HU176918B - Fungicidnye i nematocidnye kompozicii dlja zahhity rastenijj - Google Patents
Fungicidnye i nematocidnye kompozicii dlja zahhity rastenijj Download PDFInfo
- Publication number
- HU176918B HU176918B HU77BA3546A HUBA003546A HU176918B HU 176918 B HU176918 B HU 176918B HU 77BA3546 A HU77BA3546 A HU 77BA3546A HU BA003546 A HUBA003546 A HU BA003546A HU 176918 B HU176918 B HU 176918B
- Authority
- HU
- Hungary
- Prior art keywords
- triazol
- phenyl
- diphenyl
- chlorophenyl
- weight
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title claims description 11
- 230000001069 nematicidal effect Effects 0.000 title claims description 8
- 239000000417 fungicide Substances 0.000 title abstract description 3
- 239000005645 nematicide Substances 0.000 title abstract description 3
- 239000000203 mixture Substances 0.000 title description 41
- 230000001681 protective effect Effects 0.000 title description 7
- 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 claims abstract description 8
- 239000004480 active ingredient Substances 0.000 claims description 48
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 19
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 claims description 14
- 239000002904 solvent Substances 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N silicon dioxide Inorganic materials O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 11
- 150000003839 salts Chemical class 0.000 claims description 7
- 229920000151 polyglycol Polymers 0.000 claims description 6
- 239000010695 polyglycol Substances 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 4
- 239000007787 solid Substances 0.000 claims description 4
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000000969 carrier Substances 0.000 claims description 3
- 235000013312 flour Nutrition 0.000 claims description 3
- 239000007788 liquid Substances 0.000 claims description 3
- 239000003208 petroleum Substances 0.000 claims description 3
- 239000008096 xylene Substances 0.000 claims description 3
- 125000004448 alkyl carbonyl group Chemical group 0.000 claims description 2
- 239000004476 plant protection product Substances 0.000 claims description 2
- 239000010453 quartz Substances 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 1
- 229920001732 Lignosulfonate Polymers 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 150000001875 compounds Chemical class 0.000 abstract description 23
- 241000196324 Embryophyta Species 0.000 description 21
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- -1 diphenyltriazolyl Chemical group 0.000 description 14
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 13
- 239000003995 emulsifying agent Substances 0.000 description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 208000015181 infectious disease Diseases 0.000 description 9
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 7
- 238000009472 formulation Methods 0.000 description 7
- 239000001294 propane Substances 0.000 description 7
- 239000002689 soil Substances 0.000 description 7
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 6
- 241000221785 Erysiphales Species 0.000 description 6
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 6
- 240000005979 Hordeum vulgare Species 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- 239000004615 ingredient Substances 0.000 description 6
- 238000002360 preparation method Methods 0.000 description 6
- 239000000243 solution Substances 0.000 description 6
- 241000233866 Fungi Species 0.000 description 5
- 235000013339 cereals Nutrition 0.000 description 5
- 239000012141 concentrate Substances 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000007921 spray Substances 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- ZKJIRAVFIKVYNF-UHFFFAOYSA-N 1-(2,2-dimethyl-1,1-diphenylpropyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C(C)(C)C)C1=CC=CC=C1 ZKJIRAVFIKVYNF-UHFFFAOYSA-N 0.000 description 4
- 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 4
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 4
- 235000007340 Hordeum vulgare Nutrition 0.000 description 4
- 241000244206 Nematoda Species 0.000 description 4
- 239000001273 butane Substances 0.000 description 4
- 239000003814 drug Substances 0.000 description 4
- 229940079593 drug Drugs 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 235000011389 fruit/vegetable juice Nutrition 0.000 description 4
- 239000008187 granular material Substances 0.000 description 4
- 235000012054 meals Nutrition 0.000 description 4
- 239000004575 stone Substances 0.000 description 4
- 239000000725 suspension Substances 0.000 description 4
- 230000009885 systemic effect Effects 0.000 description 4
- 125000003626 1,2,4-triazol-1-yl group Chemical group [*]N1N=C([H])N=C1[H] 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-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
- 241000221787 Erysiphe Species 0.000 description 3
- 206010017533 Fungal infection Diseases 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 150000007513 acids Chemical class 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- 238000011835 investigation 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
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 3
- 238000005507 spraying Methods 0.000 description 3
- BSPCZKHHFNNQPA-UHFFFAOYSA-N 1,1-diphenyl-1-(1,2,4-triazol-1-yl)propan-2-one Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C(=O)C)C1=CC=CC=C1 BSPCZKHHFNNQPA-UHFFFAOYSA-N 0.000 description 2
- IWEVCLOTVZBYLY-UHFFFAOYSA-N 1,1-diphenyl-1-(1,2,4-triazol-4-yl)butan-2-one Chemical compound C=1C=CC=CC=1C(N1C=NN=C1)(C(=O)CC)C1=CC=CC=C1 IWEVCLOTVZBYLY-UHFFFAOYSA-N 0.000 description 2
- IQXZABPATZUJOG-UHFFFAOYSA-N 1,1-diphenyl-1-(1,2,4-triazol-4-yl)propan-2-one Chemical compound C=1C=CC=CC=1C(N1C=NN=C1)(C(=O)C)C1=CC=CC=C1 IQXZABPATZUJOG-UHFFFAOYSA-N 0.000 description 2
- MDJYTLARTOAUBD-UHFFFAOYSA-N 1-(1,1-diphenylbutyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(CCC)C1=CC=CC=C1 MDJYTLARTOAUBD-UHFFFAOYSA-N 0.000 description 2
- DXNJVWYNJUYRMV-UHFFFAOYSA-N 1-(1,1-diphenylethyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C)C1=CC=CC=C1 DXNJVWYNJUYRMV-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 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 2
- 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 2
- 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 2
- PMASELDKLYDFIE-UHFFFAOYSA-N 1-[1-(4-chlorophenyl)-1-phenylbutyl]-1,2,4-triazole Chemical compound C=1C=C(Cl)C=CC=1C(N1N=CN=C1)(CCC)C1=CC=CC=C1 PMASELDKLYDFIE-UHFFFAOYSA-N 0.000 description 2
- UNXPHOXAADCKHK-UHFFFAOYSA-N 1-[1-(4-chlorophenyl)-2,2-dimethyl-1-phenylpropyl]-1,2,4-triazole Chemical compound C=1C=C(Cl)C=CC=1C(N1N=CN=C1)(C(C)(C)C)C1=CC=CC=C1 UNXPHOXAADCKHK-UHFFFAOYSA-N 0.000 description 2
- LIXWVBZELRVSDX-UHFFFAOYSA-N 1-[1-(4-fluorophenyl)-1-phenylbutyl]-1,2,4-triazole Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(CCC)C1=CC=CC=C1 LIXWVBZELRVSDX-UHFFFAOYSA-N 0.000 description 2
- GRTBXROGXPENFO-UHFFFAOYSA-N 1-[1-(4-fluorophenyl)-1-phenylethyl]-1,2,4-triazole Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(C)C1=CC=CC=C1 GRTBXROGXPENFO-UHFFFAOYSA-N 0.000 description 2
- DVEZDPJUGMJZMY-UHFFFAOYSA-N 1-[1-(4-fluorophenyl)-1-phenylpropyl]-1,2,4-triazole Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(CC)C1=CC=CC=C1 DVEZDPJUGMJZMY-UHFFFAOYSA-N 0.000 description 2
- RIEVXHFLPLTXKM-UHFFFAOYSA-N 1-[1-(4-fluorophenyl)-2,2-dimethyl-1-phenylpropyl]-1,2,4-triazole Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(C(C)(C)C)C1=CC=CC=C1 RIEVXHFLPLTXKM-UHFFFAOYSA-N 0.000 description 2
- AOAJNMPQRYRBRJ-UHFFFAOYSA-N 1-[1-(4-fluorophenyl)-2-methyl-1-phenylbutyl]-1,2,4-triazole Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(C(C)CC)C1=CC=CC=C1 AOAJNMPQRYRBRJ-UHFFFAOYSA-N 0.000 description 2
- WUIPXBDZTBQMKO-UHFFFAOYSA-N 3,3-dimethyl-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)C(C)(C)C)C1=CC=CC=C1 WUIPXBDZTBQMKO-UHFFFAOYSA-N 0.000 description 2
- ONAFLWKBJXJBTR-UHFFFAOYSA-N 4-(1,1-diphenylethyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1C=NN=C1)(C)C1=CC=CC=C1 ONAFLWKBJXJBTR-UHFFFAOYSA-N 0.000 description 2
- GIFBTTYIMQEKDE-UHFFFAOYSA-N 4-(1,1-diphenylpropyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1C=NN=C1)(CC)C1=CC=CC=C1 GIFBTTYIMQEKDE-UHFFFAOYSA-N 0.000 description 2
- QNFQIJFBPNOOFA-UHFFFAOYSA-N 4-[1-(4-chlorophenyl)-1-phenylethyl]-1,2,4-triazole Chemical compound C=1C=C(Cl)C=CC=1C(N1C=NN=C1)(C)C1=CC=CC=C1 QNFQIJFBPNOOFA-UHFFFAOYSA-N 0.000 description 2
- FHUDTCABWGCSRD-UHFFFAOYSA-N 4-[1-(4-chlorophenyl)-1-phenylpropyl]-1,2,4-triazole Chemical compound C=1C=C(Cl)C=CC=1C(N1C=NN=C1)(CC)C1=CC=CC=C1 FHUDTCABWGCSRD-UHFFFAOYSA-N 0.000 description 2
- CBPCQSVRIYRCJK-UHFFFAOYSA-N 4-[1-(4-chlorophenyl)-2,2-dimethylpropyl]-1,2,4-triazole Chemical compound ClC1=CC=C(C=C1)C(C(C)(C)C)N1C=NN=C1 CBPCQSVRIYRCJK-UHFFFAOYSA-N 0.000 description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 2
- 241000894006 Bacteria Species 0.000 description 2
- 240000008067 Cucumis sativus Species 0.000 description 2
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 244000141359 Malus pumila Species 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 2
- JXLHNMVSKXFWAO-UHFFFAOYSA-N azane;7-fluoro-2,1,3-benzoxadiazole-4-sulfonic acid Chemical compound N.OS(=O)(=O)C1=CC=C(F)C2=NON=C12 JXLHNMVSKXFWAO-UHFFFAOYSA-N 0.000 description 2
- 239000004305 biphenyl Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- 239000004927 clay Substances 0.000 description 2
- 238000011109 contamination Methods 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 208000024386 fungal infectious disease Diseases 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000003071 parasitic effect Effects 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000003389 potentiating effect Effects 0.000 description 2
- 239000011541 reaction mixture Substances 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 229910052938 sodium sulfate Inorganic materials 0.000 description 2
- 235000011152 sodium sulphate Nutrition 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000000454 talc Substances 0.000 description 2
- 229910052623 talc Inorganic materials 0.000 description 2
- 150000003852 triazoles Chemical class 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
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 description 1
- OLAZGRUFCKQPIW-UHFFFAOYSA-N 1,1-diphenyl-1-(1,2,4-triazol-1-yl)hexan-2-one Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C(=O)CCCC)C1=CC=CC=C1 OLAZGRUFCKQPIW-UHFFFAOYSA-N 0.000 description 1
- CRGNTSMNHXLDKO-UHFFFAOYSA-N 1,1-diphenyl-1-(1,2,4-triazol-1-yl)pentan-2-one Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C(=O)CCC)C1=CC=CC=C1 CRGNTSMNHXLDKO-UHFFFAOYSA-N 0.000 description 1
- SPNSHIZBPJVXRR-UHFFFAOYSA-N 1,1-diphenyl-1-(1,2,4-triazol-4-yl)pentan-2-one Chemical compound C=1C=CC=CC=1C(N1C=NN=C1)(C(=O)CCC)C1=CC=CC=C1 SPNSHIZBPJVXRR-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
- VPGSXIKVUASQIY-UHFFFAOYSA-N 1,2-dibutylnaphthalene Chemical compound C1=CC=CC2=C(CCCC)C(CCCC)=CC=C21 VPGSXIKVUASQIY-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
- YSLPZXWCBWFYKH-UHFFFAOYSA-N 1-(2-chlorophenyl)-3,3-dimethyl-1-phenyl-1-(1,2,4-triazol-4-yl)butan-2-one Chemical compound C=1C=CC=C(Cl)C=1C(N1C=NN=C1)(C(=O)C(C)(C)C)C1=CC=CC=C1 YSLPZXWCBWFYKH-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
- 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
- ZQSICTDKLZCDFF-UHFFFAOYSA-N 1-(4-chlorophenyl)-1-phenyl-1-(1,2,4-triazol-1-yl)butan-2-one Chemical compound C=1C=C(Cl)C=CC=1C(N1N=CN=C1)(C(=O)CC)C1=CC=CC=C1 ZQSICTDKLZCDFF-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
- UAOCFRPYROIFJO-UHFFFAOYSA-N 1-(4-chlorophenyl)-1-phenyl-1-(1,2,4-triazol-4-yl)pentan-2-one Chemical compound C=1C=C(Cl)C=CC=1C(N1C=NN=C1)(C(=O)CCC)C1=CC=CC=C1 UAOCFRPYROIFJO-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
- 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
- KHYIGEFJYYDNIM-UHFFFAOYSA-N 1-[1-(2-chlorophenyl)-1-phenylpentyl]-1,2,4-triazole Chemical compound C=1C=CC=C(Cl)C=1C(N1N=CN=C1)(CCCC)C1=CC=CC=C1 KHYIGEFJYYDNIM-UHFFFAOYSA-N 0.000 description 1
- BTIGNMAJFKINCI-UHFFFAOYSA-N 1-[1-(4-fluorophenyl)-1-phenylpentyl]-1,2,4-triazole Chemical compound C=1C=C(F)C=CC=1C(N1N=CN=C1)(CCCC)C1=CC=CC=C1 BTIGNMAJFKINCI-UHFFFAOYSA-N 0.000 description 1
- HAGYXNVNFOULKK-UHFFFAOYSA-N 1-trityl-1,2,4-triazole Chemical compound N1=CN=CN1C(C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 HAGYXNVNFOULKK-UHFFFAOYSA-N 0.000 description 1
- RSEODCKMQVVKDQ-UHFFFAOYSA-N 3,3-dimethyl-1,1-diphenyl-1-(1,2,4-triazol-4-yl)butan-2-one Chemical compound C=1C=CC=CC=1C(N1C=NN=C1)(C(=O)C(C)(C)C)C1=CC=CC=C1 RSEODCKMQVVKDQ-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- LFHXRJGCPDVCBI-UHFFFAOYSA-N 3-methyl-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)C(C)C)C1=CC=CC=C1 LFHXRJGCPDVCBI-UHFFFAOYSA-N 0.000 description 1
- IBMXEIKCXSPZJB-UHFFFAOYSA-N 3-methyl-1,1-diphenyl-1-(1,2,4-triazol-1-yl)pentan-2-one Chemical compound C=1C=CC=CC=1C(N1N=CN=C1)(C(=O)C(C)CC)C1=CC=CC=C1 IBMXEIKCXSPZJB-UHFFFAOYSA-N 0.000 description 1
- INXMRPXOWYVBNT-UHFFFAOYSA-N 4-(1,1-diphenylbutyl)-1,2,4-triazole Chemical compound C=1C=CC=CC=1C(N1C=NN=C1)(CCC)C1=CC=CC=C1 INXMRPXOWYVBNT-UHFFFAOYSA-N 0.000 description 1
- ZHDUOTGPZKVRHD-UHFFFAOYSA-N 4-[1-(4-chlorophenyl)-1-phenylbutyl]-1,2,4-triazole Chemical compound C=1C=C(Cl)C=CC=1C(N1C=NN=C1)(CCC)C1=CC=CC=C1 ZHDUOTGPZKVRHD-UHFFFAOYSA-N 0.000 description 1
- 229920001817 Agar Polymers 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000294569 Aphelenchoides Species 0.000 description 1
- 241000235349 Ascomycota Species 0.000 description 1
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- 241000399949 Ditylenchus dipsaci Species 0.000 description 1
- 239000005909 Kieselgur Substances 0.000 description 1
- 240000008415 Lactuca sativa Species 0.000 description 1
- 235000003228 Lactuca sativa Nutrition 0.000 description 1
- 241001220360 Longidorus Species 0.000 description 1
- 241001143352 Meloidogyne Species 0.000 description 1
- 241000243786 Meloidogyne incognita Species 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- 241000282339 Mustela Species 0.000 description 1
- 208000031888 Mycoses Diseases 0.000 description 1
- 208000000291 Nematode infections Diseases 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- 241001503460 Plasmodiophorida Species 0.000 description 1
- 241000896242 Podosphaera Species 0.000 description 1
- 241000193943 Pratylenchus Species 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 239000006004 Quartz sand Substances 0.000 description 1
- 241000201375 Radopholus similis Species 0.000 description 1
- 241001220308 Trichodorus Species 0.000 description 1
- 235000021307 Triticum Nutrition 0.000 description 1
- 244000098338 Triticum aestivum Species 0.000 description 1
- 241001540447 Tylenchus Species 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical group ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- 241000201423 Xiphinema Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 239000008272 agar Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000001857 anti-mycotic effect Effects 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 239000002969 artificial stone Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 235000010290 biphenyl Nutrition 0.000 description 1
- 125000006267 biphenyl group Chemical group 0.000 description 1
- SMLHHBQGIJMAIM-UHFFFAOYSA-N calcium;2-dodecylbenzenesulfonic acid Chemical compound [Ca].CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O SMLHHBQGIJMAIM-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 210000003608 fece Anatomy 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 244000053095 fungal pathogen Species 0.000 description 1
- 231100000162 fungitoxic Toxicity 0.000 description 1
- 230000002464 fungitoxic effect Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 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
- 150000002576 ketones Chemical class 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 239000010871 livestock manure Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 244000052769 pathogen Species 0.000 description 1
- 239000003415 peat Substances 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N phenylbenzene Natural products C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229910052573 porcelain Inorganic materials 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- WSWCOQWTEOXDQX-MQQKCMAXSA-N sorbic acid group Chemical group C(\C=C\C=C\C)(=O)O WSWCOQWTEOXDQX-MQQKCMAXSA-N 0.000 description 1
- 239000012258 stirred mixture Substances 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- CYRMSUTZVYGINF-UHFFFAOYSA-N trichlorofluoromethane Chemical compound FC(Cl)(Cl)Cl CYRMSUTZVYGINF-UHFFFAOYSA-N 0.000 description 1
- 229940029284 trichlorofluoromethane Drugs 0.000 description 1
- 239000004563 wettable powder 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 (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE2628152A DE2628152C2 (de) | 1976-06-23 | 1976-06-23 | Fungizide und nematizide Mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU176918B true HU176918B (hu) | 1981-06-28 |
Family
ID=5981242
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU77BA3546A HU176918B (hu) | 1976-06-23 | 1977-06-23 | Fungicidnye i nematocidnye kompozicii dlja zahhity rastenijj |
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 |
| CA1093085A (en) | 1981-01-06 |
| 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 |
| 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 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EP0085333B1 (de) | Ether-Derivate von substituierten 1-Hydroxyalkyl-azolen, Verfahren zu ihrer Herstellung sowie ihre Verwendung als Fungizide und Pflanzenwachstumsregulatoren | |
| HU191671B (en) | Regulating increase and fungicide preparates consisting of -as reagent - 1-hydroxi-ethil-azol derivatives and process for producing of reagents | |
| JPS5953266B2 (ja) | トリアゾリル−アルカノンおよびこれらの塩の製造方法 | |
| JPS6128668B2 (en, 2012) | ||
| IE842345L (en) | 1-hydroxyethyltriazole derivatives | |
| DD208752A5 (de) | Pflanzenschutzmittel, verfahren zu ihrer herstellung sowie verwendung von substituierten 1--hydroxyalkyl-azolyl-derivaten | |
| JPS6222961B2 (en, 2012) | ||
| HU176366B (en) | Fungicide compositions containing bracket-1-pheny1-2-triazoly1-ethy1-bracket closed-ether derivatives as active agents and process for producing the active agents | |
| HU177167B (en) | Fungicide compositions and process for preparing 4-azolyl-4-phenoxy-butanoic acid derivatives as active substances thereof | |
| HU176919B (hu) | Fungicidnye preparaty soderzhahhie galogenozamehhjonnye proizvodnye 1-azolil-butana i sposob poluchenija aktivnykh vehhestv | |
| HU181644B (en) | Fungicide compositions containing oximino-triazolyl-ethane derivatives as active substances and process for preparing the active substances | |
| IL44821A (en) | Plant fungicidal and mircobicidal compositions containing certaining certain omega-imidazolyl-omega-phenoxy(or phenylthio)-alkanones | |
| US4505922A (en) | Triazolealkynol fungicidal agents | |
| DE2734365A1 (de) | Heterocyclische verbindungen, verfahren zu ihrer herstellung und diese verbindungen enthaltende fungizide zusammensetzungen | |
| HU176915B (hu) | Fungicidnye kompozicii soderzhahhie zamehhennye fenoksi-triazolil-butil-slozhnykh efirov,i sposob poluchenija aktivnykh agentov | |
| HU189189B (en) | Preparatives regulating the growth of plants, fungicides and inhibiting the growth of plants preparatives, containing as reagent azolile alcenols or oil-derivatives | |
| HU176918B (hu) | Fungicidnye i nematocidnye kompozicii dlja zahhity rastenijj | |
| JPH058161B2 (en, 2012) | ||
| DK172423B1 (da) | Triazolderivater, farmaceutiske og landbrugsmæssige fungicide præparater indeholdende disse og fremgangsmåde til behandling | |
| JPH0422913B2 (en, 2012) | ||
| HU176746B (en) | Fungicide compositions comtaining 1-bracket-2-halogeno-2-phenyl-ethyl-bracket closed-triasole derivatives as active agents and process for producing the active agents | |
| JPS6026111B2 (ja) | 新規な１−アゾリル−４−ヒドロキシ−ブタン誘導体，その製造方法およびそれを活性成分として含有する殺菌剤組成物 | |
| JPS599553B2 (ja) | 新規ハロゲントリアゾ−ル誘導体の製法 | |
| JPS58103368A (ja) | アゾリル−ペンテン誘導体、その製法および該誘導体を含有する殺生剤 | |
| HU176916B (hu) | Fungicidnye preparaty soderzhahhie slozhnye ehfiry imidazolil-fenoksi-alkogolja i sposob poluchenija aktivnykh vehhestv |