NO802678L - Aryl(1-arylsulfonyl)vinylsulfoner. - Google Patents
Aryl(1-arylsulfonyl)vinylsulfoner.Info
- Publication number
- NO802678L NO802678L NO802678A NO802678A NO802678L NO 802678 L NO802678 L NO 802678L NO 802678 A NO802678 A NO 802678A NO 802678 A NO802678 A NO 802678A NO 802678 L NO802678 L NO 802678L
- Authority
- NO
- Norway
- Prior art keywords
- mol
- solution
- hydrogen
- phenyl
- compound according
- Prior art date
Links
- AFOSIXZFDONLBT-UHFFFAOYSA-N divinyl sulfone Chemical compound C=CS(=O)(=O)C=C AFOSIXZFDONLBT-UHFFFAOYSA-N 0.000 title 1
- -1 m-nitrophenyl Chemical group 0.000 claims description 25
- 150000001875 compounds Chemical class 0.000 claims description 22
- 229910052739 hydrogen Inorganic materials 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 230000003641 microbiacidal effect Effects 0.000 claims description 13
- 229940124561 microbicide Drugs 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 13
- 229910052736 halogen Inorganic materials 0.000 claims description 10
- 150000002367 halogens Chemical class 0.000 claims description 10
- 238000000034 method Methods 0.000 claims description 10
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- HZVOZRGWRWCICA-UHFFFAOYSA-N methanediyl Chemical group [CH2] HZVOZRGWRWCICA-UHFFFAOYSA-N 0.000 claims description 6
- 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 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- 239000002855 microbicide agent Substances 0.000 claims description 3
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
- 229910052794 bromium Inorganic materials 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 4
- 125000004970 halomethyl group Chemical group 0.000 claims 3
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims 3
- 150000002431 hydrogen Chemical group 0.000 claims 2
- 229910052757 nitrogen Inorganic materials 0.000 claims 2
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 claims 1
- 239000000460 chlorine Substances 0.000 description 38
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 33
- 238000002360 preparation method Methods 0.000 description 29
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 28
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 27
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 24
- 238000002844 melting Methods 0.000 description 23
- 230000008018 melting Effects 0.000 description 23
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 20
- 238000001704 evaporation Methods 0.000 description 19
- 230000008020 evaporation Effects 0.000 description 19
- 239000002904 solvent Substances 0.000 description 19
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 15
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 12
- 238000001953 recrystallisation Methods 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 229960000583 acetic acid Drugs 0.000 description 11
- 239000000203 mixture Substances 0.000 description 11
- 238000001914 filtration Methods 0.000 description 10
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 10
- 239000012043 crude product Substances 0.000 description 9
- 239000000706 filtrate Substances 0.000 description 9
- 239000012362 glacial acetic acid Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- ILWRPSCZWQJDMK-UHFFFAOYSA-N triethylazanium;chloride Chemical compound Cl.CCN(CC)CC ILWRPSCZWQJDMK-UHFFFAOYSA-N 0.000 description 9
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 8
- 239000011541 reaction mixture Substances 0.000 description 8
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 6
- 239000000839 emulsion Substances 0.000 description 6
- JWUKZUIGOJBEPC-UHFFFAOYSA-N phenyl thiohypochlorite Chemical compound ClSC1=CC=CC=C1 JWUKZUIGOJBEPC-UHFFFAOYSA-N 0.000 description 6
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 5
- 239000013078 crystal Substances 0.000 description 5
- UJTPZISIAWDGFF-UHFFFAOYSA-N ethenylsulfonylbenzene Chemical compound C=CS(=O)(=O)C1=CC=CC=C1 UJTPZISIAWDGFF-UHFFFAOYSA-N 0.000 description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
- 239000003208 petroleum Substances 0.000 description 5
- STDOUHHCZSZDME-UHFFFAOYSA-N (4-bromophenyl) thiohypochlorite Chemical compound ClSC1=CC=C(Br)C=C1 STDOUHHCZSZDME-UHFFFAOYSA-N 0.000 description 4
- IBJGVAOFRSKZPY-UHFFFAOYSA-N 1-chloro-4-ethenylsulfonylbenzene Chemical compound ClC1=CC=C(S(=O)(=O)C=C)C=C1 IBJGVAOFRSKZPY-UHFFFAOYSA-N 0.000 description 4
- VZQFRPMWVXCURA-UHFFFAOYSA-N 1-ethenylsulfonyl-4-methylbenzene Chemical compound CC1=CC=C(S(=O)(=O)C=C)C=C1 VZQFRPMWVXCURA-UHFFFAOYSA-N 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 4
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
- QVDYYQXUNAQSNI-UHFFFAOYSA-N ethyl acetate;pentane Chemical compound CCCCC.CCOC(C)=O QVDYYQXUNAQSNI-UHFFFAOYSA-N 0.000 description 4
- AOJFQRQNPXYVLM-UHFFFAOYSA-N pyridin-1-ium;chloride Chemical compound [Cl-].C1=CC=[NH+]C=C1 AOJFQRQNPXYVLM-UHFFFAOYSA-N 0.000 description 4
- GBIYAVWBYTZRNJ-UHFFFAOYSA-N (3-nitrophenyl) thiohypochlorite Chemical compound [O-][N+](=O)C1=CC=CC(SCl)=C1 GBIYAVWBYTZRNJ-UHFFFAOYSA-N 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- CNJPYZBIFBJWFS-UHFFFAOYSA-N 1-ethenylsulfonyl-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(S(=O)(=O)C=C)=C1 CNJPYZBIFBJWFS-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 3
- ZAFDTQJIAOZBAA-UHFFFAOYSA-N (3-methylphenyl) thiohypochlorite Chemical compound CC1=CC=CC(SCl)=C1 ZAFDTQJIAOZBAA-UHFFFAOYSA-N 0.000 description 2
- QAASGGHXTJRDLJ-UHFFFAOYSA-N (4-tert-butylphenyl) thiohypochlorite Chemical compound CC(C)(C)C1=CC=C(SCl)C=C1 QAASGGHXTJRDLJ-UHFFFAOYSA-N 0.000 description 2
- DAKKGNISJUIYLF-UHFFFAOYSA-N 1-[1-(benzenesulfonyl)-2-chloroethyl]sulfanyl-4-bromobenzene Chemical compound C=1C=CC=CC=1S(=O)(=O)C(CCl)SC1=CC=C(Br)C=C1 DAKKGNISJUIYLF-UHFFFAOYSA-N 0.000 description 2
- ZRGLIYSRLRPQDF-UHFFFAOYSA-N 1-[1-(benzenesulfonyl)-2-chloroethyl]sulfanyl-4-tert-butylbenzene Chemical compound C1=CC(C(C)(C)C)=CC=C1SC(CCl)S(=O)(=O)C1=CC=CC=C1 ZRGLIYSRLRPQDF-UHFFFAOYSA-N 0.000 description 2
- VNSXYYAVZSULCZ-UHFFFAOYSA-N 1-bromo-4-[2-chloro-1-(4-chlorophenyl)sulfonylethyl]sulfanylbenzene Chemical compound C=1C=C(Cl)C=CC=1S(=O)(=O)C(CCl)SC1=CC=C(Br)C=C1 VNSXYYAVZSULCZ-UHFFFAOYSA-N 0.000 description 2
- GRMNNUKUDFDMPB-UHFFFAOYSA-N 1-chloro-4-(2-chloro-1-phenylsulfanylethyl)sulfonylbenzene Chemical compound C=1C=C(Cl)C=CC=1S(=O)(=O)C(CCl)SC1=CC=CC=C1 GRMNNUKUDFDMPB-UHFFFAOYSA-N 0.000 description 2
- XAYJWVMHRNYQOX-UHFFFAOYSA-N 1-tert-butyl-4-(2-chloro-1-phenylsulfanylethyl)sulfonylbenzene Chemical compound C1=CC(C(C)(C)C)=CC=C1S(=O)(=O)C(CCl)SC1=CC=CC=C1 XAYJWVMHRNYQOX-UHFFFAOYSA-N 0.000 description 2
- SVPZEQNJJDFQGK-UHFFFAOYSA-N 1-tert-butyl-4-[2-chloro-1-(4-chlorophenyl)sulfonylethyl]sulfanylbenzene Chemical compound C1=CC(C(C)(C)C)=CC=C1SC(CCl)S(=O)(=O)C1=CC=C(Cl)C=C1 SVPZEQNJJDFQGK-UHFFFAOYSA-N 0.000 description 2
- 241001558165 Alternaria sp. Species 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 241001149959 Fusarium sp. Species 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- BAVYZALUXZFZLV-UHFFFAOYSA-N Methylamine Chemical compound NC BAVYZALUXZFZLV-UHFFFAOYSA-N 0.000 description 2
- 241001385948 Pythium sp. Species 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- FWMUJAIKEJWSSY-UHFFFAOYSA-N sulfur dichloride Chemical compound ClSCl FWMUJAIKEJWSSY-UHFFFAOYSA-N 0.000 description 2
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 2
- 229920002554 vinyl polymer Polymers 0.000 description 2
- WVTOJNFZIVWNIY-UHFFFAOYSA-N (4-chlorophenyl) thiohypochlorite Chemical compound ClSC1=CC=C(Cl)C=C1 WVTOJNFZIVWNIY-UHFFFAOYSA-N 0.000 description 1
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- CTDPQIDVQZAGIH-UHFFFAOYSA-N 1-(2-chloro-1-phenylsulfanylethyl)sulfonyl-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(S(=O)(=O)C(CCl)SC=2C=CC=CC=2)=C1 CTDPQIDVQZAGIH-UHFFFAOYSA-N 0.000 description 1
- VDDLMNHLOLCHRE-UHFFFAOYSA-N 1-[1-(4-bromophenyl)sulfanyl-2-chloroethyl]sulfonyl-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(S(=O)(=O)C(CCl)SC=2C=CC(Br)=CC=2)=C1 VDDLMNHLOLCHRE-UHFFFAOYSA-N 0.000 description 1
- VBEWLPKASHTJNN-UHFFFAOYSA-N 1-[1-(4-bromophenyl)sulfanyl-2-chloroethyl]sulfonyl-4-methylbenzene Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(CCl)SC1=CC=C(Br)C=C1 VBEWLPKASHTJNN-UHFFFAOYSA-N 0.000 description 1
- TUWHXXBKLDBSRJ-UHFFFAOYSA-N 1-[1-(4-bromophenyl)sulfanylethenylsulfonyl]-3-nitrobenzene Chemical compound [O-][N+](=O)C1=CC=CC(S(=O)(=O)C(=C)SC=2C=CC(Br)=CC=2)=C1 TUWHXXBKLDBSRJ-UHFFFAOYSA-N 0.000 description 1
- IAJALEFQCZTQDM-UHFFFAOYSA-N 1-[1-(benzenesulfonyl)-2-chloroethyl]sulfanyl-4-chlorobenzene Chemical compound C=1C=CC=CC=1S(=O)(=O)C(CCl)SC1=CC=C(Cl)C=C1 IAJALEFQCZTQDM-UHFFFAOYSA-N 0.000 description 1
- AFGXNIPKFJITGH-UHFFFAOYSA-N 1-bromo-4-[1-(4-chlorophenyl)sulfonylethenylsulfanyl]benzene Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C(=C)SC1=CC=C(Br)C=C1 AFGXNIPKFJITGH-UHFFFAOYSA-N 0.000 description 1
- MRASNHJAIDLHAW-UHFFFAOYSA-N 1-chloro-4-(1-phenylsulfanylethenylsulfonyl)benzene Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C(=C)SC1=CC=CC=C1 MRASNHJAIDLHAW-UHFFFAOYSA-N 0.000 description 1
- ODOFDWDUSSFUMN-UHFFFAOYSA-N 1-nitro-3-[(3-nitrophenyl)disulfanyl]benzene Chemical compound [O-][N+](=O)C1=CC=CC(SSC=2C=C(C=CC=2)[N+]([O-])=O)=C1 ODOFDWDUSSFUMN-UHFFFAOYSA-N 0.000 description 1
- ZVPOBQOXHBZJJI-UHFFFAOYSA-N 1-tert-butyl-4-[1-(4-chlorophenyl)sulfonylethenylsulfanyl]benzene Chemical compound C1=CC(C(C)(C)C)=CC=C1SC(=C)S(=O)(=O)C1=CC=C(Cl)C=C1 ZVPOBQOXHBZJJI-UHFFFAOYSA-N 0.000 description 1
- XUCGDKWYZOHBKB-UHFFFAOYSA-N 1-tert-butyl-4-ethenylsulfonylbenzene Chemical compound CC(C)(C)C1=CC=C(S(=O)(=O)C=C)C=C1 XUCGDKWYZOHBKB-UHFFFAOYSA-N 0.000 description 1
- NAZFLTXEUHEMQU-UHFFFAOYSA-N 2-bromo-5-[4-bromo-6-chloro-1-(3-nitrophenyl)sulfonylcyclohexa-2,4-dien-1-yl]sulfanyl-6-chloro-5-(3-nitrophenyl)sulfonylcyclohexa-1,3-diene Chemical compound [O-][N+](=O)C1=CC=CC(S(=O)(=O)C2(SC3(C(C=C(Br)C=C3)Cl)S(=O)(=O)C=3C=C(C=CC=3)[N+]([O-])=O)C(C=C(Br)C=C2)Cl)=C1 NAZFLTXEUHEMQU-UHFFFAOYSA-N 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 1
- XGEJPZWLVJMNCR-UHFFFAOYSA-N OC(O)=O.Cl.Cl.Cl.Cl Chemical compound OC(O)=O.Cl.Cl.Cl.Cl XGEJPZWLVJMNCR-UHFFFAOYSA-N 0.000 description 1
- GMPDOIGGGXSAPL-UHFFFAOYSA-N Phenyl vinyl sulfide Chemical compound C=CSC1=CC=CC=C1 GMPDOIGGGXSAPL-UHFFFAOYSA-N 0.000 description 1
- 241001361634 Rhizoctonia Species 0.000 description 1
- 241000684075 Rhizoctonia sp. Species 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- UCKMPCXJQFINFW-UHFFFAOYSA-N Sulphide Chemical compound [S-2] UCKMPCXJQFINFW-UHFFFAOYSA-N 0.000 description 1
- RKDFVVULDZJBNX-UHFFFAOYSA-N [1-[1-(benzenesulfonyl)-2-chloroethyl]sulfanyl-2-chloroethyl]sulfonylbenzene Chemical compound C=1C=CC=CC=1S(=O)(=O)C(CCl)SC(CCl)S(=O)(=O)C1=CC=CC=C1 RKDFVVULDZJBNX-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000010549 co-Evaporation Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000006704 dehydrohalogenation reaction Methods 0.000 description 1
- SWXVUIWOUIDPGS-UHFFFAOYSA-N diacetone alcohol Chemical compound CC(=O)CC(C)(C)O SWXVUIWOUIDPGS-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- JHGHTBSOZYDUJC-UHFFFAOYSA-N ethenylsulfonylcyclohexane Chemical compound C=CS(=O)(=O)C1CCCCC1 JHGHTBSOZYDUJC-UHFFFAOYSA-N 0.000 description 1
- 125000000219 ethylidene group Chemical group [H]C(=[*])C([H])([H])[H] 0.000 description 1
- IFYLVUHLOOCYBG-UHFFFAOYSA-N eticyclidine Chemical compound C=1C=CC=CC=1C1(NCC)CCCCC1 IFYLVUHLOOCYBG-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- 125000000843 phenylene group Chemical group C1(=C(C=CC=C1)*)* 0.000 description 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 238000001291 vacuum drying Methods 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
Classifications
-
- 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
- A01N41/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom
- A01N41/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a sulfur atom bound to a hetero atom containing a sulfur-to-oxygen double bond
- A01N41/10—Sulfones; Sulfoxides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C321/00—Thiols, sulfides, hydropolysulfides or polysulfides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Polyoxymethylene Polymers And Polymers With Carbon-To-Carbon Bonds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US06/074,271 US4335142A (en) | 1979-09-11 | 1979-09-11 | Aryl (1-arylsulfonyl) vinyl sulfones |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NO802678L true NO802678L (no) | 1981-03-12 |
Family
ID=22118690
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO802678A NO802678L (no) | 1979-09-11 | 1980-09-10 | Aryl(1-arylsulfonyl)vinylsulfoner. |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US4335142A (enExample) |
| EP (1) | EP0025339B1 (enExample) |
| JP (1) | JPS5699455A (enExample) |
| CA (1) | CA1123459A (enExample) |
| DE (1) | DE3068037D1 (enExample) |
| GR (1) | GR69981B (enExample) |
| NO (1) | NO802678L (enExample) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL342291A1 (en) * | 1998-02-09 | 2001-06-04 | Sumitomo Chemical Co | Method of obtaining aryl vinyl sulphone solution |
| US6232503B1 (en) | 1999-03-19 | 2001-05-15 | Lonza Inc. | Alkynyl aryl sulfones |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3242041A (en) * | 1964-07-21 | 1966-03-22 | Chemagro Corp | Method for killing fungi with vinyl sulfones |
| US3629438A (en) * | 1969-01-23 | 1971-12-21 | Uniroyal Inc | Benzothiophene-1 1-dioxide derivatives as fungicides and bactericides |
| US3682212A (en) * | 1970-06-01 | 1972-08-08 | Weir Magic Pit Corp | Method of manufacturing wood-siding panels |
| US4031247A (en) * | 1976-02-12 | 1977-06-21 | Chevron Research Company | Fungicidal vinyl 2-substituted-thiovinyl sulfones |
-
1979
- 1979-09-11 US US06/074,271 patent/US4335142A/en not_active Expired - Lifetime
-
1980
- 1980-01-15 CA CA343,744A patent/CA1123459A/en not_active Expired
- 1980-09-03 EP EP80303077A patent/EP0025339B1/en not_active Expired
- 1980-09-03 DE DE8080303077T patent/DE3068037D1/de not_active Expired
- 1980-09-04 GR GR62808A patent/GR69981B/el unknown
- 1980-09-10 NO NO802678A patent/NO802678L/no unknown
- 1980-09-11 JP JP12662480A patent/JPS5699455A/ja active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| EP0025339B1 (en) | 1984-05-30 |
| GR69981B (enExample) | 1982-07-22 |
| US4335142A (en) | 1982-06-15 |
| CA1123459A (en) | 1982-05-11 |
| DE3068037D1 (en) | 1984-07-05 |
| EP0025339A1 (en) | 1981-03-18 |
| JPS5699455A (en) | 1981-08-10 |
| JPS5736276B2 (enExample) | 1982-08-03 |
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