AR095111A1 - Composición y método para controlar plagas - Google Patents
Composición y método para controlar plagasInfo
- Publication number
- AR095111A1 AR095111A1 ARP140100330A ARP140100330A AR095111A1 AR 095111 A1 AR095111 A1 AR 095111A1 AR P140100330 A ARP140100330 A AR P140100330A AR P140100330 A ARP140100330 A AR P140100330A AR 095111 A1 AR095111 A1 AR 095111A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- substituted
- atom
- hydrogen atom
- atoms
- Prior art date
Links
- 125000005843 halogen group Chemical group 0.000 abstract 24
- 150000001875 compounds Chemical class 0.000 abstract 15
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 13
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 8
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 6
- 150000001204 N-oxides Chemical class 0.000 abstract 6
- 241000607479 Yersinia pestis Species 0.000 abstract 6
- 125000004429 atom Chemical group 0.000 abstract 6
- -1 diphenoconazole Chemical compound 0.000 abstract 6
- 241000196324 Embryophyta Species 0.000 abstract 4
- 125000001188 haloalkyl group Chemical group 0.000 abstract 4
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 241000209094 Oryza Species 0.000 abstract 2
- 235000007164 Oryza sativa Nutrition 0.000 abstract 2
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000005010 perfluoroalkyl group Chemical group 0.000 abstract 2
- 235000009566 rice Nutrition 0.000 abstract 2
- ZMYFCFLJBGAQRS-IRXDYDNUSA-N (2R,3S)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@@]1(CN2N=CN=C2)[C@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IRXDYDNUSA-N 0.000 abstract 1
- LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 abstract 1
- PPDBOQMNKNNODG-NTEUORMPSA-N (5E)-5-(4-chlorobenzylidene)-2,2-dimethyl-1-(1,2,4-triazol-1-ylmethyl)cyclopentanol Chemical compound C1=NC=NN1CC1(O)C(C)(C)CC\C1=C/C1=CC=C(Cl)C=C1 PPDBOQMNKNNODG-NTEUORMPSA-N 0.000 abstract 1
- CIEXPHRYOLIQQD-CYBMUJFWSA-N (R)-furalaxyl Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-CYBMUJFWSA-N 0.000 abstract 1
- CKPCAYZTYMHQEX-NBVRZTHBSA-N (e)-1-(2,4-dichlorophenyl)-n-methoxy-2-pyridin-3-ylethanimine Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=N/OC)/CC1=CC=CN=C1 CKPCAYZTYMHQEX-NBVRZTHBSA-N 0.000 abstract 1
- JWUCHKBSVLQQCO-UHFFFAOYSA-N 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol Chemical compound C=1C=C(F)C=CC=1C(C=1C(=CC=CC=1)F)(O)CN1C=NC=N1 JWUCHKBSVLQQCO-UHFFFAOYSA-N 0.000 abstract 1
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 abstract 1
- VGPIBGGRCVEHQZ-UHFFFAOYSA-N 1-(biphenyl-4-yloxy)-3,3-dimethyl-1-(1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC(C=C1)=CC=C1C1=CC=CC=C1 VGPIBGGRCVEHQZ-UHFFFAOYSA-N 0.000 abstract 1
- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 abstract 1
- WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 abstract 1
- PZBPKYOVPCNPJY-UHFFFAOYSA-N 1-[2-(allyloxy)-2-(2,4-dichlorophenyl)ethyl]imidazole Chemical compound ClC1=CC(Cl)=CC=C1C(OCC=C)CN1C=NC=C1 PZBPKYOVPCNPJY-UHFFFAOYSA-N 0.000 abstract 1
- STMIIPIFODONDC-UHFFFAOYSA-N 2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)hexan-2-ol Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(O)(CCCC)CN1C=NC=N1 STMIIPIFODONDC-UHFFFAOYSA-N 0.000 abstract 1
- YABFPHSQTSFWQB-UHFFFAOYSA-N 2-(4-fluorophenyl)-1-(1,2,4-triazol-1-yl)-3-(trimethylsilyl)propan-2-ol Chemical compound C=1C=C(F)C=CC=1C(O)(C[Si](C)(C)C)CN1C=NC=N1 YABFPHSQTSFWQB-UHFFFAOYSA-N 0.000 abstract 1
- ZDRBJJNXJOSCLR-YZKQBBCCSA-N 2-amino-2-[(2r,3s,5s,6r)-5-amino-2-methyl-6-[(2r,3s,5s,6s)-2,3,4,5,6-pentahydroxycyclohexyl]oxyoxan-3-yl]iminoacetic acid;hydron;chloride Chemical compound Cl.N[C@H]1C[C@H](N=C(N)C(O)=O)[C@@H](C)O[C@@H]1OC1[C@H](O)[C@@H](O)C(O)[C@H](O)[C@@H]1O ZDRBJJNXJOSCLR-YZKQBBCCSA-N 0.000 abstract 1
- OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 abstract 1
- RQDJADAKIFFEKQ-UHFFFAOYSA-N 4-(4-chlorophenyl)-2-phenyl-2-(1,2,4-triazol-1-ylmethyl)butanenitrile Chemical compound C1=CC(Cl)=CC=C1CCC(C=1C=CC=CC=1)(C#N)CN1N=CN=C1 RQDJADAKIFFEKQ-UHFFFAOYSA-N 0.000 abstract 1
- PCCSBWNGDMYFCW-UHFFFAOYSA-N 5-methyl-5-(4-phenoxyphenyl)-3-(phenylamino)-1,3-oxazolidine-2,4-dione Chemical compound O=C1C(C)(C=2C=CC(OC=3C=CC=CC=3)=CC=2)OC(=O)N1NC1=CC=CC=C1 PCCSBWNGDMYFCW-UHFFFAOYSA-N 0.000 abstract 1
- 239000005730 Azoxystrobin Substances 0.000 abstract 1
- 239000005734 Benalaxyl Substances 0.000 abstract 1
- 239000005735 Benalaxyl-M Substances 0.000 abstract 1
- 239000005741 Bromuconazole Substances 0.000 abstract 1
- 239000005745 Captan Substances 0.000 abstract 1
- 239000005746 Carboxin Substances 0.000 abstract 1
- 239000005762 Dimoxystrobin Substances 0.000 abstract 1
- 239000005767 Epoxiconazole Substances 0.000 abstract 1
- 239000005772 Famoxadone Substances 0.000 abstract 1
- 239000005774 Fenamidone Substances 0.000 abstract 1
- 239000005775 Fenbuconazole Substances 0.000 abstract 1
- 239000005784 Fluoxastrobin Substances 0.000 abstract 1
- 239000005785 Fluquinconazole Substances 0.000 abstract 1
- 239000005787 Flutriafol Substances 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005795 Imazalil Substances 0.000 abstract 1
- 239000005796 Ipconazole Substances 0.000 abstract 1
- 239000005800 Kresoxim-methyl Substances 0.000 abstract 1
- 239000005807 Metalaxyl Substances 0.000 abstract 1
- 239000005808 Metalaxyl-M Substances 0.000 abstract 1
- 239000005868 Metconazole Substances 0.000 abstract 1
- XQJQCBDIXRIYRP-UHFFFAOYSA-N N-{2-[1,1'-bi(cyclopropyl)-2-yl]phenyl}-3-(difluoromethyl)-1-methyl-1pyrazole-4-carboxamide Chemical compound FC(F)C1=NN(C)C=C1C(=O)NC1=CC=CC=C1C1C(C2CC2)C1 XQJQCBDIXRIYRP-UHFFFAOYSA-N 0.000 abstract 1
- 239000005813 Penconazole Substances 0.000 abstract 1
- 239000005818 Picoxystrobin Substances 0.000 abstract 1
- 239000005820 Prochloraz Substances 0.000 abstract 1
- 239000005822 Propiconazole Substances 0.000 abstract 1
- 239000005869 Pyraclostrobin Substances 0.000 abstract 1
- 239000005834 Sedaxane Substances 0.000 abstract 1
- 239000005839 Tebuconazole Substances 0.000 abstract 1
- 239000005840 Tetraconazole Substances 0.000 abstract 1
- 239000005845 Tolclofos-methyl Substances 0.000 abstract 1
- 239000005846 Triadimenol Substances 0.000 abstract 1
- 239000005857 Trifloxystrobin Substances 0.000 abstract 1
- 239000005859 Triticonazole Substances 0.000 abstract 1
- 229930195482 Validamycin Natural products 0.000 abstract 1
- AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 abstract 1
- 229950000294 azaconazole Drugs 0.000 abstract 1
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 abstract 1
- CJPQIRJHIZUAQP-MRXNPFEDSA-N benalaxyl-M Chemical compound CC=1C=CC=C(C)C=1N([C@H](C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-MRXNPFEDSA-N 0.000 abstract 1
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 abstract 1
- 229940117949 captan Drugs 0.000 abstract 1
- GYSSRZJIHXQEHQ-UHFFFAOYSA-N carboxin Chemical compound S1CCOC(C)=C1C(=O)NC1=CC=CC=C1 GYSSRZJIHXQEHQ-UHFFFAOYSA-N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- WXUZAHCNPWONDH-DYTRJAOYSA-N dimoxystrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1COC1=CC(C)=CC=C1C WXUZAHCNPWONDH-DYTRJAOYSA-N 0.000 abstract 1
- 229960002125 enilconazole Drugs 0.000 abstract 1
- LMVPQMGRYSRMIW-KRWDZBQOSA-N fenamidone Chemical compound O=C([C@@](C)(N=C1SC)C=2C=CC=CC=2)N1NC1=CC=CC=C1 LMVPQMGRYSRMIW-KRWDZBQOSA-N 0.000 abstract 1
- GOWLARCWZRESHU-AQTBWJFISA-N ferimzone Chemical compound C=1C=CC=C(C)C=1C(/C)=N\NC1=NC(C)=CC(C)=N1 GOWLARCWZRESHU-AQTBWJFISA-N 0.000 abstract 1
- UFEODZBUAFNAEU-NLRVBDNBSA-N fluoxastrobin Chemical compound C=1C=CC=C(OC=2C(=C(OC=3C(=CC=CC=3)Cl)N=CN=2)F)C=1C(=N/OC)\C1=NOCCO1 UFEODZBUAFNAEU-NLRVBDNBSA-N 0.000 abstract 1
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 abstract 1
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 abstract 1
- 230000000855 fungicidal effect Effects 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- AGKSTYPVMZODRV-UHFFFAOYSA-N imibenconazole Chemical compound C1=CC(Cl)=CC=C1CSC(CN1N=CN=C1)=NC1=CC=C(Cl)C=C1Cl AGKSTYPVMZODRV-UHFFFAOYSA-N 0.000 abstract 1
- QTYCMDBMOLSEAM-UHFFFAOYSA-N ipconazole Chemical compound C1=NC=NN1CC1(O)C(C(C)C)CCC1CC1=CC=C(Cl)C=C1 QTYCMDBMOLSEAM-UHFFFAOYSA-N 0.000 abstract 1
- ZOTBXTZVPHCKPN-HTXNQAPBSA-N kresoxim-methyl Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC=C1C ZOTBXTZVPHCKPN-HTXNQAPBSA-N 0.000 abstract 1
- ZQEIXNIJLIKNTD-GFCCVEGCSA-N metalaxyl-M Chemical compound COCC(=O)N([C@H](C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-GFCCVEGCSA-N 0.000 abstract 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 abstract 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 abstract 1
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 abstract 1
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 abstract 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 abstract 1
- 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 abstract 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 abstract 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 abstract 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 abstract 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 abstract 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 abstract 1
- 239000002689 soil Substances 0.000 abstract 1
- 229910052717 sulfur Inorganic materials 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 abstract 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 abstract 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 abstract 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 abstract 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 abstract 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-IMTORBKUSA-N 0.000 abstract 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
-
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
-
- 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
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Abstract
Reivindicación 1: Una composición para controlar las plagas que comprende un compuesto seleccionado por la fórmula (1) o N-óxido de este y uno o más compuestos seleccionados del Grupo (A); la fórmula (1): caracterizada porque A¹ representa -NR⁷-, un átomo de oxígeno, o un átomo de azufre; A² representa un átomo de nitrógeno o =CR⁸-; R¹ representa un grupo alquilo C₁₋₆ que se puede sustituir con uno o más átomos o grupos seleccionados del Grupo X; R², R³ y R⁴ son iguales o diferentes entre sí y cada uno representa de modo independiente un grupo alquilo C₁₋₆ que se puede sustituir con uno o más átomos o grupos seleccionados del Grupo X, un grupo -OR¹⁰, un grupo -C(OR¹⁰)₃, un grupo -S(O)ₘR¹⁰, un grupo -S(O)₂NR¹⁰R¹¹, un grupo -NR¹⁰R¹¹, un grupo -NR¹⁰CO₂R¹¹, un grupo -NR¹⁰C(O)R¹¹, un grupo -CO₂R¹⁰, un grupo -C(O)R¹⁰, un grupo -C(O)NR¹⁰R¹¹, un grupo -SF₅, un grupo ciano, un grupo nitro, un átomo de halógeno, o un átomo de hidrógeno; R⁵ y R⁶ son iguales o diferentes entre sí y cada uno representa de modo independiente un grupo alquilo C₁₋₆ que se puede sustituir con uno o más átomos o grupos seleccionados del Grupo X, un grupo -OR¹⁰, un grupo -S(O)ₘR¹⁰, un grupo -S(O)₂NR¹⁰R¹¹, un grupo -NR¹⁰R¹¹, un grupo -NR¹⁰CO₂R¹¹, un grupo -NR¹⁰C(O)R¹¹, un grupo -CO₂R¹⁰, un grupo -C(O)R¹⁰, un grupo -C(O)NR¹⁰R¹¹, -OC(O)R¹⁰, un grupo -SF₅, un grupo -SH, un grupo ciano, un grupo nitro, un átomo de halógeno, o un átomo de hidrógeno, excepto por un caso en que R⁵ y R⁶ son átomos de hidrógeno; R⁷ representa un grupo alquilo C₁₋₆ que se puede sustituir con uno o más átomos o grupos seleccionados del Grupo W, un grupo -CO₂R¹⁰, un grupo -C(O)R¹⁰, un grupo -CHCO₂R¹⁰, un grupo cicloalquilo C₃₋₆, o un átomo de hidrógeno; R⁸ representa un grupo alquilo C₁₋₆ que se puede sustituir con uno o más átomos de halógeno, un grupo -OR¹⁰, un grupo -S(O)ₘR¹⁰, un grupo -NR¹⁰R¹¹, un grupo -CO₂R¹⁰, un grupo -C(O)R¹⁰, un grupo ciano, un grupo nitro, un átomo de halógeno, o un átomo de hidrógeno; R¹⁰ y R¹¹ son iguales o diferentes entre sí y cada uno representa de modo independiente un grupo alquilo C₁₋₆ que se puede sustituir con uno o más átomos o grupos seleccionados del Grupo X o un átomo de hidrógeno, excepto por un grupo -S(O)ₘR¹⁰ donde m es 1 ó 2 y R¹⁰ es un átomo de hidrógeno; m representa de modo independiente 0, 1 ó 2; y n representa 0, 1 ó 2; Grupo X que comprende: un grupo alcoxi C₁₋₆ que se puede sustituir con uno o más átomos de halógeno, un grupo cicloalquilo C₃₋₆ que se puede sustituir con uno o más átomos de halógeno o uno o más grupos alquilo C₁₋₃, un grupo ciano, un grupo hidroxi, y un átomo de halógeno; Grupo W que comprende: un grupo alcoxi C₁₋₆ que se puede sustituir con uno o más átomos de halógeno, un grupo cicloalquilo C₃₋₆ que se puede sustituir con uno o más átomos de halógeno, un grupo hidroxi, un átomo de halógeno, y un grupo ciano; Grupo (A): el grupo consiste en los subgrupos A-1, A-2, A-3, A-4, A-5, A-6, y A-7; subgrupo A-1: compuesto tipo azol seleccionado de tebuconazol, metconazol, difenoconazol, triticonazol, imazalilo, triadimenol, fluquinconazol, prochloraz, protioconazol, diniconazol, diniconazol M, ciproconazol, tetraconazol, ipconazol, triforine, pirifenox, fenarimol, nuarimol, oxpoconazolfumarato, pefurazoato, triflumizol, azaconazol, bitertanol, bromuconazol, epoxiconazol, fenbuconazol, flusilazol, flutriafol, hexaconazol, imibenconazol, miclobutanilo, penconazol, propiconazol, simeconazol, y triadimefon; subgrupo A-2: compuesto tipo estrobilurina seleccionado de kresoxim-metilo, azoxistrobina, piraclostrobina, picoxistrobina, enestrobina, trifloxistrobina, dimoxistrobina, fluoxastrobina, orisastrobina, famoxadona, fenamidona,metominostrobina, y un compuesto seleccionado por la fórmula (2); subgrupo A-3: compuesto tipo fenilamido seleccionado de metalaxilo, metalaxilo-M, furalaxil-M, benalaxilo, benalaxil-M, ofurace, y oxadixilo; subgrupo A-4: un compuesto para controlar el añublo del arroz seleccionado de probenazol, tiadinilo, triciclazol, piroquilon, clorhidrato de kasugamicina, ferimzona, isotianilo, ftalida, y tebufloquina; subgrupo A-5: un compuesto para controlar el añuble de la vaina del arroz seleccionado de pencicurona, furametpir, y validamicina; subgrupo A-6: compuesto tipo carboxamida seleccionado de carboxina, flutolanilo, Pentiopirad, fluopiram, penflufeno, sedaxano, y fluxapiroxad; subgrupo A-7: compuesto fungicida seleccionado de fludioxonilo, etaboxam, tolclofos-metilo, y captan. Reivindicación 8: La composición para controlar plagas de acuerdo con la reivindicación 1, caracterizada porque en el compuesto representado por la fórmula (1) o N-óxido de este es un compuesto seleccionado por la fórmula (3) o N-óxido de este; la fórmula (3): donde R¹ᵃ representa un grupo alquilo C₁₋₃; A²ᵃ representa un átomo de nitrógeno o =CR⁸ᵃ-; R³ᵃ representa un grupo alquilo C₁₋₃ que se puede sustituir con uno o más átomos de halógeno, un grupo -C(OR¹⁰ᵃ)₃, un átomo de halógeno, o un átomo de hidrógeno; R⁵ᵃ representa un grupo haloalquilo, un grupo -OR²⁰ᵃ, un grupo -S(O)ₘR²⁰ᵃ, o un átomo de halógeno; R⁶ᵃ representa un grupo ciano, un grupo -NR¹⁰ᵃR¹¹ᵃ, un átomo de halógeno, o un átomo de hidrógeno; R⁷ᵃ representa un grupo alquilo C₁₋₆ que se puede sustituir con uno o más átomos de halógeno; R⁸ᵃ representa un grupo -S(O)ₘR¹⁰ᵃ, un grupo ciano, un átomo de halógeno, o un átomo de hidrógeno; R¹⁰ᵃ y R¹¹ᵃ son iguales o diferentes entre sí y cada uno representa de modo independiente un grupo alquilo C₁₋₃ que se puede sustituir con uno o más átomos de halógeno; R²⁰ᵃ representa un grupo haloalquilo; m representa de modo independiente 0, 1 ó 2; y n representa 0, 1 ó 2. Reivindicación 9: La composición para controlar plagas de acuerdo con la reivindicación 1, caracterizada porque en el compuesto representado por la fórmula (1) o N-óxido de este es un compuesto seleccionado por la fórmula (4) o N-óxido de este; la fórmula (4): donde A²ᵇ representa un átomo de nitrógeno o =CR⁸ᵇ-; R³ᵇ representa un grupo alquilo C₁₋₃ que se puede sustituir con uno o más átomos de halógeno, un grupo -C(OR¹⁰ᵇ)₃, un átomo de halógeno, o un átomo de hidrógeno; R⁵ᵇ representa un grupo haloalquilo, un grupo -OR²⁰ᵇ, un grupo -S(O)ₘR²⁰ᵇ, o un átomo de halógeno; R⁸ᵇ representa un grupo -S(O)ₘR¹⁰ᵇ, un grupo ciano, un átomo de halógeno, o un átomo de hidrógeno; R¹⁰ᵇ representa de modo independiente un grupo alquilo C₁₋₃ que se puede sustituir con uno o más átomos de halógeno; R²⁰ᵇ representa un grupo haloalquilo; m representa de modo independiente 0, 1 ó 2; y n representa 0, 1 ó 2. Reivindicación 10: La composición para controlar plagas de acuerdo con la reivindicación 9, caracterizada porque en el compuesto representado por la fórmula (4) o N-óxido de este, R³ᵇ es un átomo de halógeno o un átomo de hidrógeno; R⁵ᵇ es un grupo perfluoroalquilo C₁₋₃, un grupo -OR³⁰ᵇ, o un grupo -S(O)ₘR³⁰ᵇ; R³⁰ᵇ es un grupo perfluoroalquilo C₁₋₃; y R⁸ᵇ es un átomo de halógeno o un átomo de hidrógeno. Reivindicación 21: Un método para controlar plagas, caracterizado porque comprende la etapa de aplicar una cantidad efectiva de la composición para controlar plagas de acuerdo con cualquiera de los Puntos 1 a 20 a plantas, semillas de plantas, bulbos, o un suelo donde crecen las plantas.
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| JP6350528B2 (ja) * | 2013-07-01 | 2018-07-04 | 住友化学株式会社 | 縮合複素環化合物及びその有害生物防除用途 |
| JP2014208695A (ja) * | 2014-07-04 | 2014-11-06 | 住友化学株式会社 | 有害生物防除組成物およびその用途 |
| US10005775B2 (en) | 2014-08-12 | 2018-06-26 | Syngenta Participations, Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| WO2016030229A1 (en) * | 2014-08-25 | 2016-03-03 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing substituents |
| JP6704397B2 (ja) | 2014-12-31 | 2020-06-03 | シンジェンタ パーティシペーションズ アーゲー | 硫黄含有置換基を有する殺有害生物的に活性な多環式誘導体 |
| JP6705458B2 (ja) * | 2015-09-08 | 2020-06-03 | 住友化学株式会社 | トリアゾール化合物の製造方法 |
| US10730872B2 (en) * | 2015-11-16 | 2020-08-04 | Syngenta Participations Ag | Pesticidally active heterocyclic derivatives with sulphur containing sustitutents |
| EP3436457B1 (en) | 2016-04-01 | 2022-07-20 | Basf Se | Bicyclic compounds |
| GB201617339D0 (en) | 2016-10-12 | 2016-11-23 | Lytix Biopharma As | Therapeutic compounds |
| BR112019013278B1 (pt) * | 2016-12-27 | 2022-10-04 | Nihon Nohyaku Co., Ltd | Composto heterocíclico condensado contendo um grupo oxima ou um sal do mesmo, composição inseticida compreendendo o mesmo ou seu sal, seu uso no tratamento de plantas ou solo, composição para controle de ectoparasitas compreendendo o mesmo ou seu sal, e seu uso no controle de ectoparasitas |
| EP4602918A3 (en) * | 2017-06-23 | 2025-10-15 | Basf Se | Pesticidal mixtures comprising a pyrazole compound |
| MA51609A (fr) | 2018-01-15 | 2021-04-21 | Syngenta Participations Ag | Dérivés hétérocycliques à activité pesticide comportant des substituants contenant du soufre |
| WO2021009311A1 (en) | 2019-07-17 | 2021-01-21 | Syngenta Crop Protection Ag | Pesticidally active heterocyclic derivatives with sulfur containing substituents |
| JP7581336B2 (ja) | 2019-09-20 | 2024-11-12 | シンジェンタ クロップ プロテクション アクチェンゲゼルシャフト | 硫黄及びスルホキシミン含有置換基を有する殺有害生物的に活性な複素環式誘導体 |
| CN112824402B (zh) * | 2019-11-21 | 2023-02-28 | 浙江省化工研究院有限公司 | 一类苯并咪唑类衍生物、其制备方法及应用 |
| CN112304921B (zh) * | 2020-10-23 | 2022-05-03 | 中国计量大学 | 一种基于拉曼光谱技术检测桑椹中花色素苷的方法 |
| WO2022200364A1 (en) | 2021-03-25 | 2022-09-29 | Syngenta Crop Protection Ag | Insect, acarina and nematode pest control |
| CN115181116B (zh) | 2022-07-29 | 2024-11-26 | 江苏中旗科技股份有限公司 | 具有含硫取代基的稠环化合物、制备方法、杀虫剂组合物及用途 |
| CN116849225B (zh) * | 2023-06-30 | 2025-07-01 | 陕西康禾立丰生物科技药业有限公司 | 一种含甲氧哌啶乙酯和oxazosulfyl的杀虫组合物及其应用 |
| WO2026020977A1 (zh) * | 2024-07-25 | 2026-01-29 | 青岛清原化合物有限公司 | 一种吡啶基取代的苯并杂环类化合物及其制备方法、杀虫组合物和应用 |
| CN119791120B (zh) * | 2025-01-09 | 2025-09-30 | 青岛滕润翔检测评价有限公司 | 一种杀虫组合物及其应用 |
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| WO1995027693A1 (en) | 1994-04-06 | 1995-10-19 | Shionogi & Co., Ltd. | α-SUBSTITUTED PHENYLACETIC ACID DERIVATIVE, PROCESS FOR PRODUCING THE SAME, AND AGRICULTURAL BACTERICIDE CONTAINING THE SAME |
| DE69618370T2 (de) * | 1995-04-11 | 2002-09-26 | Mitsui Chemicals, Inc. | Substituierte Thiophenderivate und diese als aktiver Bestandteil enthaltenden Fungizide für Land- und Gartenbauwirtschaft |
| DE19750012A1 (de) | 1997-11-12 | 1999-05-20 | Bayer Ag | Isothiazolcarbonsäureamide |
| NZ522775A (en) | 2000-05-30 | 2005-05-27 | Meiji Seika Kaisha | Rice blast control agents |
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| US6844295B2 (en) | 2000-07-04 | 2005-01-18 | Ube Industries, Ltd. | Benzoxazole compound, process for producing the same, and herbicide |
| DE10136065A1 (de) | 2001-07-25 | 2003-02-13 | Bayer Cropscience Ag | Pyrazolylcarboxanilide |
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| DE60303147T2 (de) * | 2002-08-12 | 2006-08-31 | Bayer Cropscience S.A. | Neues 2-pyridylethylbenzamid-derivat |
| DE102005007160A1 (de) | 2005-02-16 | 2006-08-24 | Basf Ag | Pyrazolcarbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| JP5369854B2 (ja) * | 2008-04-21 | 2013-12-18 | 住友化学株式会社 | 有害節足動物防除組成物および縮合複素環化合物 |
| US8273764B2 (en) | 2009-04-28 | 2012-09-25 | Sumitomo Chemical Company, Limited | Fused heterocyclic compounds and use thereof |
| JP5540640B2 (ja) | 2009-10-07 | 2014-07-02 | 住友化学株式会社 | 複素環化合物及びその有害節足動物防除用途 |
| CN103037694B (zh) | 2010-06-23 | 2014-08-13 | 住友化学株式会社 | 防治有害节肢动物的组合物和杂环化合物 |
| TW201242962A (en) * | 2010-12-01 | 2012-11-01 | Sumitomo Chemical Co | Pyrimidine compound and use for pest control thereof |
| WO2012086848A1 (en) * | 2010-12-24 | 2012-06-28 | Sumitomo Chemical Company, Limited | Fused heterocyclic compound and use for pest control thereof |
| TWI545119B (zh) * | 2011-08-04 | 2016-08-11 | 住友化學股份有限公司 | 稠合雜環化合物及其在病蟲害防制上之用途 |
| EP2857397B1 (en) * | 2012-05-30 | 2020-04-08 | Sumitomo Chemical Company Limited | Fused heterocyclic compound |
| US20150148308A1 (en) | 2012-06-15 | 2015-05-28 | Sumitomo Chemical Company, Limited | Pest control composition for harmful arthropods, and pest control method for harmful arthropods |
| WO2013187422A1 (ja) | 2012-06-15 | 2013-12-19 | 住友化学株式会社 | 有害節足動物防除組成物及び有害節足動物の防除方法 |
| WO2013187426A1 (ja) | 2012-06-15 | 2013-12-19 | 住友化学株式会社 | 有害節足動物の防除方法 |
| WO2013187424A1 (ja) | 2012-06-15 | 2013-12-19 | 住友化学株式会社 | 有害節足動物防除組成物及び有害節足動物の防除方法 |
| WO2013187425A1 (ja) | 2012-06-15 | 2013-12-19 | 住友化学株式会社 | 有害節足動物防除組成物及び有害節足動物の防除方法 |
| EP2865672A4 (en) * | 2012-06-22 | 2015-12-16 | Sumitomo Chemical Co | CONDENSED HETEROCYCLIC COMPOUND |
| EP2938601B1 (en) * | 2012-12-27 | 2018-05-16 | Sumitomo Chemical Company Limited | Fused oxazole compounds and use thereof for pest control |
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| BR112015018188A2 (pt) | 2017-07-18 |
| BR112015018188B1 (pt) | 2020-08-25 |
| TW201444817A (zh) | 2014-12-01 |
| EP2952097A1 (en) | 2015-12-09 |
| WO2014119672A1 (ja) | 2014-08-07 |
| CA2898638A1 (en) | 2014-08-07 |
| AU2014213387B2 (en) | 2017-08-03 |
| US9974307B2 (en) | 2018-05-22 |
| CN105163587B (zh) | 2018-01-12 |
| PH12015501634B1 (en) | 2019-09-25 |
| PH12015501634A1 (en) | 2015-10-12 |
| AU2014213387A1 (en) | 2015-08-06 |
| EP2952097B1 (en) | 2018-10-10 |
| JPWO2014119672A1 (ja) | 2017-01-26 |
| KR20150113094A (ko) | 2015-10-07 |
| US20150359222A1 (en) | 2015-12-17 |
| KR102106662B1 (ko) | 2020-05-04 |
| CN105163587A (zh) | 2015-12-16 |
| TWI614242B (zh) | 2018-02-11 |
| JP6178345B2 (ja) | 2017-08-09 |
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