BG63255B1 - 1,4-диарил-2-флуоро-2-бутенови инсектицидни и акарицидни средства - Google Patents
1,4-диарил-2-флуоро-2-бутенови инсектицидни и акарицидни средства Download PDFInfo
- Publication number
- BG63255B1 BG63255B1 BG101535A BG10153597A BG63255B1 BG 63255 B1 BG63255 B1 BG 63255B1 BG 101535 A BG101535 A BG 101535A BG 10153597 A BG10153597 A BG 10153597A BG 63255 B1 BG63255 B1 BG 63255B1
- Authority
- BG
- Bulgaria
- Prior art keywords
- alkyl
- fluoro
- haloalkyl
- optionally substituted
- combination
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title description 31
- 230000000895 acaricidal effect Effects 0.000 title description 5
- 239000002917 insecticide Substances 0.000 title description 4
- 238000009472 formulation Methods 0.000 title description 3
- 238000000034 method Methods 0.000 claims abstract description 37
- 241000238631 Hexapoda Species 0.000 claims abstract description 12
- -1 C 1 -C 4 alkyl Chemical group 0.000 claims description 129
- 125000005843 halogen group Chemical group 0.000 claims description 93
- 150000001875 compounds Chemical class 0.000 claims description 84
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims description 73
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 54
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 45
- 229910052739 hydrogen Inorganic materials 0.000 claims description 37
- 239000001257 hydrogen Substances 0.000 claims description 37
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 36
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 22
- LVZWSLJZHVFIQJ-UHFFFAOYSA-N Cyclopropane Chemical compound C1CC1 LVZWSLJZHVFIQJ-UHFFFAOYSA-N 0.000 claims description 20
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 19
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims description 19
- 238000002360 preparation method Methods 0.000 claims description 19
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 16
- 229910052799 carbon Inorganic materials 0.000 claims description 16
- 125000004432 carbon atom Chemical group C* 0.000 claims description 15
- 150000002431 hydrogen Chemical class 0.000 claims description 14
- 241000238876 Acari Species 0.000 claims description 12
- 229910052794 bromium Inorganic materials 0.000 claims description 12
- 239000000460 chlorine Substances 0.000 claims description 12
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 11
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims description 11
- 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 claims description 10
- 125000005842 heteroatom Chemical group 0.000 claims description 10
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 9
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 9
- RYPKRALMXUUNKS-UHFFFAOYSA-N 2-Hexene Natural products CCCC=CC RYPKRALMXUUNKS-UHFFFAOYSA-N 0.000 claims description 8
- 229910052801 chlorine Inorganic materials 0.000 claims description 8
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 8
- KDLHZDBZIXYQEI-UHFFFAOYSA-N Palladium Chemical compound [Pd] KDLHZDBZIXYQEI-UHFFFAOYSA-N 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- ZEGMZHCBTQZHEY-UHFFFAOYSA-N 4-[4-(4-chlorophenyl)-3-fluoro-4-methylpent-2-enyl]-1-fluoro-2-phenoxybenzene Chemical compound C=1C=C(Cl)C=CC=1C(C)(C)C(F)=CCC(C=1)=CC=C(F)C=1OC1=CC=CC=C1 ZEGMZHCBTQZHEY-UHFFFAOYSA-N 0.000 claims description 6
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 6
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 6
- 239000011777 magnesium Substances 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 239000002689 soil Substances 0.000 claims description 6
- ATOQCDOIWWGTFN-UHFFFAOYSA-N 4-[3-[1-(4-chlorophenyl)cyclopropyl]-3-fluoroprop-2-enyl]-1-fluoro-2-phenoxybenzene Chemical compound C1CC1(C=1C=CC(Cl)=CC=1)C(F)=CCC(C=1)=CC=C(F)C=1OC1=CC=CC=C1 ATOQCDOIWWGTFN-UHFFFAOYSA-N 0.000 claims description 5
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 5
- 150000008366 benzophenones Chemical class 0.000 claims description 5
- 125000004368 propenyl group Chemical group C(=CC)* 0.000 claims description 5
- WDCSCGIZSMVNSU-UHFFFAOYSA-N 4-[4-(4-chlorophenyl)-4-cyclopropyl-3-fluorobut-2-enyl]-1-fluoro-2-phenoxybenzene Chemical compound C1CC1C(C=1C=CC(Cl)=CC=1)C(F)=CCC(C=1)=CC=C(F)C=1OC1=CC=CC=C1 WDCSCGIZSMVNSU-UHFFFAOYSA-N 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 4
- 241000607479 Yersinia pestis Species 0.000 claims description 4
- 125000006268 biphenyl-3-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C([H])C(*)=C([H])C([H])=C1[H] 0.000 claims description 4
- 229910052749 magnesium Inorganic materials 0.000 claims description 4
- 230000000361 pesticidal effect Effects 0.000 claims description 4
- 125000006677 (C1-C3) haloalkoxy group Chemical group 0.000 claims description 3
- VDNCRLDCVRUNFE-UHFFFAOYSA-N 4-[4-(4-ethoxyphenyl)-3-fluoro-5-methylhex-2-enyl]-1-fluoro-2-phenoxybenzene Chemical compound C1=CC(OCC)=CC=C1C(C(C)C)C(F)=CCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 VDNCRLDCVRUNFE-UHFFFAOYSA-N 0.000 claims description 3
- ZQBLOMHMJDCYDH-UHFFFAOYSA-N 4-[4-cyclopropyl-3-fluoro-4-(4-fluorophenyl)but-2-enyl]-1-fluoro-2-phenoxybenzene Chemical compound C1CC1C(C=1C=CC(F)=CC=1)C(F)=CCC(C=1)=CC=C(F)C=1OC1=CC=CC=C1 ZQBLOMHMJDCYDH-UHFFFAOYSA-N 0.000 claims description 3
- ZOFJNSUSZKZYBI-UHFFFAOYSA-N 4-[4-cyclopropyl-4-(4-ethoxyphenyl)-3-fluorobut-2-enyl]-1-fluoro-2-phenoxybenzene Chemical compound C1=CC(OCC)=CC=C1C(C(F)=CCC=1C=C(OC=2C=CC=CC=2)C(F)=CC=1)C1CC1 ZOFJNSUSZKZYBI-UHFFFAOYSA-N 0.000 claims description 3
- 239000000642 acaricide Substances 0.000 claims description 3
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 3
- 150000001993 dienes Chemical class 0.000 claims description 3
- VYYZHLFDYDAMAR-UHFFFAOYSA-N 4-[4-(4-chlorophenyl)-3-fluoro-5-methylhex-2-enyl]-1-fluoro-2-phenoxybenzene Chemical compound C=1C=C(Cl)C=CC=1C(C(C)C)C(F)=CCC(C=1)=CC=C(F)C=1OC1=CC=CC=C1 VYYZHLFDYDAMAR-UHFFFAOYSA-N 0.000 claims description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 2
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 claims description 2
- 239000004327 boric acid Substances 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 235000013305 food Nutrition 0.000 claims description 2
- 229910052763 palladium Inorganic materials 0.000 claims description 2
- ZUOUZKKEUPVFJK-UHFFFAOYSA-N diphenyl Chemical group C1=CC=CC=C1C1=CC=CC=C1 ZUOUZKKEUPVFJK-UHFFFAOYSA-N 0.000 claims 10
- 125000001637 1-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C(*)=C([H])C([H])=C([H])C2=C1[H] 0.000 claims 8
- 125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims 8
- 239000004305 biphenyl Chemical group 0.000 claims 5
- 235000010290 biphenyl Nutrition 0.000 claims 5
- 230000003287 optical effect Effects 0.000 claims 5
- CZZYITDELCSZES-UHFFFAOYSA-N diphenylmethane Chemical group C=1C=CC=CC=1CC1=CC=CC=C1 CZZYITDELCSZES-UHFFFAOYSA-N 0.000 claims 4
- XQBORONAEOLVOI-UHFFFAOYSA-N 1-chloro-4-[1-cyclopropyl-2-fluoro-4-[3-(4-fluorophenoxy)phenyl]but-2-enyl]benzene Chemical compound C1CC1C(C=1C=CC(Cl)=CC=1)C(F)=CCC(C=1)=CC=CC=1OC1=CC=C(F)C=C1 XQBORONAEOLVOI-UHFFFAOYSA-N 0.000 claims 2
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 claims 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 claims 1
- FLZSFRMOTOGRCV-UHFFFAOYSA-N 1-chloro-4-[3-fluoro-2-methyl-5-(3-phenoxyphenyl)pent-3-en-2-yl]benzene Chemical compound C=1C=C(Cl)C=CC=1C(C)(C)C(F)=CCC(C=1)=CC=CC=1OC1=CC=CC=C1 FLZSFRMOTOGRCV-UHFFFAOYSA-N 0.000 claims 1
- JHOYSXNCALOZDS-UHFFFAOYSA-N 1-ethoxy-4-[4-fluoro-2-methyl-6-(3-phenoxyphenyl)hex-4-en-3-yl]benzene Chemical compound C1=CC(OCC)=CC=C1C(C(C)C)C(F)=CCC1=CC=CC(OC=2C=CC=CC=2)=C1 JHOYSXNCALOZDS-UHFFFAOYSA-N 0.000 claims 1
- DGVCIELPWQJSAH-UHFFFAOYSA-N 1-ethoxy-4-[4-fluoro-6-[3-(4-fluorophenoxy)phenyl]-2-methylhex-4-en-3-yl]benzene Chemical compound C1=CC(OCC)=CC=C1C(C(C)C)C(F)=CCC1=CC=CC(OC=2C=CC(F)=CC=2)=C1 DGVCIELPWQJSAH-UHFFFAOYSA-N 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 238000009395 breeding Methods 0.000 claims 1
- 230000001488 breeding effect Effects 0.000 claims 1
- 125000004438 haloalkoxy group Chemical group 0.000 claims 1
- 125000001188 haloalkyl group Chemical group 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 239000003586 protic polar solvent Substances 0.000 claims 1
- 241001474033 Acar Species 0.000 abstract 1
- 239000000575 pesticide Substances 0.000 abstract 1
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 60
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 47
- 239000000243 solution Substances 0.000 description 44
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 40
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 34
- 238000006243 chemical reaction Methods 0.000 description 27
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 22
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 239000003921 oil Substances 0.000 description 15
- 241000196324 Embryophyta Species 0.000 description 14
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 14
- 239000011541 reaction mixture Substances 0.000 description 14
- 239000000284 extract Substances 0.000 description 13
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 12
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 12
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 12
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 12
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 11
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 9
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 9
- 239000002585 base Substances 0.000 description 9
- MZRVEZGGRBJDDB-UHFFFAOYSA-N N-Butyllithium Chemical compound [Li]CCCC MZRVEZGGRBJDDB-UHFFFAOYSA-N 0.000 description 8
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 239000000741 silica gel Substances 0.000 description 8
- 229910002027 silica gel Inorganic materials 0.000 description 8
- 239000012230 colorless oil Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 239000007787 solid Substances 0.000 description 6
- 239000012085 test solution Substances 0.000 description 6
- 241001454293 Tetranychus urticae Species 0.000 description 5
- XJHCXCQVJFPJIK-UHFFFAOYSA-M caesium fluoride Chemical compound [F-].[Cs+] XJHCXCQVJFPJIK-UHFFFAOYSA-M 0.000 description 5
- 238000011161 development Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 238000012360 testing method Methods 0.000 description 5
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- SIPUZPBQZHNSDW-UHFFFAOYSA-N bis(2-methylpropyl)aluminum Chemical compound CC(C)C[Al]CC(C)C SIPUZPBQZHNSDW-UHFFFAOYSA-N 0.000 description 4
- 239000003638 chemical reducing agent Substances 0.000 description 4
- 239000000543 intermediate Substances 0.000 description 4
- 239000012280 lithium aluminium hydride Substances 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- HJUGFYREWKUQJT-UHFFFAOYSA-N tetrabromomethane Chemical compound BrC(Br)(Br)Br HJUGFYREWKUQJT-UHFFFAOYSA-N 0.000 description 4
- IYQSVYUQWPQOAW-UHFFFAOYSA-N 1-chloro-4-(1-cyclopropyl-2-methoxyethenyl)benzene Chemical compound C=1C=C(Cl)C=CC=1C(=COC)C1CC1 IYQSVYUQWPQOAW-UHFFFAOYSA-N 0.000 description 3
- GVNVAWHJIKLAGL-UHFFFAOYSA-N 2-(cyclohexen-1-yl)cyclohexan-1-one Chemical compound O=C1CCCCC1C1=CCCCC1 GVNVAWHJIKLAGL-UHFFFAOYSA-N 0.000 description 3
- ZUCCKSAKSZVZDF-UHFFFAOYSA-N 4-(4-chlorophenyl)-3-fluoro-4-methylpent-2-en-1-ol Chemical compound OCC=C(F)C(C)(C)C1=CC=C(Cl)C=C1 ZUCCKSAKSZVZDF-UHFFFAOYSA-N 0.000 description 3
- IXBKJJBPCGWIPY-UHFFFAOYSA-N 4-(4-chlorophenyl)-4-methylpent-2-enal Chemical compound O=CC=CC(C)(C)C1=CC=C(Cl)C=C1 IXBKJJBPCGWIPY-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- 241001124076 Aphididae Species 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 3
- 101150065749 Churc1 gene Proteins 0.000 description 3
- 239000005909 Kieselgur Substances 0.000 description 3
- 238000005481 NMR spectroscopy Methods 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- 102100038239 Protein Churchill Human genes 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- 240000008042 Zea mays Species 0.000 description 3
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 3
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 3
- 239000004480 active ingredient Substances 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- JPBIBQAYXLZJBV-UHFFFAOYSA-N bis[1-(4-chlorophenyl)cyclopropyl]methanone Chemical compound C1=CC(Cl)=CC=C1C1(C(=O)C2(CC2)C=2C=CC(Cl)=CC=2)CC1 JPBIBQAYXLZJBV-UHFFFAOYSA-N 0.000 description 3
- 235000011089 carbon dioxide Nutrition 0.000 description 3
- 229950005499 carbon tetrachloride Drugs 0.000 description 3
- UMNKXPULIDJLSU-UHFFFAOYSA-N dichlorofluoromethane Chemical compound FC(Cl)Cl UMNKXPULIDJLSU-UHFFFAOYSA-N 0.000 description 3
- 229940099364 dichlorofluoromethane Drugs 0.000 description 3
- 238000002474 experimental method Methods 0.000 description 3
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 3
- 125000002541 furyl group Chemical group 0.000 description 3
- 229910052740 iodine Inorganic materials 0.000 description 3
- 235000009973 maize Nutrition 0.000 description 3
- 229910000104 sodium hydride Inorganic materials 0.000 description 3
- 239000012312 sodium hydride Substances 0.000 description 3
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 3
- 239000011701 zinc Substances 0.000 description 3
- UKSZBOKPHAQOMP-SVLSSHOZSA-N (1e,4e)-1,5-diphenylpenta-1,4-dien-3-one;palladium Chemical compound [Pd].C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1.C=1C=CC=CC=1\C=C\C(=O)\C=C\C1=CC=CC=C1 UKSZBOKPHAQOMP-SVLSSHOZSA-N 0.000 description 2
- OQENDCZUYYJXME-UHFFFAOYSA-M (4-fluoro-3-phenoxyphenyl)methyl-triphenylphosphanium;bromide Chemical compound [Br-].C1=C(OC=2C=CC=CC=2)C(F)=CC=C1C[P+](C=1C=CC=CC=1)(C=1C=CC=CC=1)C1=CC=CC=C1 OQENDCZUYYJXME-UHFFFAOYSA-M 0.000 description 2
- GHBKCPRDHLITSE-SNAWJCMRSA-N (e)-5-methylhex-2-ene Chemical compound C\C=C\CC(C)C GHBKCPRDHLITSE-SNAWJCMRSA-N 0.000 description 2
- GSKYOTMUMFSKAS-UHFFFAOYSA-N 1-(1-cyclopropyl-2-methoxyethenyl)-4-fluorobenzene Chemical compound C=1C=C(F)C=CC=1C(=COC)C1CC1 GSKYOTMUMFSKAS-UHFFFAOYSA-N 0.000 description 2
- HEGXENQCLACJQG-UHFFFAOYSA-N 1-(4-chlorophenyl)cyclopropane-1-carbaldehyde Chemical compound C1=CC(Cl)=CC=C1C1(C=O)CC1 HEGXENQCLACJQG-UHFFFAOYSA-N 0.000 description 2
- RLKGYKDPDZCNLH-UHFFFAOYSA-N 1-(5-bromo-3-fluoro-2-methylpent-3-en-2-yl)-4-chlorobenzene Chemical compound BrCC=C(F)C(C)(C)C1=CC=C(Cl)C=C1 RLKGYKDPDZCNLH-UHFFFAOYSA-N 0.000 description 2
- QHNFCAGAHWGYNM-UHFFFAOYSA-N 1-chloro-4-[1-(2,2-dibromoethenyl)cyclopropyl]benzene Chemical compound C1=CC(Cl)=CC=C1C1(C=C(Br)Br)CC1 QHNFCAGAHWGYNM-UHFFFAOYSA-N 0.000 description 2
- XEZNGIUYQVAUSS-UHFFFAOYSA-N 18-crown-6 Chemical compound C1COCCOCCOCCOCCOCCO1 XEZNGIUYQVAUSS-UHFFFAOYSA-N 0.000 description 2
- YNXOMDRPWQMDQL-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-methylpropanal Chemical compound O=CC(C)(C)C1=CC=C(Cl)C=C1 YNXOMDRPWQMDQL-UHFFFAOYSA-N 0.000 description 2
- GQOLYABRQATDOI-UHFFFAOYSA-N 2-(4-chlorophenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)C1=CC=C(Cl)C=C1 GQOLYABRQATDOI-UHFFFAOYSA-N 0.000 description 2
- ASZZHBXPMOVHCU-UHFFFAOYSA-N 3,9-diazaspiro[5.5]undecane-2,4-dione Chemical compound C1C(=O)NC(=O)CC11CCNCC1 ASZZHBXPMOVHCU-UHFFFAOYSA-N 0.000 description 2
- ORJUZONMHNWKBS-UHFFFAOYSA-N 3-(4-chlorophenyl)-3-cyclopropyl-2-fluoroprop-2-en-1-ol Chemical compound C=1C=C(Cl)C=CC=1C(=C(F)CO)C1CC1 ORJUZONMHNWKBS-UHFFFAOYSA-N 0.000 description 2
- LINCLFQLZHCRHE-UHFFFAOYSA-N 4-[4-(4-chlorophenyl)-4-cyclopropyl-3-fluorobuta-1,3-dienyl]-1-fluoro-2-phenoxybenzene Chemical compound C1CC1C(C=1C=CC(Cl)=CC=1)=C(F)C=CC(C=1)=CC=C(F)C=1OC1=CC=CC=C1 LINCLFQLZHCRHE-UHFFFAOYSA-N 0.000 description 2
- 241000449794 Alabama argillacea Species 0.000 description 2
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N Ethylbenzene Chemical compound CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 2
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- SJFNDMHZXCUXSA-UHFFFAOYSA-M methoxymethyl(triphenyl)phosphanium;chloride Chemical compound [Cl-].C=1C=CC=CC=1[P+](C=1C=CC=CC=1)(COC)C1=CC=CC=C1 SJFNDMHZXCUXSA-UHFFFAOYSA-M 0.000 description 1
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- WRECIMRULFAWHA-UHFFFAOYSA-N trimethyl borate Chemical compound COB(OC)OC WRECIMRULFAWHA-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C07C17/16—Preparation of halogenated hydrocarbons by replacement by halogens of hydroxyl groups
-
- 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
- A01N29/00—Biocides, pest repellants or attractants, or plant growth regulators containing halogenated hydrocarbons
- A01N29/10—Halogen attached to an aliphatic side chain of an aromatic ring system
-
- 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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/08—Oxygen or sulfur directly attached to an aromatic ring system
- A01N31/14—Ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/26—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton
- C07C17/263—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions
- C07C17/2637—Preparation of halogenated hydrocarbons by reactions involving an increase in the number of carbon atoms in the skeleton by condensation reactions between a compound containing only oxygen and possibly halogen as hetero-atoms and a halogenated hydrocarbon
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/24—Halogenated aromatic hydrocarbons with unsaturated side chains
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C255/00—Carboxylic acid nitriles
- C07C255/01—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms
- C07C255/32—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring
- C07C255/35—Carboxylic acid nitriles having cyano groups bound to acyclic carbon atoms having cyano groups bound to acyclic carbon atoms of a carbon skeleton containing at least one six-membered aromatic ring the carbon skeleton being further substituted by halogen atoms, or by nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C33/00—Unsaturated compounds having hydroxy or O-metal groups bound to acyclic carbon atoms
- C07C33/40—Halogenated unsaturated alcohols
- C07C33/46—Halogenated unsaturated alcohols containing only six-membered aromatic rings as cyclic parts
- C07C33/48—Halogenated unsaturated alcohols containing only six-membered aromatic rings as cyclic parts with unsaturation outside the aromatic rings
- C07C33/483—Monocyclic
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/257—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings
- C07C43/29—Ethers having an ether-oxygen atom bound to carbon atoms both belonging to six-membered aromatic rings containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/27—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation
- C07C45/29—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups
- C07C45/298—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by oxidation of hydroxy groups with manganese derivatives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/44—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by reduction and hydrolysis of nitriles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
- C07C45/51—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition
- C07C45/511—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups
- C07C45/513—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds by pyrolysis, rearrangement or decomposition involving transformation of singly bound oxygen functional groups to >C = O groups the singly bound functional group being an etherified hydroxyl group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C47/00—Compounds having —CHO groups
- C07C47/20—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms
- C07C47/24—Unsaturated compounds having —CHO groups bound to acyclic carbon atoms containing halogen
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
- C07C69/62—Halogen-containing esters
- C07C69/65—Halogen-containing esters of unsaturated acids
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic Table
- C07F9/02—Phosphorus compounds
- C07F9/28—Phosphorus compounds with one or more P—C bonds
- C07F9/54—Quaternary phosphonium compounds
- C07F9/5456—Arylalkanephosphonium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2601/00—Systems containing only non-condensed rings
- C07C2601/02—Systems containing only non-condensed rings with a three-membered ring
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Biochemistry (AREA)
- Molecular Biology (AREA)
- Plant Pathology (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US66022196A | 1996-06-03 | 1996-06-03 | |
| US08/819,623 US5849958A (en) | 1997-03-17 | 1997-03-17 | 1,4,diaryl-2-fluoro-2-butene insecticidal and acaricidal agents |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BG101535A BG101535A (en) | 1998-09-30 |
| BG63255B1 true BG63255B1 (bg) | 2001-07-31 |
Family
ID=27098022
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| BG101535A BG63255B1 (bg) | 1996-06-03 | 1997-05-29 | 1,4-диарил-2-флуоро-2-бутенови инсектицидни и акарицидни средства |
Country Status (29)
| Country | Link |
|---|---|
| EP (1) | EP0811593B1 (OSRAM) |
| JP (1) | JPH1072385A (OSRAM) |
| KR (1) | KR100554014B1 (OSRAM) |
| CN (1) | CN1215030C (OSRAM) |
| AR (1) | AR007373A1 (OSRAM) |
| AT (1) | ATE221037T1 (OSRAM) |
| AU (1) | AU729500B2 (OSRAM) |
| BG (1) | BG63255B1 (OSRAM) |
| BR (1) | BR9703426A (OSRAM) |
| CA (1) | CA2206585A1 (OSRAM) |
| CO (1) | CO4771143A1 (OSRAM) |
| CZ (1) | CZ295292B6 (OSRAM) |
| DE (1) | DE69714145T2 (OSRAM) |
| DK (1) | DK0811593T3 (OSRAM) |
| ES (1) | ES2180895T3 (OSRAM) |
| GE (1) | GEP19991769B (OSRAM) |
| HU (1) | HUP9700983A3 (OSRAM) |
| ID (1) | ID17280A (OSRAM) |
| IL (1) | IL120966A (OSRAM) |
| IN (1) | IN182910B (OSRAM) |
| MD (1) | MD1971B2 (OSRAM) |
| NO (1) | NO308408B1 (OSRAM) |
| NZ (1) | NZ314977A (OSRAM) |
| PL (1) | PL320373A1 (OSRAM) |
| PT (1) | PT811593E (OSRAM) |
| SG (1) | SG52982A1 (OSRAM) |
| SK (1) | SK284663B6 (OSRAM) |
| TR (1) | TR199700452A3 (OSRAM) |
| YU (1) | YU22897A (OSRAM) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW467889B (en) * | 1997-11-12 | 2001-12-11 | American Cyanamid Co | 1,4-diaryl-2,3-difluoro-2-butene insecticidal and acaricidal agents |
| US6235754B1 (en) * | 1998-01-30 | 2001-05-22 | American Cyanamid Company | Methods and compositions for protecting animals and humans against attack and infestation by arthropod and helminth parasites |
| IL127852A0 (en) * | 1998-01-30 | 1999-10-28 | American Cyanamid Co | Methods and compositions for protecting animals and humans against attack and infestation by arthropod and helminth parasites |
| BR9915368A (pt) * | 1998-11-16 | 2001-08-14 | Basf Ag | Composto, e, processo para a preparação de um cosposto |
| US6646166B1 (en) | 1998-11-16 | 2003-11-11 | Basf Aktiengesellschaft | Processes for the preparation of 1,4-diaryl-2-fluoro-1,3-butadiene and 1,4-diaryl-2-fluoro 2 butene compounds |
| US6291721B1 (en) * | 1999-08-12 | 2001-09-18 | American Cyanamid Co. | Processes for the preparation of 2-arylvinyl alkyl ether and 1,4-diaryl-2-fluoro-2-butene compounds |
| US6342642B1 (en) | 1999-11-09 | 2002-01-29 | Basf Aktiengesellschaft | 1,4-diaryl-2-fluoro-1-buten-3-ol compounds and their use in the preparation of 1,4-diaryl-2-fluoro-1,3-butadiene and 1,4-diaryl-2-fluoro-2-butene compounds |
| DE60109914T2 (de) * | 2000-05-04 | 2006-02-09 | Basf Ag | 1,4-diaryl-2-fluoro-4-cyano-2-buten-derivate, verfahren zu ihrer herstellung und zwischenprodukte für dieses verfahren |
| JO3598B1 (ar) | 2006-10-10 | 2020-07-05 | Infinity Discovery Inc | الاحماض والاسترات البورونية كمثبطات اميد هيدروليز الحامض الدهني |
| AU2009233711B2 (en) | 2008-04-09 | 2015-02-12 | Infinity Pharmaceuticals, Inc | Inhibitors of fatty acid amide hydrolase |
| EP2531511A1 (en) | 2010-02-03 | 2012-12-12 | Infinity Pharmaceuticals, Inc. | Fatty acid amide hydrolase inhibitors |
Family Cites Families (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5248834A (en) * | 1984-04-09 | 1993-09-28 | British Technology Group Limited | Pesticides |
| US4975451A (en) * | 1989-03-02 | 1990-12-04 | Fmc Corporation | Insecticidal cyclopropyl di(aryl) 2-butenes |
| GB9219612D0 (en) * | 1992-09-16 | 1992-10-28 | Khambay Bhupinder P S | Pesticidal fluoroolefins |
| GB9408605D0 (en) * | 1994-04-29 | 1994-06-22 | British Tech Group | Pesticidal fluoroolefins |
-
1997
- 1997-05-29 AT AT97303657T patent/ATE221037T1/de not_active IP Right Cessation
- 1997-05-29 BG BG101535A patent/BG63255B1/bg unknown
- 1997-05-29 DE DE69714145T patent/DE69714145T2/de not_active Expired - Lifetime
- 1997-05-29 CO CO97029832A patent/CO4771143A1/es unknown
- 1997-05-29 JP JP9154272A patent/JPH1072385A/ja not_active Withdrawn
- 1997-05-29 CN CNB97105522XA patent/CN1215030C/zh not_active Expired - Fee Related
- 1997-05-29 EP EP97303657A patent/EP0811593B1/en not_active Expired - Lifetime
- 1997-05-29 ES ES97303657T patent/ES2180895T3/es not_active Expired - Lifetime
- 1997-05-29 PT PT97303657T patent/PT811593E/pt unknown
- 1997-05-29 DK DK97303657T patent/DK0811593T3/da active
- 1997-05-30 NZ NZ314977A patent/NZ314977A/xx unknown
- 1997-05-30 GE GEAP19973771A patent/GEP19991769B/en unknown
- 1997-05-30 CA CA002206585A patent/CA2206585A1/en not_active Abandoned
- 1997-05-31 KR KR1019970022346A patent/KR100554014B1/ko not_active Expired - Fee Related
- 1997-06-01 IL IL12096697A patent/IL120966A/xx not_active IP Right Cessation
- 1997-06-02 ID IDP971866A patent/ID17280A/id unknown
- 1997-06-02 TR TR97/00452A patent/TR199700452A3/tr unknown
- 1997-06-02 YU YU22897A patent/YU22897A/sh unknown
- 1997-06-02 SG SG1997001867A patent/SG52982A1/en unknown
- 1997-06-02 HU HU9700983A patent/HUP9700983A3/hu unknown
- 1997-06-02 MD MD97-0197A patent/MD1971B2/ro unknown
- 1997-06-02 AR ARP970102381A patent/AR007373A1/es active IP Right Grant
- 1997-06-02 NO NO972502A patent/NO308408B1/no not_active IP Right Cessation
- 1997-06-02 CZ CZ19971689A patent/CZ295292B6/cs not_active IP Right Cessation
- 1997-06-02 BR BR9703426A patent/BR9703426A/pt not_active Application Discontinuation
- 1997-06-02 AU AU24640/97A patent/AU729500B2/en not_active Ceased
- 1997-06-02 IN IN1030CA1997 patent/IN182910B/en unknown
- 1997-06-03 SK SK698-97A patent/SK284663B6/sk unknown
- 1997-06-03 PL PL97320373A patent/PL320373A1/xx unknown
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