FI70889C - Saosom insekticida medel anvaendbara tiazolyliden-oxo-propionitriler och foerfarande foer deras framstaellning - Google Patents
Saosom insekticida medel anvaendbara tiazolyliden-oxo-propionitriler och foerfarande foer deras framstaellning Download PDFInfo
- Publication number
- FI70889C FI70889C FI801379A FI801379A FI70889C FI 70889 C FI70889 C FI 70889C FI 801379 A FI801379 A FI 801379A FI 801379 A FI801379 A FI 801379A FI 70889 C FI70889 C FI 70889C
- Authority
- FI
- Finland
- Prior art keywords
- ylidene
- dihydrothiazol
- oxopropionitrile
- oxo
- methylphenyl
- Prior art date
Links
- 239000002917 insecticide Substances 0.000 title claims description 3
- -1 methoxyphenyl Chemical group 0.000 claims description 15
- 238000002360 preparation method Methods 0.000 claims description 10
- 239000002253 acid Substances 0.000 claims description 5
- 125000005059 halophenyl group Chemical group 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 5
- 125000003944 tolyl group Chemical group 0.000 claims description 5
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 4
- QLBGFCHJCWNVIN-UHFFFAOYSA-N 2-(1,3-thiazol-2-yl)acetonitrile Chemical compound N#CCC1=NC=CS1 QLBGFCHJCWNVIN-UHFFFAOYSA-N 0.000 claims description 3
- 239000001257 hydrogen Substances 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 239000012442 inert solvent Substances 0.000 claims description 3
- 150000007530 organic bases Chemical class 0.000 claims description 3
- 125000004076 pyridyl group Chemical group 0.000 claims description 3
- 125000001544 thienyl group Chemical group 0.000 claims description 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- 239000000460 chlorine Substances 0.000 claims description 2
- 229910052801 chlorine Inorganic materials 0.000 claims description 2
- 150000004820 halides Chemical class 0.000 claims description 2
- 229910052736 halogen Inorganic materials 0.000 claims description 2
- 150000002367 halogens Chemical group 0.000 claims description 2
- 150000002431 hydrogen Chemical class 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 description 24
- 125000004182 2-chlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(*)C([H])=C1[H] 0.000 description 11
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 8
- VHYFNPMBLIVWCW-UHFFFAOYSA-N 4-Dimethylaminopyridine Chemical compound CN(C)C1=CC=NC=C1 VHYFNPMBLIVWCW-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- ZMMOYIXZGHJMNI-UHFFFAOYSA-N 3-oxopropanenitrile Chemical compound O=CCC#N ZMMOYIXZGHJMNI-UHFFFAOYSA-N 0.000 description 4
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 4
- 239000000969 carrier Substances 0.000 description 4
- 230000000749 insecticidal effect Effects 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 239000000203 mixture Substances 0.000 description 4
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 description 4
- 239000013558 reference substance Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000007921 spray Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- GMFPOXMOLKOSIL-UHFFFAOYSA-N 3-(2-chlorophenyl)-2-[4-(2-methylphenyl)-3h-1,3-thiazol-2-ylidene]-3-oxopropanenitrile Chemical compound CC1=CC=CC=C1C(N1)=CSC1=C(C#N)C(=O)C1=CC=CC=C1Cl GMFPOXMOLKOSIL-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 239000007900 aqueous suspension Substances 0.000 description 3
- 239000003814 drug Substances 0.000 description 3
- 229940079593 drug Drugs 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000008018 melting Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 239000000725 suspension Substances 0.000 description 3
- 239000008096 xylene Substances 0.000 description 3
- UQISVQVOVFZPGU-UHFFFAOYSA-N 2-(4-tert-butyl-1,3-thiazol-2-yl)acetonitrile Chemical compound CC(C)(C)C1=CSC(CC#N)=N1 UQISVQVOVFZPGU-UHFFFAOYSA-N 0.000 description 2
- RSKYNAYOSJBNHL-UHFFFAOYSA-N 2-(4-tert-butyl-3h-1,3-thiazol-2-ylidene)-3-(2-chloro-6-fluorophenyl)-3-oxopropanenitrile Chemical compound N1C(C(C)(C)C)=CSC1=C(C#N)C(=O)C1=C(F)C=CC=C1Cl RSKYNAYOSJBNHL-UHFFFAOYSA-N 0.000 description 2
- DXARVPLVSAIPOK-UHFFFAOYSA-N 2-(4-tert-butyl-3h-1,3-thiazol-2-ylidene)-3-oxo-3-[2-(trifluoromethyl)phenyl]propanenitrile Chemical compound N1C(C(C)(C)C)=CSC1=C(C#N)C(=O)C1=CC=CC=C1C(F)(F)F DXARVPLVSAIPOK-UHFFFAOYSA-N 0.000 description 2
- 125000006276 2-bromophenyl group Chemical group [H]C1=C([H])C(Br)=C(*)C([H])=C1[H] 0.000 description 2
- BHPYMZQTCPRLNR-UHFFFAOYSA-N 2-cyanoethanethioamide Chemical compound NC(=S)CC#N BHPYMZQTCPRLNR-UHFFFAOYSA-N 0.000 description 2
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 description 2
- 125000006304 2-iodophenyl group Chemical group [H]C1=C([H])C(I)=C(*)C([H])=C1[H] 0.000 description 2
- 125000004204 2-methoxyphenyl group Chemical group [H]C1=C([H])C(*)=C(OC([H])([H])[H])C([H])=C1[H] 0.000 description 2
- OAQHSVDPXGIVIF-UHFFFAOYSA-N 3-(2-chloro-6-fluorophenyl)-2-[4-(2-methylphenyl)-3h-1,3-thiazol-2-ylidene]-3-oxopropanenitrile Chemical compound CC1=CC=CC=C1C(N1)=CSC1=C(C#N)C(=O)C1=C(F)C=CC=C1Cl OAQHSVDPXGIVIF-UHFFFAOYSA-N 0.000 description 2
- ACRWYXSKEHUQDB-UHFFFAOYSA-N 3-phenylpropionitrile Chemical compound N#CCCC1=CC=CC=C1 ACRWYXSKEHUQDB-UHFFFAOYSA-N 0.000 description 2
- 240000007124 Brassica oleracea Species 0.000 description 2
- 235000003899 Brassica oleracea var acephala Nutrition 0.000 description 2
- 235000011299 Brassica oleracea var botrytis Nutrition 0.000 description 2
- 235000011301 Brassica oleracea var capitata Nutrition 0.000 description 2
- 235000001169 Brassica oleracea var oleracea Nutrition 0.000 description 2
- 240000003259 Brassica oleracea var. botrytis Species 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241000238631 Hexapoda Species 0.000 description 2
- 241000500437 Plutella xylostella Species 0.000 description 2
- 239000004793 Polystyrene Substances 0.000 description 2
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 2
- WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- 150000001447 alkali salts Chemical class 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 2
- 235000019341 magnesium sulphate Nutrition 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 239000012074 organic phase Substances 0.000 description 2
- 229920002223 polystyrene Polymers 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 238000001228 spectrum Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- WBYWAXJHAXSJNI-VOTSOKGWSA-M .beta-Phenylacrylic acid Natural products [O-]C(=O)\C=C\C1=CC=CC=C1 WBYWAXJHAXSJNI-VOTSOKGWSA-M 0.000 description 1
- SAIRZMWXVJEBMO-UHFFFAOYSA-N 1-bromo-3,3-dimethylbutan-2-one Chemical compound CC(C)(C)C(=O)CBr SAIRZMWXVJEBMO-UHFFFAOYSA-N 0.000 description 1
- MJYIMIYVZNWWRE-UHFFFAOYSA-N 2,4,3$l^{4}-benzodioxathiepine 3-oxide Chemical compound O1S(=O)OC=C2C=CC=CC2=C1 MJYIMIYVZNWWRE-UHFFFAOYSA-N 0.000 description 1
- UYKNWJQVKVCCIQ-UHFFFAOYSA-N 2-(4-tert-butyl-3h-1,3-thiazol-2-ylidene)-3-(2-chlorophenyl)-3-oxopropanenitrile Chemical compound N1C(C(C)(C)C)=CSC1=C(C#N)C(=O)C1=CC=CC=C1Cl UYKNWJQVKVCCIQ-UHFFFAOYSA-N 0.000 description 1
- WOUKFFGCXATUQM-UHFFFAOYSA-N 2-(4-tert-butyl-3h-1,3-thiazol-2-ylidene)-3-(2-fluorophenyl)-3-oxopropanenitrile Chemical compound N1C(C(C)(C)C)=CSC1=C(C#N)C(=O)C1=CC=CC=C1F WOUKFFGCXATUQM-UHFFFAOYSA-N 0.000 description 1
- KSUYJGJINOBZNY-UHFFFAOYSA-N 2-(5-bromo-4-phenyl-3h-1,3-thiazol-2-ylidene)-3-(2-chlorophenyl)-3-oxopropanenitrile Chemical compound ClC1=CC=CC=C1C(=O)C(C#N)=C1SC(Br)=C(C=2C=CC=CC=2)N1 KSUYJGJINOBZNY-UHFFFAOYSA-N 0.000 description 1
- NUVDVYRBDIOXRJ-UHFFFAOYSA-N 2-[4-(2-methylphenyl)-1,3-thiazol-2-yl]acetonitrile Chemical compound CC1=CC=CC=C1C1=CSC(CC#N)=N1 NUVDVYRBDIOXRJ-UHFFFAOYSA-N 0.000 description 1
- GFNAJZAKJGKJCS-UHFFFAOYSA-N 2-chloro-6-fluorobenzoyl chloride Chemical compound FC1=CC=CC(Cl)=C1C(Cl)=O GFNAJZAKJGKJCS-UHFFFAOYSA-N 0.000 description 1
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- DNNHLQNVFDBOEC-UHFFFAOYSA-N 3-(2-bromophenyl)-3-oxo-2-(4-thiophen-2-yl-3h-1,3-thiazol-2-ylidene)propanenitrile Chemical compound BrC1=CC=CC=C1C(=O)C(C#N)=C1SC=C(C=2SC=CC=2)N1 DNNHLQNVFDBOEC-UHFFFAOYSA-N 0.000 description 1
- CRHSNTJEBKHSNH-UHFFFAOYSA-N 3-(2-chlorophenyl)-2-[4-(2-chlorophenyl)-3h-1,3-thiazol-2-ylidene]-3-oxopropanenitrile Chemical compound ClC1=CC=CC=C1C(=O)C(C#N)=C1SC=C(C=2C(=CC=CC=2)Cl)N1 CRHSNTJEBKHSNH-UHFFFAOYSA-N 0.000 description 1
- QYXYIHPHJILFDU-UHFFFAOYSA-N 3-(2-chlorophenyl)-2-[4-(2-fluorophenyl)-3h-1,3-thiazol-2-ylidene]-3-oxopropanenitrile Chemical compound FC1=CC=CC=C1C(N1)=CSC1=C(C#N)C(=O)C1=CC=CC=C1Cl QYXYIHPHJILFDU-UHFFFAOYSA-N 0.000 description 1
- QOZUJMONBWCZBM-UHFFFAOYSA-N 3-(2-iodophenyl)-2-[4-(2-methylphenyl)-3h-1,3-thiazol-2-ylidene]-3-oxopropanenitrile Chemical compound CC1=CC=CC=C1C(N1)=CSC1=C(C#N)C(=O)C1=CC=CC=C1I QOZUJMONBWCZBM-UHFFFAOYSA-N 0.000 description 1
- WZXRPDNMKGXBKU-UHFFFAOYSA-N 3-(2-methylphenyl)-2-(5-methyl-4-phenyl-3h-1,3-thiazol-2-ylidene)-3-oxopropanenitrile Chemical compound S1C(C)=C(C=2C=CC=CC=2)NC1=C(C#N)C(=O)C1=CC=CC=C1C WZXRPDNMKGXBKU-UHFFFAOYSA-N 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000726103 Atta Species 0.000 description 1
- NRCLXRFTTWSRAW-UHFFFAOYSA-N BrC1=C(NCS1)C1=CC=CC=C1 Chemical compound BrC1=C(NCS1)C1=CC=CC=C1 NRCLXRFTTWSRAW-UHFFFAOYSA-N 0.000 description 1
- CPXCGLHELGTARP-UHFFFAOYSA-N CC1=CC=CC=C1C1=CSC(=C(C=O)C#N)N1 Chemical compound CC1=CC=CC=C1C1=CSC(=C(C=O)C#N)N1 CPXCGLHELGTARP-UHFFFAOYSA-N 0.000 description 1
- 101100124609 Caenorhabditis elegans zyg-12 gene Proteins 0.000 description 1
- 241000255579 Ceratitis capitata Species 0.000 description 1
- 241000254173 Coleoptera Species 0.000 description 1
- 241000255925 Diptera Species 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 241000255777 Lepidoptera Species 0.000 description 1
- 235000019738 Limestone Nutrition 0.000 description 1
- NRWLBZAODDFNNT-UHFFFAOYSA-O N#CC(C(C(C=CC=C1)=C1Cl)=O)=C(NC=C1)[S+]1C1=CC=CS1 Chemical compound N#CC(C(C(C=CC=C1)=C1Cl)=O)=C(NC=C1)[S+]1C1=CC=CS1 NRWLBZAODDFNNT-UHFFFAOYSA-O 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
- 241000255588 Tephritidae Species 0.000 description 1
- FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
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- 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
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- 235000013339 cereals Nutrition 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- 229930016911 cinnamic acid Natural products 0.000 description 1
- 235000013985 cinnamic acid Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 1
- 239000007884 disintegrant Substances 0.000 description 1
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- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 description 1
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- 238000010438 heat treatment Methods 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
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- 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
- 239000006028 limestone Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 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 class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D277/00—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings
- C07D277/02—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings
- C07D277/20—Heterocyclic compounds containing 1,3-thiazole or hydrogenated 1,3-thiazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
-
- 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
- A01N43/74—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19792920183 DE2920183A1 (de) | 1979-05-17 | 1979-05-17 | Thiazolyliden-oxo-propionitrile, insektizide mittel enthaltend diese verbindungen sowie verfahren zu ihrer herstellung |
| DE2920183 | 1979-05-17 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| FI801379A7 FI801379A7 (fi) | 1980-11-18 |
| FI70889B FI70889B (fi) | 1986-07-18 |
| FI70889C true FI70889C (fi) | 1986-10-27 |
Family
ID=6071133
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| FI801379A FI70889C (fi) | 1979-05-17 | 1980-04-29 | Saosom insekticida medel anvaendbara tiazolyliden-oxo-propionitriler och foerfarande foer deras framstaellning |
Country Status (37)
| Country | Link |
|---|---|
| US (1) | US4297361A (cs) |
| JP (1) | JPS5925789B2 (cs) |
| AT (1) | AT366886B (cs) |
| AU (1) | AU531811B2 (cs) |
| BE (1) | BE883348A (cs) |
| BG (1) | BG34443A3 (cs) |
| BR (1) | BR8003059A (cs) |
| CA (1) | CA1136143A (cs) |
| CH (1) | CH644601A5 (cs) |
| CS (1) | CS216221B2 (cs) |
| DD (1) | DD150840A5 (cs) |
| DE (1) | DE2920183A1 (cs) |
| DK (1) | DK211380A (cs) |
| EG (1) | EG14276A (cs) |
| ES (1) | ES8107204A1 (cs) |
| FI (1) | FI70889C (cs) |
| FR (1) | FR2456737A1 (cs) |
| GB (1) | GB2051052B (cs) |
| GR (1) | GR67663B (cs) |
| HU (1) | HU187276B (cs) |
| IE (1) | IE49802B1 (cs) |
| IL (1) | IL60080A (cs) |
| IN (1) | IN154174B (cs) |
| IT (1) | IT1140847B (cs) |
| LU (1) | LU82457A1 (cs) |
| MA (1) | MA18847A1 (cs) |
| MX (1) | MX6405E (cs) |
| NL (1) | NL8001920A (cs) |
| NZ (1) | NZ193666A (cs) |
| PL (1) | PL121559B1 (cs) |
| PT (1) | PT71243A (cs) |
| RO (1) | RO80087A (cs) |
| SE (1) | SE8003465L (cs) |
| SU (1) | SU902665A3 (cs) |
| TR (1) | TR20541A (cs) |
| YU (1) | YU41208B (cs) |
| ZA (1) | ZA802923B (cs) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4626543A (en) * | 1985-02-01 | 1986-12-02 | Shell Oil Company | Insecticidal 2,6-difluorobenzoyl derivatives of 4-substituted-1,3-thiazole-2-acetonitriles |
| AU5514896A (en) * | 1995-04-27 | 1996-11-18 | Nissan Chemical Industries Ltd. | Oxopropionitrile derivatives and insect rest control agents |
| CA2252536C (en) | 1996-04-25 | 2010-04-06 | Nissan Chemical Industries, Ltd. | Ethylene derivatives and pesticides containing said derivatives |
| DE19851986A1 (de) * | 1998-11-11 | 2000-05-18 | Bayer Ag | Phenyl-substituierte zyklische Enaminone |
| WO2001047903A1 (fr) * | 1999-12-27 | 2001-07-05 | Nippon Soda Co., Ltd. | Composes de thiazolylcinnamonitrile, et insecticides et acaricides |
| WO2001068589A1 (fr) * | 2000-03-17 | 2001-09-20 | Nippon Soda Co.,Ltd. | Composes acrylonitrile et agents pesticides |
| JPWO2002088099A1 (ja) * | 2001-04-27 | 2004-08-19 | 日本曹達株式会社 | チアゾリルケイ皮酸ニトリル化合物および有害生物防除剤 |
| WO2003064401A1 (fr) * | 2002-01-29 | 2003-08-07 | Nippon Soda Co., Ltd. | Composes acrylonitriles et pesticides |
| USD702103S1 (en) * | 2012-04-12 | 2014-04-08 | Qaid Zohar Zakiuddin Shahpurwala | Padlock |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1192701A (en) * | 1968-03-22 | 1970-05-20 | Ici Ltd | Novel Thiazole Derivatives, the preparation thereof and Compositions containing the same |
| US3769040A (en) * | 1970-11-09 | 1973-10-30 | Int Flavors & Fragrances Inc | Substituted thiazoles in flavoring processes and products produced thereby |
| US3637707A (en) * | 1970-11-24 | 1972-01-25 | Pfizer | 2-(substituted) 2-thiazolines for the control of rice blast |
| DE2703542C2 (de) * | 1977-01-26 | 1985-09-26 | Schering AG, 1000 Berlin und 4709 Bergkamen | Thiazolylzimtsäurenitrile, Insektenbekämpfungsmittel enthaltend diese Verbindungen sowie Verfahren zu ihrer Herstellung |
| DE2801794A1 (de) * | 1978-01-17 | 1979-07-19 | Basf Ag | Verfahren zur herstellung von thiazolderivaten und neue thiazole |
-
1979
- 1979-05-17 DE DE19792920183 patent/DE2920183A1/de not_active Ceased
-
1980
- 1980-04-01 NL NL8001920A patent/NL8001920A/nl not_active Application Discontinuation
- 1980-04-23 SU SU802912755A patent/SU902665A3/ru active
- 1980-04-29 YU YU1163/80A patent/YU41208B/xx unknown
- 1980-04-29 FI FI801379A patent/FI70889C/fi not_active IP Right Cessation
- 1980-04-29 IN IN318/DEL/80A patent/IN154174B/en unknown
- 1980-05-05 CS CS803122A patent/CS216221B2/cs unknown
- 1980-05-06 TR TR20541A patent/TR20541A/xx unknown
- 1980-05-08 IT IT21877/80A patent/IT1140847B/it active
- 1980-05-08 SE SE8003465A patent/SE8003465L/xx not_active Application Discontinuation
- 1980-05-08 CH CH363180A patent/CH644601A5/de not_active IP Right Cessation
- 1980-05-09 NZ NZ193666A patent/NZ193666A/xx unknown
- 1980-05-09 BG BG047700A patent/BG34443A3/xx unknown
- 1980-05-12 GB GB8015671A patent/GB2051052B/en not_active Expired
- 1980-05-12 MX MX808808U patent/MX6405E/es unknown
- 1980-05-13 AU AU58339/80A patent/AU531811B2/en not_active Ceased
- 1980-05-14 ES ES491527A patent/ES8107204A1/es not_active Expired
- 1980-05-14 FR FR8010870A patent/FR2456737A1/fr active Granted
- 1980-05-14 PT PT71243A patent/PT71243A/pt unknown
- 1980-05-14 DK DK211380A patent/DK211380A/da not_active Application Discontinuation
- 1980-05-15 PL PL1980224257A patent/PL121559B1/pl unknown
- 1980-05-15 IL IL60080A patent/IL60080A/xx unknown
- 1980-05-15 DD DD80221139A patent/DD150840A5/de unknown
- 1980-05-15 GR GR61954A patent/GR67663B/el unknown
- 1980-05-16 AT AT0263680A patent/AT366886B/de not_active IP Right Cessation
- 1980-05-16 LU LU82457A patent/LU82457A1/de unknown
- 1980-05-16 BR BR8003059A patent/BR8003059A/pt unknown
- 1980-05-16 CA CA000352129A patent/CA1136143A/en not_active Expired
- 1980-05-16 ZA ZA00802923A patent/ZA802923B/xx unknown
- 1980-05-16 BE BE0/200654A patent/BE883348A/fr not_active IP Right Cessation
- 1980-05-16 HU HU801229A patent/HU187276B/hu unknown
- 1980-05-16 RO RO80101143A patent/RO80087A/ro unknown
- 1980-05-16 JP JP55065200A patent/JPS5925789B2/ja not_active Expired
- 1980-05-16 IE IE1018/80A patent/IE49802B1/en unknown
- 1980-05-17 MA MA19043A patent/MA18847A1/fr unknown
- 1980-05-17 EG EG303/80A patent/EG14276A/xx active
- 1980-05-19 US US06/151,109 patent/US4297361A/en not_active Expired - Lifetime
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM | Patent lapsed |
Owner name: SCHERING AKTIENGESELLSCHAFT |