DE2602964A1 - Fungicides mittel - Google Patents
Fungicides mittelInfo
- Publication number
- DE2602964A1 DE2602964A1 DE19762602964 DE2602964A DE2602964A1 DE 2602964 A1 DE2602964 A1 DE 2602964A1 DE 19762602964 DE19762602964 DE 19762602964 DE 2602964 A DE2602964 A DE 2602964A DE 2602964 A1 DE2602964 A1 DE 2602964A1
- Authority
- DE
- Germany
- Prior art keywords
- methyl
- dimethyl
- hydrogen
- pyrazolium
- active ingredient
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Withdrawn
Links
- 239000000417 fungicide Substances 0.000 title claims description 18
- 239000003795 chemical substances by application Substances 0.000 title description 2
- -1 pyrazolium compound Chemical class 0.000 claims description 68
- 241000196324 Embryophyta Species 0.000 claims description 53
- 239000004480 active ingredient Substances 0.000 claims description 23
- 235000007340 Hordeum vulgare Nutrition 0.000 claims description 20
- 241000209140 Triticum Species 0.000 claims description 20
- 235000021307 Triticum Nutrition 0.000 claims description 20
- 239000000203 mixture Substances 0.000 claims description 19
- 125000001424 substituent group Chemical group 0.000 claims description 18
- 150000001875 compounds Chemical class 0.000 claims description 17
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 15
- 239000007921 spray Substances 0.000 claims description 15
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical group COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 claims description 14
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical group [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims description 13
- 239000001257 hydrogen Substances 0.000 claims description 13
- 150000001450 anions Chemical class 0.000 claims description 12
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical group I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims description 11
- 230000000855 fungicidal effect Effects 0.000 claims description 10
- 150000002431 hydrogen Chemical class 0.000 claims description 9
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 claims description 9
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical group OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 claims description 9
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 9
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 8
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- 239000000460 chlorine Substances 0.000 claims description 8
- 229910052731 fluorine Inorganic materials 0.000 claims description 8
- 239000011737 fluorine Substances 0.000 claims description 8
- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 7
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
- 229910002651 NO3 Chemical group 0.000 claims description 6
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical group [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 6
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical group [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 5
- 230000009194 climbing Effects 0.000 claims description 5
- 235000013399 edible fruits Nutrition 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical group [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 claims description 5
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 claims description 5
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical group CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims description 5
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- SRSXLGNVWSONIS-UHFFFAOYSA-M benzenesulfonate Chemical group [O-]S(=O)(=O)C1=CC=CC=C1 SRSXLGNVWSONIS-UHFFFAOYSA-M 0.000 claims description 4
- 235000013339 cereals Nutrition 0.000 claims description 4
- 150000002367 halogens Chemical class 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical group OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 4
- 239000007788 liquid Substances 0.000 claims description 4
- 239000002736 nonionic surfactant Substances 0.000 claims description 4
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical group [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 4
- 239000010452 phosphate Chemical group 0.000 claims description 4
- 241000221787 Erysiphe Species 0.000 claims description 3
- 229940077388 benzenesulfonate Drugs 0.000 claims description 3
- 229910052736 halogen Inorganic materials 0.000 claims description 3
- 241000317942 Venturia <ichneumonid wasp> Species 0.000 claims description 2
- 239000000969 carrier Substances 0.000 claims description 2
- 150000001805 chlorine compounds Chemical group 0.000 claims 3
- 240000005979 Hordeum vulgare Species 0.000 claims 1
- 241000233614 Phytophthora Species 0.000 claims 1
- 239000012876 carrier material Substances 0.000 claims 1
- 125000001501 propionyl group Chemical group O=C([*])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 229910021653 sulphate ion Inorganic materials 0.000 claims 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-M toluene-4-sulfonate Chemical group CC1=CC=C(S([O-])(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-M 0.000 claims 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical class C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 description 31
- 241000220225 Malus Species 0.000 description 28
- 235000011430 Malus pumila Nutrition 0.000 description 26
- 201000010099 disease Diseases 0.000 description 26
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 26
- 241000209219 Hordeum Species 0.000 description 20
- 240000008067 Cucumis sativus Species 0.000 description 17
- 235000010799 Cucumis sativus var sativus Nutrition 0.000 description 15
- 240000007594 Oryza sativa Species 0.000 description 14
- 235000007164 Oryza sativa Nutrition 0.000 description 14
- 235000009566 rice Nutrition 0.000 description 13
- 240000003768 Solanum lycopersicum Species 0.000 description 11
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 10
- 206010039509 Scab Diseases 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- JEOVEEPACZXTPL-UHFFFAOYSA-N 1h-pyrazol-1-ium;perchlorate Chemical compound C1=CN[NH+]=C1.[O-]Cl(=O)(=O)=O JEOVEEPACZXTPL-UHFFFAOYSA-N 0.000 description 9
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 9
- ICIHDUSPYJNBRL-UHFFFAOYSA-N methyl sulfate;1h-pyrazol-1-ium Chemical compound [NH2+]1C=CC=N1.COS([O-])(=O)=O ICIHDUSPYJNBRL-UHFFFAOYSA-N 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 8
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 description 8
- 235000013532 brandy Nutrition 0.000 description 8
- 125000004172 4-methoxyphenyl group Chemical group [H]C1=C([H])C(OC([H])([H])[H])=C([H])C([H])=C1* 0.000 description 7
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 6
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- 241000233866 Fungi Species 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- JIJBWYXJIKAYLT-UHFFFAOYSA-N 1h-pyrazol-1-ium;iodide Chemical compound [I-].C1=CN[NH+]=C1 JIJBWYXJIKAYLT-UHFFFAOYSA-N 0.000 description 5
- 244000052769 pathogen Species 0.000 description 5
- 238000010992 reflux Methods 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- 238000005507 spraying Methods 0.000 description 5
- 239000004094 surface-active agent Substances 0.000 description 5
- LLIOTGIXSUTUJW-UHFFFAOYSA-K 1,2-dimethyl-3,5-diphenylpyrazol-1-ium phosphate Chemical compound P(=O)([O-])([O-])[O-].C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC=CC=C1)C.C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC=CC=C1)C.C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC=CC=C1)C LLIOTGIXSUTUJW-UHFFFAOYSA-K 0.000 description 4
- 231100000674 Phytotoxicity Toxicity 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 4
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 4
- 238000011156 evaluation Methods 0.000 description 4
- VHHIZTNRHSRKLY-UHFFFAOYSA-N methyl sulfate 1-phenyl-1H-pyrazol-1-ium Chemical compound S(=O)(=O)(OC)[O-].C1(=CC=CC=C1)[NH+]1N=CC=C1 VHHIZTNRHSRKLY-UHFFFAOYSA-N 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- MTCQFVYEKGHUGI-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;4-methylbenzenesulfonate Chemical compound CC1=CC=C(S([O-])(=O)=O)C=C1.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 MTCQFVYEKGHUGI-UHFFFAOYSA-M 0.000 description 3
- TWUBOZYAXNVYGS-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;iodide Chemical compound [I-].C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 TWUBOZYAXNVYGS-UHFFFAOYSA-M 0.000 description 3
- SVDTUJAQNAQGGW-UHFFFAOYSA-N 1-methyl-3,5-diphenylpyrazole Chemical compound CN1N=C(C=2C=CC=CC=2)C=C1C1=CC=CC=C1 SVDTUJAQNAQGGW-UHFFFAOYSA-N 0.000 description 3
- IRFOHPBZHGDLIP-UHFFFAOYSA-M 3-(4-fluorophenyl)-1,2-dimethyl-5-phenylpyrazol-1-ium methyl sulfate Chemical compound S(=O)(=O)(OC)[O-].FC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=CC=C1)C)C IRFOHPBZHGDLIP-UHFFFAOYSA-M 0.000 description 3
- 125000006305 3-iodophenyl group Chemical group [H]C1=C([H])C(I)=C([H])C(*)=C1[H] 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- BOYCWGXXIHBYJC-UHFFFAOYSA-M S(=O)(=O)(OC)[O-].C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC(=CC(=C1)C)C)C Chemical compound S(=O)(=O)(OC)[O-].C[N+]=1N(C(=CC1C1=CC=CC=C1)C1=CC(=CC(=C1)C)C)C BOYCWGXXIHBYJC-UHFFFAOYSA-M 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 230000029936 alkylation Effects 0.000 description 3
- 238000005804 alkylation reaction Methods 0.000 description 3
- 235000021016 apples Nutrition 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 238000009472 formulation Methods 0.000 description 3
- 238000002844 melting Methods 0.000 description 3
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- 239000011541 reaction mixture Substances 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- AQRAUYUNVFXIPS-UHFFFAOYSA-L 1,2-dimethyl-3,5-bis(2-methylphenyl)pyrazol-1-ium sulfate Chemical compound S(=O)(=O)([O-])[O-].C[N+]=1N(C(=CC1C1=C(C=CC=C1)C)C1=C(C=CC=C1)C)C.C[N+]=1N(C(=CC1C1=C(C=CC=C1)C)C1=C(C=CC=C1)C)C AQRAUYUNVFXIPS-UHFFFAOYSA-L 0.000 description 2
- QPHPWHYLXYFPHZ-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;bromide Chemical compound [Br-].C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 QPHPWHYLXYFPHZ-UHFFFAOYSA-M 0.000 description 2
- BGCSXGXXLDPSHB-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;hydroxide Chemical compound [OH-].C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 BGCSXGXXLDPSHB-UHFFFAOYSA-M 0.000 description 2
- XQEMNBNCQVQXMO-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;methyl sulfate Chemical compound COS([O-])(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 XQEMNBNCQVQXMO-UHFFFAOYSA-M 0.000 description 2
- VTWNZNWFJUMAOD-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium;perchlorate Chemical compound [O-]Cl(=O)(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 VTWNZNWFJUMAOD-UHFFFAOYSA-M 0.000 description 2
- CJCAUQXJUFZVFT-UHFFFAOYSA-N 1-phenyl-1H-pyrazol-1-ium perchlorate Chemical compound Cl(=O)(=O)(=O)[O-].C1(=CC=CC=C1)[NH+]1N=CC=C1 CJCAUQXJUFZVFT-UHFFFAOYSA-N 0.000 description 2
- RMOODAZDRQFBHD-UHFFFAOYSA-N 1-phenyl-1h-pyrazol-1-ium;iodide Chemical compound [I-].N1=CC=C[NH+]1C1=CC=CC=C1 RMOODAZDRQFBHD-UHFFFAOYSA-N 0.000 description 2
- AYYIPZWOCQOIBV-UHFFFAOYSA-L 3,5-bis(4-chlorophenyl)-1,2-dimethylpyrazol-1-ium sulfate Chemical compound S(=O)(=O)([O-])[O-].ClC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=C(C=C1)Cl)C)C.ClC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=C(C=C1)Cl)C)C AYYIPZWOCQOIBV-UHFFFAOYSA-L 0.000 description 2
- JXHKUYQCEJILEI-UHFFFAOYSA-N 3,5-diphenyl-1h-pyrazole Chemical compound C=1C(C=2C=CC=CC=2)=NNC=1C1=CC=CC=C1 JXHKUYQCEJILEI-UHFFFAOYSA-N 0.000 description 2
- AFFMRQYXUKNUMF-UHFFFAOYSA-M 3-(4-fluorophenyl)-1,2-dimethyl-5-phenylpyrazol-1-ium perchlorate Chemical compound Cl(=O)(=O)(=O)[O-].FC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=CC=C1)C)C AFFMRQYXUKNUMF-UHFFFAOYSA-M 0.000 description 2
- KPHQFTCCSHEJJC-UHFFFAOYSA-L 3-(4-fluorophenyl)-1,2-dimethyl-5-phenylpyrazol-1-ium sulfate Chemical compound S(=O)(=O)([O-])[O-].FC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=CC=C1)C)C.FC1=CC=C(C=C1)C=1N([N+](=C(C1)C1=CC=CC=C1)C)C KPHQFTCCSHEJJC-UHFFFAOYSA-L 0.000 description 2
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- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 2
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- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 description 2
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- 238000009833 condensation Methods 0.000 description 2
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- 125000005594 diketone group Chemical group 0.000 description 2
- 239000003085 diluting agent Substances 0.000 description 2
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- 238000011835 investigation Methods 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
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- 235000021017 pears Nutrition 0.000 description 2
- 239000002798 polar solvent Substances 0.000 description 2
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- VJTZIJOEPIURRT-UHFFFAOYSA-N (2-methylquinolin-8-yl) n-methylcarbamate Chemical compound C1=C(C)N=C2C(OC(=O)NC)=CC=CC2=C1 VJTZIJOEPIURRT-UHFFFAOYSA-N 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Chemical compound FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
- HFIVMLPKDPFIAU-UHFFFAOYSA-N 1,2-dimethyl-3,5-bis(4-methylphenyl)pyrazol-1-ium Chemical compound C[N+]=1N(C(=CC1C1=CC=C(C=C1)C)C1=CC=C(C=C1)C)C HFIVMLPKDPFIAU-UHFFFAOYSA-N 0.000 description 1
- MGSJXXVDLDJDBE-UHFFFAOYSA-M 1,2-dimethyl-3,5-bis(4-methylphenyl)pyrazol-1-ium 4-methylbenzenesulfonate Chemical compound C1(=CC=C(C=C1)S(=O)(=O)[O-])C.C[N+]=1N(C(=CC1C1=CC=C(C=C1)C)C1=CC=C(C=C1)C)C MGSJXXVDLDJDBE-UHFFFAOYSA-M 0.000 description 1
- HUWDEIJHVQPXBJ-UHFFFAOYSA-M 1,2-dimethyl-3,5-diphenylpyrazol-1-ium methanesulfonate Chemical compound CS([O-])(=O)=O.C[N+]=1N(C)C(C=2C=CC=CC=2)=CC=1C1=CC=CC=C1 HUWDEIJHVQPXBJ-UHFFFAOYSA-M 0.000 description 1
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Classifications
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- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US546654A US3930011A (en) | 1975-02-03 | 1975-02-03 | Pyrazolium fungicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE2602964A1 true DE2602964A1 (de) | 1976-08-05 |
Family
ID=24181410
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE19762602964 Withdrawn DE2602964A1 (de) | 1975-02-03 | 1976-01-27 | Fungicides mittel |
Country Status (25)
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4207326A (en) * | 1979-05-21 | 1980-06-10 | Cilag-Chemie A.G. | Antimicrobial quaternary pyrazole derivatives |
| US5470869A (en) * | 1994-01-31 | 1995-11-28 | American Cyanamid Company | Pyrazolium fungicidal compositions |
| GB2294640A (en) * | 1994-11-07 | 1996-05-08 | American Cyanamid Co | Synergistic fungicidal difenzoquat compositions |
| EP4173485A1 (en) * | 2021-10-27 | 2023-05-03 | Max-Planck-Gesellschaft zur Förderung der Wissenschaften e.V. | Protein aggregation inhibiting compounds for plant disease control |
-
1975
- 1975-02-03 US US546654A patent/US3930011A/en not_active Expired - Lifetime
- 1975-12-22 ZA ZA00757951A patent/ZA757951B/xx unknown
- 1975-12-23 IL IL48708A patent/IL48708A/xx unknown
- 1975-12-24 AU AU87903/75A patent/AU500653B2/en not_active Expired
- 1975-12-30 GB GB53214/75A patent/GB1534866A/en not_active Expired
-
1976
- 1976-01-09 CA CA243,287A patent/CA1058517A/en not_active Expired
- 1976-01-13 AR AR261918A patent/AR217624A1/es active
- 1976-01-19 IT IT47683/76A patent/IT1053334B/it active
- 1976-01-23 NL NL7600700A patent/NL7600700A/xx not_active Application Discontinuation
- 1976-01-26 DK DK29676AA patent/DK139833B/da not_active IP Right Cessation
- 1976-01-26 FI FI760174A patent/FI59194C/fi not_active IP Right Cessation
- 1976-01-27 TR TR18706A patent/TR18706A/xx unknown
- 1976-01-27 DE DE19762602964 patent/DE2602964A1/de not_active Withdrawn
- 1976-01-29 CS CS76580A patent/CS199651B2/cs unknown
- 1976-02-02 BR BR7600646A patent/BR7600646A/pt unknown
- 1976-02-02 NO NO760343A patent/NO145039C/no unknown
- 1976-02-02 AT AT69776A patent/AT347178B/de not_active IP Right Cessation
- 1976-02-02 SU SU762319208A patent/SU644359A3/ru active
- 1976-02-02 CH CH124376A patent/CH594354A5/xx not_active IP Right Cessation
- 1976-02-02 BE BE164007A patent/BE838171R/xx not_active IP Right Cessation
- 1976-02-02 SE SE7601095A patent/SE420888B/xx unknown
- 1976-02-03 JP JP51010777A patent/JPS51104031A/ja active Pending
- 1976-02-03 DD DD191070A patent/DD124703A6/xx unknown
- 1976-02-03 IE IE218/76A patent/IE42949B1/en unknown
- 1976-02-03 FR FR7602975A patent/FR2298949A2/fr active Granted
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| 8128 | New person/name/address of the agent |
Representative=s name: SPOTT, G., DIPL.-CHEM. DR.RER.NAT., PAT.-ANW., 800 |
|
| 8141 | Disposal/no request for examination |