C)C=C(C)C=1C(N1N=CN=C1)(C(=O)C(C)CC)C1=CC=CC=C1 JVRFOWGDVQLCHA-UHFFFAOYSA-N 0.000 description 1
- ZKMXZDJJRMFJHK-UHFFFAOYSA-N 1-(2-chlorophenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)hexan-2-one Chemical compound C=1C=CC=C(Cl)C=1C(N1N=CN=C1)(C(=O)CCCC)C1=CC=CC=C1 ZKMXZDJJRMFJHK-UHFFFAOYSA-N 0.000 description 1
- WETNDRFWPQTQJS-UHFFFAOYSA-N 1-(2-chlorophenyl)-3,3-dimethyl-1-phenyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C=1C=CC=C(Cl)C=1C(N1N=CN=C1)(C(=O)C(C)(C)C)C1=CC=CC=C1 WETNDRFWPQTQJS-UHFFFAOYSA-N 0.000 description 1
- MFTLAMROXPRJPU-UHFFFAOYSA-N 1-(2-methyl-1,1-diphenylbutyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C(C)CC)C1=CC=CC=C1 MFTLAMROXPRJPU-UHFFFAOYSA-N 0.000 description 1
- JRLLEDJEPNCVEX-UHFFFAOYSA-N 1-(2-methyl-1,1-diphenylpropyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C(C)C)C1=CC=CC=C1 JRLLEDJEPNCVEX-UHFFFAOYSA-N 0.000 description 1
- FZTPIJWGFQWZJG-UHFFFAOYSA-N 1-(2-methylphenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)propan-2-one Chemical compound C=1C=CC=C(C)C=1C(N1N=CN=C1)(C(=O)C)C1=CC=CC=C1 FZTPIJWGFQWZJG-UHFFFAOYSA-N 0.000 description 1
- ROXLXQGQMMIJEP-UHFFFAOYSA-N 1-(3,4-dimethylphenyl)-3,3-dimethyl-1-phenyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C1=C(C)C(C)=CC=C1C(C(=O)C(C)(C)C)(N1N=CN=C1)C1=CC=CC=C1 ROXLXQGQMMIJEP-UHFFFAOYSA-N 0.000 description 1
- YIKGGRJOIZASKJ-UHFFFAOYSA-N 1-(3-methylphenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)hexan-2-one Chemical compound C=1C=CC(C)=CC=1C(N1N=CN=C1)(C(=O)CCCC)C1=CC=CC=C1 YIKGGRJOIZASKJ-UHFFFAOYSA-N 0.000 description 1
- MNUNINMASYIXAA-UHFFFAOYSA-N 1-(3-methylphenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)pentan-2-one Chemical compound C=1C=CC(C)=CC=1C(N1N=CN=C1)(C(=O)CCC)C1=CC=CC=C1 MNUNINMASYIXAA-UHFFFAOYSA-N 0.000 description 1
- VVWAWRAUBRBPTD-UHFFFAOYSA-N 1-(4-chlorophenyl)-1-(4-fluorophenyl)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C=1C=C(Cl)C=CC=1C(N1N=CN=C1)(C(=O)C(C)(C)C)C1=CC=C(F)C=C1 VVWAWRAUBRBPTD-UHFFFAOYSA-N 0.000 description 1
- LFDRIVJSDLBLTP-UHFFFAOYSA-N 1-(4-chlorophenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)propan-2-one Chemical compound C=1C=C(Cl)C=CC=1C(N1N=CN=C1)(C(=O)C)C1=CC=CC=C1 LFDRIVJSDLBLTP-UHFFFAOYSA-N 0.000 description 1
- PRQIUQUSZKQDHQ-UHFFFAOYSA-N 1-(4-chlorophenyl)-1-phenyl-1-(1,2,4-triazol-4-yl)butan-2-one Chemical compound C=1C=C(Cl)C=CC=1C(N1C=NN=C1)(C(=O)CC)C1=CC=CC=C1 PRQIUQUSZKQDHQ-UHFFFAOYSA-N 0.000 description 1
- TYILFIXCXGSLFC-UHFFFAOYSA-N 1-(4-chlorophenyl)-1-phenyl-1-(1,2,4-triazol-4-yl)propan-2-one Chemical compound C=1C=C(Cl)C=CC=1C(N1C=NN=C1)(C(=O)C)C1=CC=CC=C1 TYILFIXCXGSLFC-UHFFFAOYSA-N 0.000 description 1
- ALNCZSKKLZMIND-UHFFFAOYSA-N 1-(4-chlorophenyl)-2,2-diphenyl-2-(1,2,4-triazol-1-yl)ethanone Chemical compound C1=CC(Cl)=CC=C1C(=O)C(N1N=CN=C1)(C=1C=CC=CC=1)C1=CC=CC=C1 ALNCZSKKLZMIND-UHFFFAOYSA-N 0.000 description 1
- BHVFQZBHJYRHHU-UHFFFAOYSA-N 1-(4-chlorophenyl)-2-(3-methylphenyl)-2-phenyl-2-(1,2,4-triazol-1-yl)ethanone Chemical compound CC1=CC=CC(C(C(=O)C=2C=CC(Cl)=CC=2)(C=2C=CC=CC=2)N2N=CN=C2)=C1 BHVFQZBHJYRHHU-UHFFFAOYSA-N 0.000 description 1
- PFKZVIPZCPISGH-UHFFFAOYSA-N 1-(4-chlorophenyl)-3-methyl-1-phenyl-1-(1,2,4-triazol-1-yl)pentan-2-one Chemical compound C=1C=C(Cl)C=CC=1C(N1N=CN=C1)(C(=O)C(C)CC)C1=CC=CC=C1 PFKZVIPZCPISGH-UHFFFAOYSA-N 0.000 description 1
- WBCKEPMGFJFYHO-UHFFFAOYSA-N 1-(4-fluorophenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(C(=O)CC)C1=CC=CC=C1 WBCKEPMGFJFYHO-UHFFFAOYSA-N 0.000 description 1
- AYVWRBUJIRBMTC-UHFFFAOYSA-N 1-(4-fluorophenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)hexan-2-one Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(C(=O)CCCC)C1=CC=CC=C1 AYVWRBUJIRBMTC-UHFFFAOYSA-N 0.000 description 1
- SHXHPTFKFBHQCO-UHFFFAOYSA-N 1-(4-fluorophenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)pentan-2-one Chemical compound FC1=CC=C(C=C1)C(C(CCC)=O)(N1N=CN=C1)C1=CC=CC=C1 SHXHPTFKFBHQCO-UHFFFAOYSA-N 0.000 description 1
- PHTKVAHIRPXMSG-UHFFFAOYSA-N 1-(4-fluorophenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)propan-2-one Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(C(=O)C)C1=CC=CC=C1 PHTKVAHIRPXMSG-UHFFFAOYSA-N 0.000 description 1
- UGCTWJMQIGYPML-UHFFFAOYSA-N 1-(4-fluorophenyl)-3,3-dimethyl-1-phenyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(C(=O)C(C)(C)C)C1=CC=CC=C1 UGCTWJMQIGYPML-UHFFFAOYSA-N 0.000 description 1
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- ZZUFCTLCJUWOSV-UHFFFAOYSA-N furosemide Chemical class C1=C(Cl)C(S(=O)(=O)N)=CC(C(O)=O)=C1NCC1=CC=CO1 ZZUFCTLCJUWOSV-UHFFFAOYSA-N 0.000 description 1
- 230000035784 germination Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000003102 growth factor Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000012433 hydrogen halide Substances 0.000 description 1
- 229910000039 hydrogen halide Inorganic materials 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229960000448 lactic acid Drugs 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 150000002689 maleic acids Chemical class 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 229940043265 methyl isobutyl ketone Drugs 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 230000003071 parasitic effect Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 239000011148 porous material Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 208000029561 pustule Diseases 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004334 sorbic acid Substances 0.000 description 1
- 235000010199 sorbic acid Nutrition 0.000 description 1
- 229940075582 sorbic acid Drugs 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- 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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2628152A DE2628152C2 (de) | 1976-06-23 | 1976-06-23 | Fungizide und nematizide Mittel |
| DEP2628152.7 | 1976-06-23 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA1093085A true CA1093085A (en) | 1981-01-06 |
Family
ID=5981242
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA281,120A Expired CA1093085A (en) | 1976-06-23 | 1977-06-22 | Diphenyl-triazolyl-methanes |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US4140782A (en, 2012) |
| JP (1) | JPS52156928A (en, 2012) |
| AT (1) | AT354808B (en, 2012) |
| AU (1) | AU507606B2 (en, 2012) |
| BE (1) | BE855987A (en, 2012) |
| BR (1) | BR7704038A (en, 2012) |
| CA (1) | CA1093085A (en, 2012) |
| CH (1) | CH625677A5 (en, 2012) |
| CS (1) | CS192485B2 (en, 2012) |
| DD (1) | DD131991A5 (en, 2012) |
| DE (1) | DE2628152C2 (en, 2012) |
| DK (1) | DK143993C (en, 2012) |
| EG (1) | EG12727A (en, 2012) |
| FR (1) | FR2355452A1 (en, 2012) |
| GB (1) | GB1528564A (en, 2012) |
| HU (1) | HU176918B (en, 2012) |
| IL (1) | IL52345A (en, 2012) |
| IT (1) | IT1080208B (en, 2012) |
| NL (1) | NL7706778A (en, 2012) |
| PL (1) | PL107047B1 (en, 2012) |
| PT (1) | PT66683B (en, 2012) |
| SE (1) | SE7707231L (en, 2012) |
| SU (1) | SU663262A3 (en, 2012) |
| TR (1) | TR19281A (en, 2012) |
| ZA (1) | ZA773736B (en, 2012) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0194064A3 (en) * | 1985-03-06 | 1988-11-17 | Imperial Chemical Industries Plc | Azolyl substituted aralkyl compounds |
| US4978672A (en) * | 1986-03-07 | 1990-12-18 | Ciba-Geigy Corporation | Alpha-heterocyclc substituted tolunitriles |
| US4749713A (en) * | 1986-03-07 | 1988-06-07 | Ciba-Geigy Corporation | Alpha-heterocycle substituted tolunitriles |
| US4937250A (en) * | 1988-03-07 | 1990-06-26 | Ciba-Geigy Corporation | Alpha-heterocycle substituted tolunitriles |
| GB8716650D0 (en) * | 1987-07-15 | 1987-08-19 | Ici Plc | Use of olefinic compounds |
| TW533205B (en) | 1996-06-25 | 2003-05-21 | Novartis Ag | Substituted 3,5-diphenyl-l,2,4-triazoles and their pharmaceutical composition |
| RU2363157C1 (ru) * | 2008-03-24 | 2009-08-10 | Федеральное государственное образовательное учреждение высшего профессионального образования "Горский государственный аграрный университет" | Способ защиты зерна от болезней при хранении |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2037610A1 (de) | 1970-07-29 | 1972-02-03 | Bayer Ag | Neue alpha-substituierte Benzyl-azole, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
-
1976
- 1976-06-23 DE DE2628152A patent/DE2628152C2/de not_active Expired
-
1977
- 1977-06-15 US US05/806,889 patent/US4140782A/en not_active Expired - Lifetime
- 1977-06-16 CS CS773988A patent/CS192485B2/cs unknown
- 1977-06-17 PT PT66683A patent/PT66683B/pt unknown
- 1977-06-20 IL IL52345A patent/IL52345A/xx unknown
- 1977-06-20 NL NL7706778A patent/NL7706778A/xx not_active Application Discontinuation
- 1977-06-20 GB GB25653/77A patent/GB1528564A/en not_active Expired
- 1977-06-21 SU SU772497841A patent/SU663262A3/ru active
- 1977-06-21 PL PL1977199031A patent/PL107047B1/pl unknown
- 1977-06-21 DD DD7700199615A patent/DD131991A5/xx unknown
- 1977-06-21 IT IT24913/77A patent/IT1080208B/it active
- 1977-06-21 CH CH761677A patent/CH625677A5/de not_active IP Right Cessation
- 1977-06-22 AU AU26324/77A patent/AU507606B2/en not_active Expired
- 1977-06-22 ZA ZA00773736A patent/ZA773736B/xx unknown
- 1977-06-22 BR BR7704038A patent/BR7704038A/pt unknown
- 1977-06-22 TR TR19281A patent/TR19281A/xx unknown
- 1977-06-22 FR FR7719114A patent/FR2355452A1/fr active Granted
- 1977-06-22 EG EG367/77A patent/EG12727A/xx active
- 1977-06-22 DK DK275477A patent/DK143993C/da active
- 1977-06-22 SE SE7707231A patent/SE7707231L/xx not_active Application Discontinuation
- 1977-06-22 BE BE178677A patent/BE855987A/xx not_active IP Right Cessation
- 1977-06-22 CA CA281,120A patent/CA1093085A/en not_active Expired
- 1977-06-23 HU HU77BA3546A patent/HU176918B/hu unknown
- 1977-06-23 JP JP7395277A patent/JPS52156928A/ja active Granted
- 1977-06-23 AT AT443277A patent/AT354808B/de not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| DE2628152C2 (de) | 1985-03-28 |
| SU663262A3 (ru) | 1979-05-15 |
| DD131991A5 (de) | 1978-08-16 |
| DK143993C (da) | 1982-04-19 |
| US4140782A (en) | 1979-02-20 |
| IL52345A (en) | 1979-10-31 |
| ATA443277A (de) | 1979-06-15 |
| NL7706778A (nl) | 1977-12-28 |
| PT66683A (de) | 1977-07-01 |
| PT66683B (de) | 1978-11-17 |
| BR7704038A (pt) | 1978-07-04 |
| FR2355452A1 (fr) | 1978-01-20 |
| IL52345A0 (en) | 1977-08-31 |
| JPS6139921B2 (en, 2012) | 1986-09-06 |
| DE2628152A1 (de) | 1978-01-05 |
| BE855987A (fr) | 1977-12-22 |
| AT354808B (de) | 1979-01-25 |
| FR2355452B1 (en, 2012) | 1981-02-27 |
| SE7707231L (sv) | 1977-12-24 |
| IT1080208B (it) | 1985-05-16 |
| GB1528564A (en) | 1978-10-11 |
| CS192485B2 (en) | 1979-08-31 |
| EG12727A (en) | 1979-12-31 |
| ZA773736B (en) | 1978-05-30 |
| DK275477A (da) | 1977-12-24 |
| HU176918B (hu) | 1981-06-28 |
| TR19281A (tr) | 1978-10-27 |
| PL199031A1 (pl) | 1978-02-27 |
| AU2632477A (en) | 1979-01-04 |
| PL107047B1 (pl) | 1980-01-31 |
| DK143993B (da) | 1981-11-16 |
| JPS52156928A (en) | 1977-12-27 |
| CH625677A5 (en, 2012) | 1981-10-15 |
| AU507606B2 (en) | 1980-02-21 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MKEX | Expiry |