NO843191L - Azolyl-propannitriler, fremgangsmaate for fremstilling av disse, samt biocide midler inneholdende disse - Google Patents
Azolyl-propannitriler, fremgangsmaate for fremstilling av disse, samt biocide midler inneholdende disseInfo
- Publication number
- NO843191L NO843191L NO843191A NO843191A NO843191L NO 843191 L NO843191 L NO 843191L NO 843191 A NO843191 A NO 843191A NO 843191 A NO843191 A NO 843191A NO 843191 L NO843191 L NO 843191L
- Authority
- NO
- Norway
- Prior art keywords
- propanenitrile
- cyclohexyloxy
- imidazol
- triazol
- cyclopentyloxy
- Prior art date
Links
- 239000003139 biocide Substances 0.000 title claims abstract description 8
- 238000000034 method Methods 0.000 title claims abstract description 6
- -1 AZOLYL Chemical class 0.000 title claims description 84
- 150000001875 compounds Chemical class 0.000 claims abstract description 29
- 230000000855 fungicidal effect Effects 0.000 claims abstract description 12
- 150000003839 salts Chemical class 0.000 claims abstract description 10
- 230000000844 anti-bacterial effect Effects 0.000 claims abstract description 6
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 6
- 150000002367 halogens Chemical class 0.000 claims abstract description 6
- 150000007524 organic acids Chemical class 0.000 claims abstract description 4
- 235000005985 organic acids Nutrition 0.000 claims abstract description 4
- 125000004093 cyano group Chemical group *C#N 0.000 claims abstract description 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims abstract description 3
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims abstract 2
- 239000000203 mixture Substances 0.000 claims description 16
- 239000002253 acid Substances 0.000 claims description 11
- 230000012010 growth Effects 0.000 claims description 7
- IRYPOFDOUXGQHJ-UHFFFAOYSA-N 2-cyclopentyloxy-3-imidazol-1-yl-2-(2-methylphenyl)propanenitrile Chemical compound CC1=CC=CC=C1C(C#N)(OC1CCCC1)CN1C=NC=C1 IRYPOFDOUXGQHJ-UHFFFAOYSA-N 0.000 claims description 4
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 claims description 4
- 239000002904 solvent Substances 0.000 claims description 4
- QHRHELQUBVEMRB-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-cyclopentyloxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C1=CC(Cl)=CC=C1C(C#N)(OC1CCCC1)CN1N=CN=C1 QHRHELQUBVEMRB-UHFFFAOYSA-N 0.000 claims description 3
- WKKGMTQYGQGEFE-UHFFFAOYSA-N 2-cyclopentyloxy-2-phenyl-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C1CCCC1OC(C=1C=CC=CC=1)(C#N)CN1C=NC=N1 WKKGMTQYGQGEFE-UHFFFAOYSA-N 0.000 claims description 3
- DOVMAJKAYPJHEZ-UHFFFAOYSA-N 2-cyclopentyloxy-3-imidazol-1-yl-2-phenylpropanenitrile Chemical compound C1CCCC1OC(C=1C=CC=CC=1)(C#N)CN1C=CN=C1 DOVMAJKAYPJHEZ-UHFFFAOYSA-N 0.000 claims description 3
- 125000005279 aryl sulfonyloxy group Chemical group 0.000 claims description 3
- 239000002585 base Substances 0.000 claims description 3
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 3
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims description 2
- VFRKKPXBVORPBL-UHFFFAOYSA-N 2-(2-chlorophenyl)-2-cyclopentyloxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound ClC1=CC=CC=C1C(C#N)(OC1CCCC1)CN1N=CN=C1 VFRKKPXBVORPBL-UHFFFAOYSA-N 0.000 claims description 2
- GHKYRMKPFBHIDF-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-cyclopentyloxy-3-imidazol-1-ylpropanenitrile Chemical compound C1=CC(Cl)=CC=C1C(C#N)(OC1CCCC1)CN1C=NC=C1 GHKYRMKPFBHIDF-UHFFFAOYSA-N 0.000 claims description 2
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000006304 2-iodophenyl group Chemical group [H]C1=C([H])C(I)=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 claims description 2
- 125000005809 3,4,5-trimethoxyphenyl group Chemical group [H]C1=C(OC([H])([H])[H])C(OC([H])([H])[H])=C(OC([H])([H])[H])C([H])=C1* 0.000 claims description 2
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims description 2
- 125000004207 3-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(OC([H])([H])[H])=C1[H] 0.000 claims description 2
- 125000004860 4-ethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 125000004861 4-isopropyl phenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 2
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 claims description 2
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
- 125000004199 4-trifluoromethylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C(F)(F)F 0.000 claims description 2
- 150000001447 alkali salts Chemical class 0.000 claims description 2
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims description 2
- 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 claims 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 claims description 2
- 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 claims description 2
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 2
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 2
- 238000004519 manufacturing process Methods 0.000 claims description 2
- 150000007522 mineralic acids Chemical class 0.000 claims description 2
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims description 2
- 125000000636 p-nitrophenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)[N+]([O-])=O 0.000 claims description 2
- 230000001105 regulatory effect Effects 0.000 claims description 2
- VZXODZIJOKEODT-UHFFFAOYSA-N 2-cyclohexyloxy-2-(2,4-dichlorophenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound ClC1=CC(Cl)=CC=C1C(C#N)(OC1CCCCC1)CN1N=CN=C1 VZXODZIJOKEODT-UHFFFAOYSA-N 0.000 claims 2
- ZZDSACGVKRQZBZ-UHFFFAOYSA-N 2-cyclohexyloxy-2-(2-methylphenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound CC1=CC=CC=C1C(C#N)(OC1CCCCC1)CN1N=CN=C1 ZZDSACGVKRQZBZ-UHFFFAOYSA-N 0.000 claims 2
- FJUIDKNVJIEXNG-UHFFFAOYSA-N 2-cyclohexyloxy-3-imidazol-1-yl-2-(2-methylphenyl)propanenitrile Chemical compound CC1=CC=CC=C1C(C#N)(OC1CCCCC1)CN1C=NC=C1 FJUIDKNVJIEXNG-UHFFFAOYSA-N 0.000 claims 2
- XOYBZWGWWHRYAW-UHFFFAOYSA-N 2-cyclohexyloxy-3-imidazol-1-yl-2-phenylpropanenitrile Chemical compound C1CCCCC1OC(C=1C=CC=CC=1)(C#N)CN1C=CN=C1 XOYBZWGWWHRYAW-UHFFFAOYSA-N 0.000 claims 2
- BJYGWFYDGWRUKO-UHFFFAOYSA-N 2-cyclopentyloxy-2-(2-fluorophenyl)-3-imidazol-1-ylpropanenitrile Chemical compound FC1=CC=CC=C1C(C#N)(OC1CCCC1)CN1C=NC=C1 BJYGWFYDGWRUKO-UHFFFAOYSA-N 0.000 claims 2
- IGWAUAWEQAFDHJ-UHFFFAOYSA-N 2-(2-chlorophenyl)-2-cyclohexyloxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound ClC1=CC=CC=C1C(C#N)(OC1CCCCC1)CN1N=CN=C1 IGWAUAWEQAFDHJ-UHFFFAOYSA-N 0.000 claims 1
- PHABHKQSXLIAAO-UHFFFAOYSA-N 2-(2-chlorophenyl)-2-cyclohexyloxy-3-imidazol-1-ylpropanenitrile Chemical compound ClC1=CC=CC=C1C(C#N)(OC1CCCCC1)CN1C=NC=C1 PHABHKQSXLIAAO-UHFFFAOYSA-N 0.000 claims 1
- GYEYXKFWGAGUFV-UHFFFAOYSA-N 2-(2-chlorophenyl)-2-cyclopentyloxy-3-imidazol-1-ylpropanenitrile Chemical compound ClC1=CC=CC=C1C(C#N)(OC1CCCC1)CN1C=NC=C1 GYEYXKFWGAGUFV-UHFFFAOYSA-N 0.000 claims 1
- HHMWEJOTYVISGY-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-cyclohexyloxy-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C1=CC(Cl)=CC=C1C(C#N)(OC1CCCCC1)CN1N=CN=C1 HHMWEJOTYVISGY-UHFFFAOYSA-N 0.000 claims 1
- 125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 claims 1
- FKQJDEQWYRRXPS-UHFFFAOYSA-N 2-cyclohexyloxy-2-(2,4-dichlorophenyl)-3-imidazol-1-ylpropanenitrile Chemical compound ClC1=CC(Cl)=CC=C1C(C#N)(OC1CCCCC1)CN1C=NC=C1 FKQJDEQWYRRXPS-UHFFFAOYSA-N 0.000 claims 1
- AXKDKILWMBHXAU-UHFFFAOYSA-N 2-cyclohexyloxy-2-(2-fluorophenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound FC1=CC=CC=C1C(C#N)(OC1CCCCC1)CN1N=CN=C1 AXKDKILWMBHXAU-UHFFFAOYSA-N 0.000 claims 1
- OWGGEZMRQPJGMU-UHFFFAOYSA-N 2-cyclohexyloxy-2-(2-fluorophenyl)-3-imidazol-1-ylpropanenitrile Chemical compound FC1=CC=CC=C1C(C#N)(OC1CCCCC1)CN1C=NC=C1 OWGGEZMRQPJGMU-UHFFFAOYSA-N 0.000 claims 1
- XAINSPJNQBIIBK-UHFFFAOYSA-N 2-cyclohexyloxy-2-phenyl-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound C1CCCCC1OC(C=1C=CC=CC=1)(C#N)CN1C=NC=N1 XAINSPJNQBIIBK-UHFFFAOYSA-N 0.000 claims 1
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- XRVLFIAMMZWYJC-UHFFFAOYSA-N 2-cyclopentyloxy-2-(2-methylphenyl)-3-(1,2,4-triazol-1-yl)propanenitrile Chemical compound CC1=CC=CC=C1C(C#N)(OC1CCCC1)CN1N=CN=C1 XRVLFIAMMZWYJC-UHFFFAOYSA-N 0.000 claims 1
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- PBISAIGLBDRRSU-UHFFFAOYSA-N 2-cyclohexyloxy-2-(2-methylphenyl)-3-methylsulfonylpropanenitrile Chemical compound CC1=CC=CC=C1C(CS(C)(=O)=O)(C#N)OC1CCCCC1 PBISAIGLBDRRSU-UHFFFAOYSA-N 0.000 description 1
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- 241000228452 Venturia inaequalis Species 0.000 description 1
- 240000006365 Vitis vinifera Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
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- 150000007513 acids Chemical class 0.000 description 1
- 125000005037 alkyl phenyl group Chemical group 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- DNEHKUCSURWDGO-UHFFFAOYSA-N aluminum sodium Chemical compound [Na].[Al] DNEHKUCSURWDGO-UHFFFAOYSA-N 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 239000000010 aprotic solvent Substances 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 239000011324 bead Substances 0.000 description 1
- 150000008107 benzenesulfonic acids Chemical class 0.000 description 1
- 230000001588 bifunctional effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- RYAGRZNBULDMBW-UHFFFAOYSA-L calcium;3-(2-hydroxy-3-methoxyphenyl)-2-[2-methoxy-4-(3-sulfonatopropyl)phenoxy]propane-1-sulfonate Chemical compound [Ca+2].COC1=CC=CC(CC(CS([O-])(=O)=O)OC=2C(=CC(CCCS([O-])(=O)=O)=CC=2)OC)=C1O RYAGRZNBULDMBW-UHFFFAOYSA-L 0.000 description 1
- HCWYXKWQOMTBKY-UHFFFAOYSA-N calcium;dodecyl benzenesulfonate Chemical compound [Ca].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 HCWYXKWQOMTBKY-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical class OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 229910052570 clay Inorganic materials 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000009109 curative therapy Methods 0.000 description 1
- 230000018109 developmental process Effects 0.000 description 1
- 239000003085 diluting agent Substances 0.000 description 1
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- 230000001804 emulsifying effect Effects 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- BEFDCLMNVWHSGT-UHFFFAOYSA-N ethenylcyclopentane Chemical compound C=CC1CCCC1 BEFDCLMNVWHSGT-UHFFFAOYSA-N 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 125000001207 fluorophenyl group Chemical group 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 230000002068 genetic effect Effects 0.000 description 1
- 239000008187 granular material Substances 0.000 description 1
- 208000037824 growth disorder Diseases 0.000 description 1
- 238000003306 harvesting Methods 0.000 description 1
- GNOIPBMMFNIUFM-UHFFFAOYSA-N hexamethylphosphoric triamide Chemical compound CN(C)P(=O)(N(C)C)N(C)C GNOIPBMMFNIUFM-UHFFFAOYSA-N 0.000 description 1
- LELOWRISYMNNSU-UHFFFAOYSA-N hydrogen cyanide Chemical class N#C LELOWRISYMNNSU-UHFFFAOYSA-N 0.000 description 1
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 1
- 239000005457 ice water Substances 0.000 description 1
- 230000036512 infertility Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 230000009965 odorless effect Effects 0.000 description 1
- 210000000056 organ Anatomy 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 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
- 244000052769 pathogen Species 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 239000010773 plant oil Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- FVSKHRXBFJPNKK-UHFFFAOYSA-N propionitrile Chemical class CCC#N FVSKHRXBFJPNKK-UHFFFAOYSA-N 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 230000026267 regulation of growth Effects 0.000 description 1
- 230000005070 ripening Effects 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 230000007226 seed germination Effects 0.000 description 1
- 239000000741 silica gel Substances 0.000 description 1
- 229910002027 silica gel Inorganic materials 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000002689 soil Substances 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
- 238000010186 staining Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000036435 stunted growth Effects 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 150000003458 sulfonic acid derivatives Chemical class 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- 230000009105 vegetative growth Effects 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 239000000080 wetting agent 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3329213A DE3329213A1 (de) | 1983-08-10 | 1983-08-10 | Azolyl-propannitrile, verfahren zur herstellung dieser verbindungen sowie diese enthaltende biozide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO843191L true NO843191L (no) | 1985-02-11 |
Family
ID=6206443
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO843191A NO843191L (no) | 1983-08-10 | 1984-08-09 | Azolyl-propannitriler, fremgangsmaate for fremstilling av disse, samt biocide midler inneholdende disse |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US4594095A (fi) |
| EP (1) | EP0134515A1 (fi) |
| JP (1) | JPS6069068A (fi) |
| AU (1) | AU3181884A (fi) |
| BR (1) | BR8403995A (fi) |
| CS (1) | CS247085B2 (fi) |
| DD (1) | DD223349A5 (fi) |
| DE (1) | DE3329213A1 (fi) |
| DK (1) | DK380784A (fi) |
| ES (1) | ES8504153A1 (fi) |
| FI (1) | FI843165A (fi) |
| GR (1) | GR80062B (fi) |
| HU (1) | HUT34668A (fi) |
| IL (1) | IL72625A0 (fi) |
| NO (1) | NO843191L (fi) |
| PH (1) | PH24036A (fi) |
| PL (1) | PL138121B1 (fi) |
| PT (1) | PT79047B (fi) |
| RO (1) | RO89366A (fi) |
| YU (1) | YU133284A (fi) |
| ZA (1) | ZA846247B (fi) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3835742A1 (de) * | 1988-10-20 | 1990-05-10 | Lentia Gmbh | Neue nitroalkylazole |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| SE7600674L (sv) * | 1975-02-05 | 1976-08-06 | Rohm & Haas | Fungicider |
| US4073921A (en) * | 1975-03-12 | 1978-02-14 | Rohm And Haas Company | Substituted arylcyanoalkyl and diarylcyanoalkylimidazoles and fungical compositions and methods utilizing them |
| GB1553907A (en) * | 1976-07-29 | 1979-10-10 | Ici Ltd | Substituted ketones and their use as fungicidal compounds |
| US4366165A (en) * | 1977-05-19 | 1982-12-28 | Rohm And Haas Company | 1 and 4-Arylcyanoalkyl-1,2,4-triazoles and fungicidal use |
| NL189408C (nl) * | 1977-05-19 | 1993-04-01 | Rohm & Haas | 1,2,4-triazoolderivaten, fungicide preparaat en werkwijze voor het bestrijden van fytopathogene fungi. |
| AU8314482A (en) * | 1981-05-19 | 1982-11-25 | Imperial Chemical Industries Plc | 3-triazolyl(imidazolyl)-2,2 bis phenyl-propionamides |
| DE3125780A1 (de) * | 1981-06-30 | 1983-01-13 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | Imidazolyl-propionitrile, verfahren zur herstellung dieser verbindungen sowie diese enthaltende biozide mittel |
-
1983
- 1983-08-10 DE DE3329213A patent/DE3329213A1/de not_active Withdrawn
-
1984
- 1984-07-17 EP EP84108384A patent/EP0134515A1/de not_active Withdrawn
- 1984-07-30 YU YU01332/84A patent/YU133284A/xx unknown
- 1984-08-06 CS CS845945A patent/CS247085B2/cs unknown
- 1984-08-07 DK DK380784A patent/DK380784A/da not_active Application Discontinuation
- 1984-08-08 GR GR80062A patent/GR80062B/el unknown
- 1984-08-08 RO RO84115454A patent/RO89366A/ro unknown
- 1984-08-09 ES ES535002A patent/ES8504153A1/es not_active Expired
- 1984-08-09 PL PL1984249121A patent/PL138121B1/pl unknown
- 1984-08-09 NO NO843191A patent/NO843191L/no unknown
- 1984-08-09 PT PT79047A patent/PT79047B/pt unknown
- 1984-08-09 HU HU843043A patent/HUT34668A/hu unknown
- 1984-08-09 IL IL72625A patent/IL72625A0/xx unknown
- 1984-08-09 DD DD84266130A patent/DD223349A5/de unknown
- 1984-08-09 BR BR8403995A patent/BR8403995A/pt unknown
- 1984-08-10 JP JP59166656A patent/JPS6069068A/ja active Granted
- 1984-08-10 AU AU31818/84A patent/AU3181884A/en not_active Abandoned
- 1984-08-10 US US06/640,156 patent/US4594095A/en not_active Expired - Fee Related
- 1984-08-10 ZA ZA846247A patent/ZA846247B/xx unknown
- 1984-08-10 PH PH31094A patent/PH24036A/en unknown
- 1984-08-10 FI FI843165A patent/FI843165A/fi not_active Application Discontinuation
Also Published As
| Publication number | Publication date |
|---|---|
| AU3181884A (en) | 1985-02-14 |
| GR80062B (en) | 1984-12-11 |
| DE3329213A1 (de) | 1985-02-21 |
| DK380784A (da) | 1985-02-11 |
| IL72625A0 (en) | 1984-11-30 |
| JPS6146475B2 (fi) | 1986-10-14 |
| CS247085B2 (en) | 1986-11-13 |
| ES535002A0 (es) | 1985-04-16 |
| PT79047A (de) | 1984-09-01 |
| PL138121B1 (en) | 1986-08-30 |
| RO89366A (ro) | 1986-05-30 |
| PH24036A (en) | 1990-02-09 |
| EP0134515A1 (de) | 1985-03-20 |
| PL249121A1 (en) | 1985-04-24 |
| FI843165A0 (fi) | 1984-08-10 |
| FI843165A (fi) | 1985-02-11 |
| PT79047B (de) | 1986-08-12 |
| DK380784D0 (da) | 1984-08-07 |
| YU133284A (en) | 1986-06-30 |
| DD223349A5 (de) | 1985-06-12 |
| US4594095A (en) | 1986-06-10 |
| BR8403995A (pt) | 1985-07-16 |
| HUT34668A (en) | 1985-04-28 |
| ZA846247B (en) | 1985-03-27 |
| ES8504153A1 (es) | 1985-04-16 |
| JPS6069068A (ja) | 1985-04-19 |
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