HU187307B - Fungicide compositions containing derivatives of 2-sulphinyl-5-sulphonyl-1,3,4-thiadiazole derivatives - Google Patents
Fungicide compositions containing derivatives of 2-sulphinyl-5-sulphonyl-1,3,4-thiadiazole derivatives Download PDFInfo
- Publication number
- HU187307B HU187307B HU802006A HU200680A HU187307B HU 187307 B HU187307 B HU 187307B HU 802006 A HU802006 A HU 802006A HU 200680 A HU200680 A HU 200680A HU 187307 B HU187307 B HU 187307B
- Authority
- HU
- Hungary
- Prior art keywords
- thiadiazole
- active ingredient
- composition
- composition according
- methylsulfonyl
- Prior art date
Links
- BMRPEMSWZYKQQT-UHFFFAOYSA-N 2-sulfinyl-5-sulfonyl-1,3,4-thiadiazole Chemical class O=S=C1SC(=S(=O)=O)N=N1 BMRPEMSWZYKQQT-UHFFFAOYSA-N 0.000 title claims abstract 3
- 239000000203 mixture Substances 0.000 title claims 58
- 230000000855 fungicidal effect Effects 0.000 title claims 2
- 239000000417 fungicide Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 claims abstract 4
- 239000004480 active ingredient Substances 0.000 claims 56
- -1 η-butyl Chemical group 0.000 claims 6
- IAYDODCOMFBPJJ-UHFFFAOYSA-N 2-hexan-3-ylsulfinyl-5-propylsulfonyl-1,3,4-thiadiazole Chemical group CCCC(CC)S(=O)C1=NN=C(S(=O)(=O)CCC)S1 IAYDODCOMFBPJJ-UHFFFAOYSA-N 0.000 claims 2
- 239000007800 oxidant agent Substances 0.000 claims 2
- OXZNKVGGBZSMLO-UHFFFAOYSA-N 2-(2-methylpropylsulfinyl)-5-propan-2-ylsulfonyl-1,3,4-thiadiazole Chemical group CC(C)CS(=O)C1=NN=C(S(=O)(=O)C(C)C)S1 OXZNKVGGBZSMLO-UHFFFAOYSA-N 0.000 claims 1
- PEDQQTXSNKBWQP-UHFFFAOYSA-N 2-(2-methylpropylsulfonyl)-5-pentan-2-ylsulfinyl-1,3,4-thiadiazole Chemical group CCCC(C)S(=O)C1=NN=C(S(=O)(=O)CC(C)C)S1 PEDQQTXSNKBWQP-UHFFFAOYSA-N 0.000 claims 1
- FRVMWEULJJPYGK-UHFFFAOYSA-N 2-(3-methylbutylsulfinyl)-5-methylsulfonyl-1,3,4-thiadiazole Chemical group CC(C)CCS(=O)C1=NN=C(S(C)(=O)=O)S1 FRVMWEULJJPYGK-UHFFFAOYSA-N 0.000 claims 1
- NUWZCOSVISRBFO-UHFFFAOYSA-N 2-butan-2-ylsulfinyl-5-ethylsulfonyl-1,3,4-thiadiazole Chemical group CCC(C)S(=O)C1=NN=C(S(=O)(=O)CC)S1 NUWZCOSVISRBFO-UHFFFAOYSA-N 0.000 claims 1
- OKFWZZHWISHUOB-UHFFFAOYSA-N 2-butan-2-ylsulfinyl-5-methylsulfonyl-1,3,4-thiadiazole Chemical group CCC(C)S(=O)C1=NN=C(S(C)(=O)=O)S1 OKFWZZHWISHUOB-UHFFFAOYSA-N 0.000 claims 1
- AVVQPHWLVWTOQW-UHFFFAOYSA-N 2-butan-2-ylsulfonyl-5-ethylsulfinyl-1,3,4-thiadiazole Chemical group CCC(C)S(=O)(=O)C1=NN=C(S(=O)CC)S1 AVVQPHWLVWTOQW-UHFFFAOYSA-N 0.000 claims 1
- NZGWFZHNZSGBDV-UHFFFAOYSA-N 2-butan-2-ylsulfonyl-5-propan-2-ylsulfinyl-1,3,4-thiadiazole Chemical group CCC(C)S(=O)(=O)C1=NN=C(S(=O)C(C)C)S1 NZGWFZHNZSGBDV-UHFFFAOYSA-N 0.000 claims 1
- FIRCJMOVHDNGPX-UHFFFAOYSA-N 2-butylsulfinyl-5-butylsulfonyl-1,3,4-thiadiazole Chemical group CCCCS(=O)C1=NN=C(S(=O)(=O)CCCC)S1 FIRCJMOVHDNGPX-UHFFFAOYSA-N 0.000 claims 1
- IQELCNPNPCBLMV-UHFFFAOYSA-N 2-butylsulfinyl-5-ethylsulfonyl-1,3,4-thiadiazole Chemical group CCCCS(=O)C1=NN=C(S(=O)(=O)CC)S1 IQELCNPNPCBLMV-UHFFFAOYSA-N 0.000 claims 1
- MAFIAYOFZOVHTE-UHFFFAOYSA-N 2-butylsulfinyl-5-propan-2-ylsulfonyl-1,3,4-thiadiazole Chemical group CCCCS(=O)C1=NN=C(S(=O)(=O)C(C)C)S1 MAFIAYOFZOVHTE-UHFFFAOYSA-N 0.000 claims 1
- NOSUICBEXFNJGH-UHFFFAOYSA-N 2-butylsulfonyl-5-(2-methylpropylsulfinyl)-1,3,4-thiadiazole Chemical group CCCCS(=O)(=O)C1=NN=C(S(=O)CC(C)C)S1 NOSUICBEXFNJGH-UHFFFAOYSA-N 0.000 claims 1
- KHTPKAHRHJHTPM-UHFFFAOYSA-N 2-butylsulfonyl-5-ethylsulfinyl-1,3,4-thiadiazole Chemical group CCCCS(=O)(=O)C1=NN=C(S(=O)CC)S1 KHTPKAHRHJHTPM-UHFFFAOYSA-N 0.000 claims 1
- ZUEUFSXKWOYTKA-UHFFFAOYSA-N 2-butylsulfonyl-5-hexan-3-ylsulfinyl-1,3,4-thiadiazole Chemical group CCCCS(=O)(=O)C1=NN=C(S(=O)C(CC)CCC)S1 ZUEUFSXKWOYTKA-UHFFFAOYSA-N 0.000 claims 1
- JPGSOGXYMCLOPY-UHFFFAOYSA-N 2-butylsulfonyl-5-methylsulfinyl-1,3,4-thiadiazole Chemical group CCCCS(=O)(=O)C1=NN=C(S(C)=O)S1 JPGSOGXYMCLOPY-UHFFFAOYSA-N 0.000 claims 1
- PPWUERZSPLGAAW-UHFFFAOYSA-N 2-butylsulfonyl-5-methylsulfonyl-1,3,4-thiadiazole Chemical group C(CCC)S(=O)(=O)C=1SC(=NN1)S(=O)(=O)C PPWUERZSPLGAAW-UHFFFAOYSA-N 0.000 claims 1
- RPQOWKFNPCDCQU-UHFFFAOYSA-N 2-butylsulfonyl-5-pentan-2-ylsulfinyl-1,3,4-thiadiazole Chemical group CCCCS(=O)(=O)C1=NN=C(S(=O)C(C)CCC)S1 RPQOWKFNPCDCQU-UHFFFAOYSA-N 0.000 claims 1
- KFWIMKABUKCBTE-UHFFFAOYSA-N 2-butylsulfonyl-5-pentylsulfinyl-1,3,4-thiadiazole Chemical compound CCCCCS(=O)C1=NN=C(S(=O)(=O)CCCC)S1 KFWIMKABUKCBTE-UHFFFAOYSA-N 0.000 claims 1
- SNYINMLGIJCRPM-UHFFFAOYSA-N 2-butylsulfonyl-5-propan-2-ylsulfinyl-1,3,4-thiadiazole Chemical group CCCCS(=O)(=O)C1=NN=C(S(=O)C(C)C)S1 SNYINMLGIJCRPM-UHFFFAOYSA-N 0.000 claims 1
- DPUWPAJEQCRLSZ-UHFFFAOYSA-N 2-butylsulfonyl-5-propylsulfinyl-1,3,4-thiadiazole Chemical group CCCCS(=O)(=O)C1=NN=C(S(=O)CCC)S1 DPUWPAJEQCRLSZ-UHFFFAOYSA-N 0.000 claims 1
- XBFCRPIQQIGUIG-UHFFFAOYSA-N 2-ethylsulfinyl-5-ethylsulfonyl-1,3,4-thiadiazole Chemical group CCS(=O)C1=NN=C(S(=O)(=O)CC)S1 XBFCRPIQQIGUIG-UHFFFAOYSA-N 0.000 claims 1
- WETWGXOLHHYKCX-UHFFFAOYSA-N 2-ethylsulfinyl-5-methylsulfonyl-1,3,4-thiadiazole Chemical group CCS(=O)C1=NN=C(S(C)(=O)=O)S1 WETWGXOLHHYKCX-UHFFFAOYSA-N 0.000 claims 1
- CQDUYBOPLXMQMC-UHFFFAOYSA-N 2-ethylsulfinyl-5-propan-2-ylsulfonyl-1,3,4-thiadiazole Chemical group CCS(=O)C1=NN=C(S(=O)(=O)C(C)C)S1 CQDUYBOPLXMQMC-UHFFFAOYSA-N 0.000 claims 1
- RBIAQLWNDOFYTG-UHFFFAOYSA-N 2-ethylsulfinyl-5-propylsulfonyl-1,3,4-thiadiazole Chemical group CCCS(=O)(=O)C1=NN=C(S(=O)CC)S1 RBIAQLWNDOFYTG-UHFFFAOYSA-N 0.000 claims 1
- DMKBVKQFXJVBRZ-UHFFFAOYSA-N 2-ethylsulfonyl-5-(2-methylpropylsulfinyl)-1,3,4-thiadiazole Chemical group CCS(=O)(=O)C1=NN=C(S(=O)CC(C)C)S1 DMKBVKQFXJVBRZ-UHFFFAOYSA-N 0.000 claims 1
- QMJCWAVJMZWBJA-UHFFFAOYSA-N 2-ethylsulfonyl-5-hexan-3-ylsulfinyl-1,3,4-thiadiazole Chemical group CCCC(CC)S(=O)C1=NN=C(S(=O)(=O)CC)S1 QMJCWAVJMZWBJA-UHFFFAOYSA-N 0.000 claims 1
- HDUTXMKPXUEOLB-UHFFFAOYSA-N 2-ethylsulfonyl-5-hexylsulfinyl-1,3,4-thiadiazole Chemical group CCCCCCS(=O)C1=NN=C(S(=O)(=O)CC)S1 HDUTXMKPXUEOLB-UHFFFAOYSA-N 0.000 claims 1
- CSQIUYCTHDBODM-UHFFFAOYSA-N 2-ethylsulfonyl-5-pentan-2-ylsulfinyl-1,3,4-thiadiazole Chemical group CCCC(C)S(=O)C1=NN=C(S(=O)(=O)CC)S1 CSQIUYCTHDBODM-UHFFFAOYSA-N 0.000 claims 1
- YUUGSMJRZQZHQP-UHFFFAOYSA-N 2-ethylsulfonyl-5-pentylsulfinyl-1,3,4-thiadiazole Chemical group CCCCCS(=O)C1=NN=C(S(=O)(=O)CC)S1 YUUGSMJRZQZHQP-UHFFFAOYSA-N 0.000 claims 1
- LLZCEECLPNHQIG-UHFFFAOYSA-N 2-ethylsulfonyl-5-propan-2-ylsulfinyl-1,3,4-thiadiazole Chemical group CCS(=O)(=O)C1=NN=C(S(=O)C(C)C)S1 LLZCEECLPNHQIG-UHFFFAOYSA-N 0.000 claims 1
- VWKRWYHWRYJFQO-UHFFFAOYSA-N 2-ethylsulfonyl-5-propylsulfinyl-1,3,4-thiadiazole Chemical group CCCS(=O)C1=NN=C(S(=O)(=O)CC)S1 VWKRWYHWRYJFQO-UHFFFAOYSA-N 0.000 claims 1
- VCHGICVYQBQSBI-UHFFFAOYSA-N 2-hexan-3-ylsulfinyl-5-(2-methylpropylsulfonyl)-1,3,4-thiadiazole Chemical group CCCC(CC)S(=O)C1=NN=C(S(=O)(=O)CC(C)C)S1 VCHGICVYQBQSBI-UHFFFAOYSA-N 0.000 claims 1
- POEJXWFVBJVAIE-UHFFFAOYSA-N 2-hexan-3-ylsulfinyl-5-methylsulfonyl-1,3,4-thiadiazole Chemical group CCCC(CC)S(=O)C1=NN=C(S(C)(=O)=O)S1 POEJXWFVBJVAIE-UHFFFAOYSA-N 0.000 claims 1
- VPPKETKQKPPHHY-UHFFFAOYSA-N 2-hexan-3-ylsulfinyl-5-pentylsulfonyl-1,3,4-thiadiazole Chemical group CCCCCS(=O)(=O)C1=NN=C(S(=O)C(CC)CCC)S1 VPPKETKQKPPHHY-UHFFFAOYSA-N 0.000 claims 1
- QTQLTIZUYBYYRE-UHFFFAOYSA-N 2-hexylsulfinyl-5-methylsulfonyl-1,3,4-thiadiazole Chemical group CCCCCCS(=O)C1=NN=C(S(C)(=O)=O)S1 QTQLTIZUYBYYRE-UHFFFAOYSA-N 0.000 claims 1
- BHCLDIZCCKZBHT-UHFFFAOYSA-N 2-methylsulfinyl-5-methylsulfonyl-1,3,4-thiadiazole Chemical group CS(=O)C1=NN=C(S(C)(=O)=O)S1 BHCLDIZCCKZBHT-UHFFFAOYSA-N 0.000 claims 1
- WMXKNGCDYWFKLG-UHFFFAOYSA-N 2-methylsulfinyl-5-propan-2-ylsulfonyl-1,3,4-thiadiazole Chemical group CC(C)S(=O)(=O)C1=NN=C(S(C)=O)S1 WMXKNGCDYWFKLG-UHFFFAOYSA-N 0.000 claims 1
- FFXYPUDZVDLVCF-UHFFFAOYSA-N 2-methylsulfinyl-5-propylsulfonyl-1,3,4-thiadiazole Chemical group CCCS(=O)(=O)C1=NN=C(S(C)=O)S1 FFXYPUDZVDLVCF-UHFFFAOYSA-N 0.000 claims 1
- FGGYLEBTLKZNNP-UHFFFAOYSA-N 2-methylsulfonyl-5-pentan-2-ylsulfinyl-1,3,4-thiadiazole Chemical group CCCC(C)S(=O)C1=NN=C(S(C)(=O)=O)S1 FGGYLEBTLKZNNP-UHFFFAOYSA-N 0.000 claims 1
- FBXSDUZXZCIJSQ-UHFFFAOYSA-N 2-methylsulfonyl-5-pentylsulfinyl-1,3,4-thiadiazole Chemical group CCCCCS(=O)C1=NN=C(S(C)(=O)=O)S1 FBXSDUZXZCIJSQ-UHFFFAOYSA-N 0.000 claims 1
- QVVGWRMQWDVYFB-UHFFFAOYSA-N 2-methylsulfonyl-5-propan-2-ylsulfinyl-1,3,4-thiadiazole Chemical group CC(C)S(=O)C1=NN=C(S(C)(=O)=O)S1 QVVGWRMQWDVYFB-UHFFFAOYSA-N 0.000 claims 1
- HQRHFLDRZBPWBZ-UHFFFAOYSA-N 2-methylsulfonyl-5-propylsulfinyl-1,3,4-thiadiazole Chemical group CCCS(=O)C1=NN=C(S(C)(=O)=O)S1 HQRHFLDRZBPWBZ-UHFFFAOYSA-N 0.000 claims 1
- RJDUNFDPHWIGFY-UHFFFAOYSA-N 2-pentan-2-ylsulfinyl-5-pentylsulfonyl-1,3,4-thiadiazole Chemical group CCCCCS(=O)(=O)C1=NN=C(S(=O)C(C)CCC)S1 RJDUNFDPHWIGFY-UHFFFAOYSA-N 0.000 claims 1
- ZAIHOYZLUDPCEC-UHFFFAOYSA-N 2-pentan-2-ylsulfinyl-5-propylsulfonyl-1,3,4-thiadiazole Chemical group CCCC(C)S(=O)C1=NN=C(S(=O)(=O)CCC)S1 ZAIHOYZLUDPCEC-UHFFFAOYSA-N 0.000 claims 1
- FLKKIUARSRWBEN-UHFFFAOYSA-N 2-propan-2-ylsulfinyl-5-propan-2-ylsulfonyl-1,3,4-thiadiazole Chemical group CC(C)S(=O)C1=NN=C(S(=O)(=O)C(C)C)S1 FLKKIUARSRWBEN-UHFFFAOYSA-N 0.000 claims 1
- IYOYGOWRCPRNDX-UHFFFAOYSA-N 2-propan-2-ylsulfonyl-5-propylsulfinyl-1,3,4-thiadiazole Chemical group CCCS(=O)C1=NN=C(S(=O)(=O)C(C)C)S1 IYOYGOWRCPRNDX-UHFFFAOYSA-N 0.000 claims 1
- PSQSCMSKPVABTH-UHFFFAOYSA-N 2-tert-butylsulfinyl-5-butylsulfonyl-1,3,4-thiadiazole Chemical compound CCCCS(=O)(=O)C1=NN=C(S(=O)C(C)(C)C)S1 PSQSCMSKPVABTH-UHFFFAOYSA-N 0.000 claims 1
- ARQKYJJYSQTKBO-UHFFFAOYSA-N 2-tert-butylsulfinyl-5-ethylsulfonyl-1,3,4-thiadiazole Chemical group CCS(=O)(=O)C1=NN=C(S(=O)C(C)(C)C)S1 ARQKYJJYSQTKBO-UHFFFAOYSA-N 0.000 claims 1
- FGRSUHPDMSODKG-UHFFFAOYSA-N 2-tert-butylsulfinyl-5-methylsulfonyl-1,3,4-thiadiazole Chemical group CC(C)(C)S(=O)C1=NN=C(S(C)(=O)=O)S1 FGRSUHPDMSODKG-UHFFFAOYSA-N 0.000 claims 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 229910052783 alkali metal Inorganic materials 0.000 claims 1
- 229910052791 calcium Inorganic materials 0.000 claims 1
- 239000011575 calcium Substances 0.000 claims 1
- 235000014113 dietary fatty acids Nutrition 0.000 claims 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000006125 ethylsulfonyl group Chemical group 0.000 claims 1
- 239000000194 fatty acid Substances 0.000 claims 1
- 229930195729 fatty acid Natural products 0.000 claims 1
- 150000004665 fatty acids Chemical class 0.000 claims 1
- 150000002191 fatty alcohols Chemical class 0.000 claims 1
- 150000002432 hydroperoxides Chemical class 0.000 claims 1
- 239000012442 inert solvent Substances 0.000 claims 1
- 229910052500 inorganic mineral Inorganic materials 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 claims 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 229920005610 lignin Polymers 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 239000011707 mineral Substances 0.000 claims 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 claims 1
- 150000007530 organic bases Chemical class 0.000 claims 1
- 239000003960 organic solvent Substances 0.000 claims 1
- 150000004965 peroxy acids Chemical class 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 239000007787 solid Substances 0.000 claims 1
- 239000004094 surface-active agent Substances 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 101100072620 Streptomyces griseus ind2 gene Proteins 0.000 abstract 2
- 241000233866 Fungi Species 0.000 abstract 1
- 125000003342 alkenyl group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 0.000 abstract 1
- 235000013339 cereals Nutrition 0.000 abstract 1
- 239000003795 chemical substances by application Substances 0.000 abstract 1
- 230000000973 chemotherapeutic effect Effects 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 230000007613 environmental effect Effects 0.000 abstract 1
- 238000003898 horticulture Methods 0.000 abstract 1
- 239000000126 substance Substances 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D285/00—Heterocyclic compounds containing rings having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by groups C07D275/00 - C07D283/00
- C07D285/01—Five-membered rings
- C07D285/02—Thiadiazoles; Hydrogenated thiadiazoles
- C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
- C07D285/12—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles
- C07D285/125—1,3,4-Thiadiazoles; Hydrogenated 1,3,4-thiadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
-
- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792933008 DE2933008A1 (de) | 1979-08-13 | 1979-08-13 | 2-sulfinyl-5-sulfonyl-1,3,4-thiadiazolderivate, verfahren zur herstellung dieser verbindungen sowie diese enthaltende fungizide mittel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| HU187307B true HU187307B (en) | 1985-12-28 |
Family
ID=6078481
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| HU802006A HU187307B (en) | 1979-08-13 | 1980-08-12 | Fungicide compositions containing derivatives of 2-sulphinyl-5-sulphonyl-1,3,4-thiadiazole derivatives |
Country Status (39)
| Country | Link |
|---|---|
| US (1) | US4369185A (OSRAM) |
| JP (1) | JPS5629580A (OSRAM) |
| AR (1) | AR224906A1 (OSRAM) |
| AT (1) | AT366888B (OSRAM) |
| AU (1) | AU533363B2 (OSRAM) |
| BE (1) | BE884764A (OSRAM) |
| BR (1) | BR8005061A (OSRAM) |
| CA (1) | CA1146946A (OSRAM) |
| CH (1) | CH645366A5 (OSRAM) |
| CS (1) | CS212722B2 (OSRAM) |
| DD (1) | DD152468A5 (OSRAM) |
| DE (1) | DE2933008A1 (OSRAM) |
| DK (1) | DK327780A (OSRAM) |
| EG (1) | EG14322A (OSRAM) |
| ES (1) | ES494075A0 (OSRAM) |
| FI (1) | FI802537A7 (OSRAM) |
| FR (1) | FR2463133A1 (OSRAM) |
| GB (1) | GB2058058B (OSRAM) |
| GR (1) | GR69848B (OSRAM) |
| HU (1) | HU187307B (OSRAM) |
| IE (1) | IE50105B1 (OSRAM) |
| IL (1) | IL60823A (OSRAM) |
| IT (1) | IT1132389B (OSRAM) |
| LU (1) | LU82703A1 (OSRAM) |
| MA (1) | MA18933A1 (OSRAM) |
| MX (1) | MX6142E (OSRAM) |
| NL (1) | NL8004440A (OSRAM) |
| NO (1) | NO150437C (OSRAM) |
| NZ (1) | NZ194566A (OSRAM) |
| PH (1) | PH17442A (OSRAM) |
| PL (1) | PL124268B1 (OSRAM) |
| PT (1) | PT71673B (OSRAM) |
| RO (1) | RO80302A (OSRAM) |
| SE (1) | SE440502B (OSRAM) |
| SU (1) | SU927115A3 (OSRAM) |
| TR (1) | TR20990A (OSRAM) |
| YU (1) | YU190380A (OSRAM) |
| ZA (1) | ZA804950B (OSRAM) |
| ZW (1) | ZW18880A1 (OSRAM) |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1695847C3 (de) * | 1967-06-09 | 1978-09-21 | Schering Ag, 1000 Berlin Und 4619 Bergkamen | 2,5-Alkyl-bzw.-ChloralkylsuUonyl-13,4-thiadiazole |
| NL6713712A (OSRAM) * | 1967-10-10 | 1969-04-14 | ||
| DE2533605A1 (de) * | 1975-07-26 | 1977-02-03 | Bayer Ag | Antiparasitenmittel |
-
1979
- 1979-08-13 DE DE19792933008 patent/DE2933008A1/de not_active Withdrawn
-
1980
- 1980-07-15 CH CH543580A patent/CH645366A5/de not_active IP Right Cessation
- 1980-07-25 SE SE8005391A patent/SE440502B/sv unknown
- 1980-07-28 YU YU01903/80A patent/YU190380A/xx unknown
- 1980-07-30 DK DK327780A patent/DK327780A/da unknown
- 1980-08-04 NL NL8004440A patent/NL8004440A/nl not_active Application Discontinuation
- 1980-08-05 NZ NZ194566A patent/NZ194566A/xx unknown
- 1980-08-07 RO RO80101925A patent/RO80302A/ro unknown
- 1980-08-07 MX MX808964U patent/MX6142E/es unknown
- 1980-08-08 PT PT71673A patent/PT71673B/pt unknown
- 1980-08-08 ES ES494075A patent/ES494075A0/es active Granted
- 1980-08-08 TR TR20990A patent/TR20990A/xx unknown
- 1980-08-09 MA MA19134A patent/MA18933A1/fr unknown
- 1980-08-09 EG EG481/80A patent/EG14322A/xx active
- 1980-08-11 PL PL1980226188A patent/PL124268B1/pl unknown
- 1980-08-11 DD DD80223242A patent/DD152468A5/de unknown
- 1980-08-11 IT IT24108/80A patent/IT1132389B/it active
- 1980-08-11 JP JP10934380A patent/JPS5629580A/ja active Pending
- 1980-08-11 GB GB8026125A patent/GB2058058B/en not_active Expired
- 1980-08-11 AR AR282117A patent/AR224906A1/es active
- 1980-08-11 GR GR62643A patent/GR69848B/el unknown
- 1980-08-11 LU LU82703A patent/LU82703A1/de unknown
- 1980-08-11 SU SU802959549A patent/SU927115A3/ru active
- 1980-08-12 IL IL60823A patent/IL60823A/xx unknown
- 1980-08-12 CA CA000358074A patent/CA1146946A/en not_active Expired
- 1980-08-12 US US06/178,703 patent/US4369185A/en not_active Expired - Lifetime
- 1980-08-12 AT AT0413480A patent/AT366888B/de not_active IP Right Cessation
- 1980-08-12 HU HU802006A patent/HU187307B/hu unknown
- 1980-08-12 AU AU61382/80A patent/AU533363B2/en not_active Ceased
- 1980-08-12 FI FI802537A patent/FI802537A7/fi not_active Application Discontinuation
- 1980-08-12 NO NO802405A patent/NO150437C/no unknown
- 1980-08-12 BR BR8005061A patent/BR8005061A/pt unknown
- 1980-08-13 BE BE0/201744A patent/BE884764A/fr not_active IP Right Cessation
- 1980-08-13 CS CS805585A patent/CS212722B2/cs unknown
- 1980-08-13 ZW ZW188/80A patent/ZW18880A1/xx unknown
- 1980-08-13 ZA ZA00804950A patent/ZA804950B/xx unknown
- 1980-08-13 IE IE1702/80A patent/IE50105B1/en unknown
- 1980-08-13 FR FR8017906A patent/FR2463133A1/fr active Granted
- 1980-08-13 PH PH24441A patent/PH17442A/en unknown
Also Published As
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| HU185231B (en) | Pesticide composition and process for preparing new pyridyl-aniline derivatives applicable as the active substances of the composition | |
| BR112018012717B1 (pt) | Composto de éter de malononitrila oxima e uso do mesmo | |
| JP2764265B2 (ja) | 殺微生物剤組成物 | |
| CS221944B2 (en) | Fungicide and/or bacteriocide means and method of making the active substances | |
| CS211368B2 (en) | Means with herbicide,growth regulating,fungicide effect | |
| GB2043062A (en) | N-(heterocyclyl)-acetanilide derivatives and herbicidal and plant growth regulating compositions containing them | |
| CS201517B2 (en) | Fungicide means | |
| CS205149B2 (en) | Herbicide,insecticide,fungicide or nematocide means and method of making the active substance | |
| HU190582B (en) | Agricultural and horticultural fungicide and nematocide compositions containing n,n-disubstituted azole-carbox-amide derivatives and process for producing these compounds | |
| DK149363B (da) | N-(1'-alkylthiocarbonyl-ethyl)-n-acetyl-anilinderivater til anvendelse til bekaempelse af fytopatogene svampe samt middel og fremgangsmaade til bekaempelse af fytopatogene svampe | |
| HU187307B (en) | Fungicide compositions containing derivatives of 2-sulphinyl-5-sulphonyl-1,3,4-thiadiazole derivatives | |
| JPH0248572A (ja) | 新規なチアゾール化合物及びその製造方法並びに該化合物を有効成分とする殺菌剤組成物 | |
| PL130882B1 (en) | Fungicidal,microbial and technical materials protectingagent and method of manufacture of novel n-sulfenylated benzylsulfonamides | |
| SU849976A3 (ru) | Фунгицидоинсектицидное средство | |
| US3660410A (en) | N-acyl-para-dialkylaminophenyl-hydrazones | |
| US3658992A (en) | Sulfamide derivatives | |
| JPH08507500A (ja) | 有害生物防除剤として有用なピリミジン誘導体 | |
| US3927220A (en) | Method of controlling pests with thioureido sulfonanilide compounds | |
| US4086360A (en) | Phenyl thiol carbanilide derivatives, method for the preparation thereof and use thereof as fungicide for agriculture | |
| KR840001934B1 (ko) | 2-설피닐-5-설포닐-1,3,4-티아디아졸 유도체의 제조방법 | |
| US4008318A (en) | Phosphorylated thiourea fungicides | |
| PL80657B1 (OSRAM) | ||
| HU182612B (en) | Fungicide compositions containing acetanilide derivatives as active agents, and process for producing these active agents | |
| US3927219A (en) | Method of controlling pests with thioureido carbamates compounds | |
| US3865809A (en) | O-(n-methylthiocarbamoyl)-hexamethylenimine-2-oxime |