AR065576A1 - Mezclas activas pesticidas que comprenden compuestos de aminotiazolina - Google Patents
Mezclas activas pesticidas que comprenden compuestos de aminotiazolinaInfo
- Publication number
- AR065576A1 AR065576A1 ARP080100876A ARP080100876A AR065576A1 AR 065576 A1 AR065576 A1 AR 065576A1 AR P080100876 A ARP080100876 A AR P080100876A AR P080100876 A ARP080100876 A AR P080100876A AR 065576 A1 AR065576 A1 AR 065576A1
- Authority
- AR
- Argentina
- Prior art keywords
- alpha
- class
- hydrogen
- methyl
- compounds
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 7
- 239000000203 mixture Substances 0.000 title abstract 6
- 239000000575 pesticide Substances 0.000 title abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 5
- 229910052739 hydrogen Inorganic materials 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- -1 alanicarb Chemical compound 0.000 abstract 4
- 125000001153 fluoro group Chemical group F* 0.000 abstract 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 4
- 125000001246 bromo group Chemical group Br* 0.000 abstract 3
- 125000001309 chloro group Chemical group Cl* 0.000 abstract 3
- 239000003112 inhibitor Substances 0.000 abstract 3
- GRVDJDISBSALJP-UHFFFAOYSA-N methyloxidanyl Chemical compound [O]C GRVDJDISBSALJP-UHFFFAOYSA-N 0.000 abstract 3
- KAATUXNTWXVJKI-NSHGMRRFSA-N (1R)-cis-(alphaS)-cypermethrin Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-NSHGMRRFSA-N 0.000 abstract 2
- 241000238631 Hexapoda Species 0.000 abstract 2
- 241000244206 Nematoda Species 0.000 abstract 2
- 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 abstract 2
- 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 abstract 2
- 239000000556 agonist Substances 0.000 abstract 2
- 230000015572 biosynthetic process Effects 0.000 abstract 2
- OEBRKCOSUFCWJD-UHFFFAOYSA-N dichlorvos Chemical compound COP(=O)(OC)OC=C(Cl)Cl OEBRKCOSUFCWJD-UHFFFAOYSA-N 0.000 abstract 2
- 150000007857 hydrazones Chemical class 0.000 abstract 2
- 150000008048 phenylpyrazoles Chemical class 0.000 abstract 2
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 abstract 2
- SNICXCGAKADSCV-JTQLQIEISA-N (-)-Nicotine Chemical compound CN1CCC[C@H]1C1=CC=CN=C1 SNICXCGAKADSCV-JTQLQIEISA-N 0.000 abstract 1
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 abstract 1
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 abstract 1
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 abstract 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 abstract 1
- NRPCZWUIOZTKHN-FMIVXFBMSA-N (ne)-n-[1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3,5-dimethyl-1,3,5-triazinan-2-ylidene]nitramide Chemical compound C1N(C)CN(C)\C(=N/[N+]([O-])=O)N1CC1=CN=C(Cl)S1 NRPCZWUIOZTKHN-FMIVXFBMSA-N 0.000 abstract 1
- RAIPHJJURHTUIC-UHFFFAOYSA-N 1,3-thiazol-2-amine Chemical compound NC1=NC=CS1 RAIPHJJURHTUIC-UHFFFAOYSA-N 0.000 abstract 1
- BOTNFCTYKJBUMU-UHFFFAOYSA-N 2-[4-(2-methylpropyl)piperazin-4-ium-1-yl]-2-oxoacetate Chemical compound CC(C)C[NH+]1CCN(C(=O)C([O-])=O)CC1 BOTNFCTYKJBUMU-UHFFFAOYSA-N 0.000 abstract 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 abstract 1
- ZOCSXAVNDGMNBV-UHFFFAOYSA-N 5-amino-1-[2,6-dichloro-4-(trifluoromethyl)phenyl]-4-[(trifluoromethyl)sulfinyl]-1H-pyrazole-3-carbonitrile Chemical compound NC1=C(S(=O)C(F)(F)F)C(C#N)=NN1C1=C(Cl)C=C(C(F)(F)F)C=C1Cl ZOCSXAVNDGMNBV-UHFFFAOYSA-N 0.000 abstract 1
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 abstract 1
- HBAQYPYDRFILMT-UHFFFAOYSA-N 8-[3-(1-cyclopropylpyrazol-4-yl)-1H-pyrazolo[4,3-d]pyrimidin-5-yl]-3-methyl-3,8-diazabicyclo[3.2.1]octan-2-one Chemical class C1(CC1)N1N=CC(=C1)C1=NNC2=C1N=C(N=C2)N1C2C(N(CC1CC2)C)=O HBAQYPYDRFILMT-UHFFFAOYSA-N 0.000 abstract 1
- 239000005660 Abamectin Substances 0.000 abstract 1
- 239000005875 Acetamiprid Substances 0.000 abstract 1
- 229940122578 Acetylcholine receptor agonist Drugs 0.000 abstract 1
- 229940100578 Acetylcholinesterase inhibitor Drugs 0.000 abstract 1
- 239000005877 Alpha-Cypermethrin Substances 0.000 abstract 1
- 241000239223 Arachnida Species 0.000 abstract 1
- 239000005878 Azadirachtin Substances 0.000 abstract 1
- 239000005653 Bifenazate Substances 0.000 abstract 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 1
- 239000005885 Buprofezin Substances 0.000 abstract 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 abstract 1
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 abstract 1
- 229920002101 Chitin Polymers 0.000 abstract 1
- 229940127437 Chloride Channel Antagonists Drugs 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- 239000005654 Clofentezine Substances 0.000 abstract 1
- 239000005946 Cypermethrin Substances 0.000 abstract 1
- 239000005892 Deltamethrin Substances 0.000 abstract 1
- 239000005947 Dimethoate Substances 0.000 abstract 1
- 239000005899 Fipronil Substances 0.000 abstract 1
- 239000005900 Flonicamid Substances 0.000 abstract 1
- 239000005906 Imidacloprid Substances 0.000 abstract 1
- 239000005914 Metaflumizone Substances 0.000 abstract 1
- MIFOMMKAVSCNKQ-HWIUFGAZSA-N Metaflumizone Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)N\N=C(C=1C=C(C=CC=1)C(F)(F)F)\CC1=CC=C(C#N)C=C1 MIFOMMKAVSCNKQ-HWIUFGAZSA-N 0.000 abstract 1
- 241001465754 Metazoa Species 0.000 abstract 1
- 239000005951 Methiocarb Substances 0.000 abstract 1
- 239000005916 Methomyl Substances 0.000 abstract 1
- 239000005918 Milbemectin Substances 0.000 abstract 1
- 239000005950 Oxamyl Substances 0.000 abstract 1
- 239000005926 Pyridalyl Substances 0.000 abstract 1
- ISRUGXGCCGIOQO-UHFFFAOYSA-N Rhoden Chemical compound CNC(=O)OC1=CC=CC=C1OC(C)C ISRUGXGCCGIOQO-UHFFFAOYSA-N 0.000 abstract 1
- 108010052164 Sodium Channels Proteins 0.000 abstract 1
- 102000018674 Sodium Channels Human genes 0.000 abstract 1
- 239000005930 Spinosad Substances 0.000 abstract 1
- 239000005664 Spirodiclofen Substances 0.000 abstract 1
- 239000005937 Tebufenozide Substances 0.000 abstract 1
- 239000005940 Thiacloprid Substances 0.000 abstract 1
- 239000005941 Thiamethoxam Substances 0.000 abstract 1
- KAATUXNTWXVJKI-QPIRBTGLSA-N [(s)-cyano-(3-phenoxyphenyl)methyl] 3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-QPIRBTGLSA-N 0.000 abstract 1
- 229950008167 abamectin Drugs 0.000 abstract 1
- YASYVMFAVPKPKE-UHFFFAOYSA-N acephate Chemical compound COP(=O)(SC)NC(C)=O YASYVMFAVPKPKE-UHFFFAOYSA-N 0.000 abstract 1
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 abstract 1
- 229960004373 acetylcholine Drugs 0.000 abstract 1
- QGLZXHRNAYXIBU-WEVVVXLNSA-N aldicarb Chemical compound CNC(=O)O\N=C\C(C)(C)SC QGLZXHRNAYXIBU-WEVVVXLNSA-N 0.000 abstract 1
- 229960002587 amitraz Drugs 0.000 abstract 1
- QXAITBQSYVNQDR-ZIOPAAQOSA-N amitraz Chemical compound C=1C=C(C)C=C(C)C=1/N=C/N(C)\C=N\C1=CC=C(C)C=C1C QXAITBQSYVNQDR-ZIOPAAQOSA-N 0.000 abstract 1
- 239000005557 antagonist Substances 0.000 abstract 1
- VEHPJKVTJQSSKL-UHFFFAOYSA-N azadirachtin Natural products O1C2(C)C(C3(C=COC3O3)O)CC3C21C1(C)C(O)C(OCC2(OC(C)=O)C(CC3OC(=O)C(C)=CC)OC(C)=O)C2C32COC(C(=O)OC)(O)C12 VEHPJKVTJQSSKL-UHFFFAOYSA-N 0.000 abstract 1
- FTNJWQUOZFUQQJ-IRYYUVNJSA-N azadirachtin A Natural products C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C/C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-IRYYUVNJSA-N 0.000 abstract 1
- FTNJWQUOZFUQQJ-NDAWSKJSSA-N azadirachtin A Chemical compound C([C@@H]([C@]1(C=CO[C@H]1O1)O)[C@]2(C)O3)[C@H]1[C@]23[C@]1(C)[C@H](O)[C@H](OC[C@@]2([C@@H](C[C@@H]3OC(=O)C(\C)=C\C)OC(C)=O)C(=O)OC)[C@@H]2[C@]32CO[C@@](C(=O)OC)(O)[C@@H]12 FTNJWQUOZFUQQJ-NDAWSKJSSA-N 0.000 abstract 1
- RQVGAIADHNPSME-UHFFFAOYSA-N azinphos-ethyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OCC)OCC)N=NC2=C1 RQVGAIADHNPSME-UHFFFAOYSA-N 0.000 abstract 1
- CJJOSEISRRTUQB-UHFFFAOYSA-N azinphos-methyl Chemical group C1=CC=C2C(=O)N(CSP(=S)(OC)OC)N=NC2=C1 CJJOSEISRRTUQB-UHFFFAOYSA-N 0.000 abstract 1
- FYZBOYWSHKHDMT-UHFFFAOYSA-N benfuracarb Chemical compound CCOC(=O)CCN(C(C)C)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 FYZBOYWSHKHDMT-UHFFFAOYSA-N 0.000 abstract 1
- RJNJWHFSKNJCTB-UHFFFAOYSA-N benzylurea Chemical class NC(=O)NCC1=CC=CC=C1 RJNJWHFSKNJCTB-UHFFFAOYSA-N 0.000 abstract 1
- VHLKTXFWDRXILV-UHFFFAOYSA-N bifenazate Chemical compound C1=C(NNC(=O)OC(C)C)C(OC)=CC=C1C1=CC=CC=C1 VHLKTXFWDRXILV-UHFFFAOYSA-N 0.000 abstract 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical class CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-UXHICEINSA-N 0.000 abstract 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 1
- 229910052794 bromium Inorganic materials 0.000 abstract 1
- PRLVTUNWOQKEAI-VKAVYKQESA-N buprofezin Chemical compound O=C1N(C(C)C)\C(=N\C(C)(C)C)SCN1C1=CC=CC=C1 PRLVTUNWOQKEAI-VKAVYKQESA-N 0.000 abstract 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 abstract 1
- 229960005286 carbaryl Drugs 0.000 abstract 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 abstract 1
- DUEPRVBVGDRKAG-UHFFFAOYSA-N carbofuran Chemical compound CNC(=O)OC1=CC=CC2=C1OC(C)(C)C2 DUEPRVBVGDRKAG-UHFFFAOYSA-N 0.000 abstract 1
- JLQUFIHWVLZVTJ-UHFFFAOYSA-N carbosulfan Chemical compound CCCCN(CCCC)SN(C)C(=O)OC1=CC=CC2=C1OC(C)(C)C2 JLQUFIHWVLZVTJ-UHFFFAOYSA-N 0.000 abstract 1
- 239000003467 chloride channel stimulating agent Substances 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- UXADOQPNKNTIHB-UHFFFAOYSA-N clofentezine Chemical compound ClC1=CC=CC=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 UXADOQPNKNTIHB-UHFFFAOYSA-N 0.000 abstract 1
- 229940125904 compound 1 Drugs 0.000 abstract 1
- 230000001276 controlling effect Effects 0.000 abstract 1
- KAATUXNTWXVJKI-UHFFFAOYSA-N cypermethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OC(C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 KAATUXNTWXVJKI-UHFFFAOYSA-N 0.000 abstract 1
- 229960005424 cypermethrin Drugs 0.000 abstract 1
- 229960002483 decamethrin Drugs 0.000 abstract 1
- OWZREIFADZCYQD-NSHGMRRFSA-N deltamethrin Chemical compound CC1(C)[C@@H](C=C(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 OWZREIFADZCYQD-NSHGMRRFSA-N 0.000 abstract 1
- 230000001419 dependent effect Effects 0.000 abstract 1
- FHIVAFMUCKRCQO-UHFFFAOYSA-N diazinon Chemical compound CCOP(=S)(OCC)OC1=CC(C)=NC(C(C)C)=N1 FHIVAFMUCKRCQO-UHFFFAOYSA-N 0.000 abstract 1
- 229950001327 dichlorvos Drugs 0.000 abstract 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 abstract 1
- YKBZOVFACRVRJN-UHFFFAOYSA-N dinotefuran Chemical compound [O-][N+](=O)\N=C(/NC)NCC1CCOC1 YKBZOVFACRVRJN-UHFFFAOYSA-N 0.000 abstract 1
- GCKZANITAMOIAR-XWVCPFKXSA-N dsstox_cid_14566 Chemical compound [O-]C(=O)C1=CC=CC=C1.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H]([NH2+]C)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 GCKZANITAMOIAR-XWVCPFKXSA-N 0.000 abstract 1
- 150000002058 ecdysones Chemical class 0.000 abstract 1
- RDYMFSUJUZBWLH-SVWSLYAFSA-N endosulfan Chemical compound C([C@@H]12)OS(=O)OC[C@@H]1[C@]1(Cl)C(Cl)=C(Cl)[C@@]2(Cl)C1(Cl)Cl RDYMFSUJUZBWLH-SVWSLYAFSA-N 0.000 abstract 1
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 abstract 1
- 229940013764 fipronil Drugs 0.000 abstract 1
- RLQJEEJISHYWON-UHFFFAOYSA-N flonicamid Chemical compound FC(F)(F)C1=CC=NC=C1C(=O)NCC#N RLQJEEJISHYWON-UHFFFAOYSA-N 0.000 abstract 1
- GJEREQYJIQASAW-UHFFFAOYSA-N flufenerim Chemical compound CC(F)C1=NC=NC(NCCC=2C=CC(OC(F)(F)F)=CC=2)=C1Cl GJEREQYJIQASAW-UHFFFAOYSA-N 0.000 abstract 1
- 230000004927 fusion Effects 0.000 abstract 1
- 229960003692 gamma aminobutyric acid Drugs 0.000 abstract 1
- BTCSSZJGUNDROE-UHFFFAOYSA-N gamma-aminobutyric acid Chemical compound NCCCC(O)=O BTCSSZJGUNDROE-UHFFFAOYSA-N 0.000 abstract 1
- FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 abstract 1
- 229930000073 hydroprene Natural products 0.000 abstract 1
- HICUREFSAIZXFQ-JOWPUVSESA-N i9z29i000j Chemical compound C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\[C@H](OC(=O)C(=N/OC)\C=1C=CC=CC=1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 HICUREFSAIZXFQ-JOWPUVSESA-N 0.000 abstract 1
- 229940056881 imidacloprid Drugs 0.000 abstract 1
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 abstract 1
- 229930014550 juvenile hormone Natural products 0.000 abstract 1
- 239000002949 juvenile hormone Substances 0.000 abstract 1
- 150000003633 juvenile hormone derivatives Chemical class 0.000 abstract 1
- 150000002632 lipids Chemical class 0.000 abstract 1
- 239000007788 liquid Substances 0.000 abstract 1
- PWPJGUXAGUPAHP-UHFFFAOYSA-N lufenuron Chemical compound C1=C(Cl)C(OC(F)(F)C(C(F)(F)F)F)=CC(Cl)=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F PWPJGUXAGUPAHP-UHFFFAOYSA-N 0.000 abstract 1
- YFBPRJGDJKVWAH-UHFFFAOYSA-N methiocarb Chemical compound CNC(=O)OC1=CC(C)=C(SC)C(C)=C1 YFBPRJGDJKVWAH-UHFFFAOYSA-N 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 abstract 1
- QCAWEPFNJXQPAN-UHFFFAOYSA-N methoxyfenozide Chemical compound COC1=CC=CC(C(=O)NN(C(=O)C=2C=C(C)C=C(C)C=2)C(C)(C)C)=C1C QCAWEPFNJXQPAN-UHFFFAOYSA-N 0.000 abstract 1
- KBHDSWIXRODKSZ-UHFFFAOYSA-N methyl 5-chloro-2-(trifluoromethylsulfonylamino)benzoate Chemical compound COC(=O)C1=CC(Cl)=CC=C1NS(=O)(=O)C(F)(F)F KBHDSWIXRODKSZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- ZLBGSRMUSVULIE-GSMJGMFJSA-N milbemycin A3 Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 ZLBGSRMUSVULIE-GSMJGMFJSA-N 0.000 abstract 1
- KRTSDMXIXPKRQR-AATRIKPKSA-N monocrotophos Chemical compound CNC(=O)\C=C(/C)OP(=O)(OC)OC KRTSDMXIXPKRQR-AATRIKPKSA-N 0.000 abstract 1
- 229960002715 nicotine Drugs 0.000 abstract 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 abstract 1
- 229940079888 nitenpyram Drugs 0.000 abstract 1
- 235000015097 nutrients Nutrition 0.000 abstract 1
- KZAUOCCYDRDERY-UHFFFAOYSA-N oxamyl Chemical compound CNC(=O)ON=C(SC)C(=O)N(C)C KZAUOCCYDRDERY-UHFFFAOYSA-N 0.000 abstract 1
- 230000010627 oxidative phosphorylation Effects 0.000 abstract 1
- 244000045947 parasite Species 0.000 abstract 1
- 230000000590 parasiticidal effect Effects 0.000 abstract 1
- 229960000490 permethrin Drugs 0.000 abstract 1
- RLLPVAHGXHCWKJ-UHFFFAOYSA-N permethrin Chemical compound CC1(C)C(C=C(Cl)Cl)C1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-UHFFFAOYSA-N 0.000 abstract 1
- 230000000361 pesticidal effect Effects 0.000 abstract 1
- BULVZWIRKLYCBC-UHFFFAOYSA-N phorate Chemical compound CCOP(=S)(OCC)SCSCC BULVZWIRKLYCBC-UHFFFAOYSA-N 0.000 abstract 1
- IOUNQDKNJZEDEP-UHFFFAOYSA-N phosalone Chemical compound C1=C(Cl)C=C2OC(=O)N(CSP(=S)(OCC)OCC)C2=C1 IOUNQDKNJZEDEP-UHFFFAOYSA-N 0.000 abstract 1
- LMNZTLDVJIUSHT-UHFFFAOYSA-N phosmet Chemical compound C1=CC=C2C(=O)N(CSP(=S)(OC)OC)C(=O)C2=C1 LMNZTLDVJIUSHT-UHFFFAOYSA-N 0.000 abstract 1
- RGCLLPNLLBQHPF-HJWRWDBZSA-N phosphamidon Chemical compound CCN(CC)C(=O)C(\Cl)=C(/C)OP(=O)(OC)OC RGCLLPNLLBQHPF-HJWRWDBZSA-N 0.000 abstract 1
- 229960005235 piperonyl butoxide Drugs 0.000 abstract 1
- QHOQHJPRIBSPCY-UHFFFAOYSA-N pirimiphos-methyl Chemical compound CCN(CC)C1=NC(C)=CC(OP(=S)(OC)OC)=N1 QHOQHJPRIBSPCY-UHFFFAOYSA-N 0.000 abstract 1
- ZYHMJXZULPZUED-UHFFFAOYSA-N propargite Chemical compound C1=CC(C(C)(C)C)=CC=C1OC1C(OS(=O)OCC#C)CCCC1 ZYHMJXZULPZUED-UHFFFAOYSA-N 0.000 abstract 1
- AEHJMNVBLRLZKK-UHFFFAOYSA-N pyridalyl Chemical group N1=CC(C(F)(F)F)=CC=C1OCCCOC1=C(Cl)C=C(OCC=C(Cl)Cl)C=C1Cl AEHJMNVBLRLZKK-UHFFFAOYSA-N 0.000 abstract 1
- 230000001105 regulatory effect Effects 0.000 abstract 1
- MSHXTAQSSIEBQS-UHFFFAOYSA-N s-[3-carbamoylsulfanyl-2-(dimethylamino)propyl] carbamothioate;hydron;chloride Chemical compound [Cl-].NC(=O)SCC([NH+](C)C)CSC(N)=O MSHXTAQSSIEBQS-UHFFFAOYSA-N 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000003195 sodium channel blocking agent Substances 0.000 abstract 1
- 239000002689 soil Substances 0.000 abstract 1
- 239000007787 solid Substances 0.000 abstract 1
- 229940014213 spinosad Drugs 0.000 abstract 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 abstract 1
- 238000003786 synthesis reaction Methods 0.000 abstract 1
- 239000005936 tau-Fluvalinate Substances 0.000 abstract 1
- INISTDXBRIBGOC-XMMISQBUSA-N tau-fluvalinate Chemical compound N([C@H](C(C)C)C(=O)OC(C#N)C=1C=C(OC=2C=CC=CC=2)C=CC=1)C1=CC=C(C(F)(F)F)C=C1Cl INISTDXBRIBGOC-XMMISQBUSA-N 0.000 abstract 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 abstract 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 abstract 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 abstract 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 abstract 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 abstract 1
- 239000005943 zeta-Cypermethrin Substances 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Veterinary Medicine (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Organic Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Thiazole And Isothizaole Compounds (AREA)
Abstract
Reivindicacion 1: Mezclas pesticidas caracterizadas porque comprenden como compuestos activos: 1) al menos un compuesto de aminotiazolina 1 de la formula 1 en donde R1 está seleccionado de hidrogeno, COCH3, COH2OCH3, COCH2CH3 o COCH2C(CH3)3; R2 estáseleccionado de fluoro, cloro, bromo, CF3, CH3 o CH3O, R3 está seleccionado de hidrogeno, fluoro, cloro, bromo, CF3 o CH3, o R2 y R3 forman junto con -OCF2O- u -O-CH2-O- un anillo heterocíclico fusionado de 5 miembros; R4 está seleccionado dehidrogeno, fluoro, cloro, bromo, CF3, CH3O o CH3; R5, R6 están seleccionados de hidrogeno, cloro, fluoro, bromo, CH3, CH3O o CF3, en donde al menos uno de R5 o R6 no es hidrogeno; o sus tautomeros, enantiomeros, diastereomeros o sales, y 2) al menosun compuesto activo (2) seleccionado del grupo A que consiste en: A.1 Inhibidores de la acetilcolina esterasa seleccionados de triazemato o de la clase de carbamatos que consisten en aldicarb, alanicarb, benfuracarb, carbarilo, carbofurano,carbosulfano, metiocarb, metomilo, oxamilo, primicarb, propoxur y tiodicarb, o de la clase de organofosfatos que consisten en acefato, azinfos-etilo, azinfos-metilo, clorfenvinfos, clorpirifos, clorpirifos-metilo, demeton-S-metilo, diazinona,diclorvos/DDVP, dicrotofos, dimetoato, disulfotona, etiona, fenitrotiona, fentiona, isoxationa, malationa, metamidafos, metidationa, mevinfos, monocrotofos, oximetoato, oxidemeton-metilo, parationa, paration-metilo, fentoato, forato, fosalona,fosmet, fosfamidona, pirimifos-metilo, quinalfos, terbufos, tetraclorvinfos, triazofos y triclorfona; A.2 Antagonistas del canal de cloruro regulado por GABA seleccionados de te ciclodieno organocloro endosulfano, N-etil-2,2-dimetilpropionamid-2-(2,6-dicloro-alfa.alfa.alfa-trifluoro-p-toIil)hidrazona, N-etil-2,2-dicloro-1-metilciclopropan-carboxamid-2-(2,6-dicloro-alfa.alfa.alfa-trifluoro-p-tolil)hidrazona o de la clase de fenilpirazoles que consisten en acetoprol, etiprol, fipronilo,pirafluprol, piriprol, vaniliprol y el compuesto de fenilpirazol de formula (2); A.3 Moduladores del canal de sodio seleccionados de la clase de piretroides que consisten en aletrina, bifentrina, ciflutrina, lambda-cihalotrina, cipermetrina, alfa-cipermetrina, beta-cipermetrina, zeta-cipermetrina, deltametrina, esfenvalerato, etofenprox, fenpropatrina, fenvalerato, flucitrinato, tau-fluvalinato, permetrina, silafluofeno y tralometrina; A.4 Agonistas/antagonistas del receptor de acetilcolinanicotínica seleccionados de nicotín, clorhidrato de cartap, tiociclam o de la clase de neonicotinoides que consisten en acetamiprid, clotianidina, dinotefurano, imidacloprid, nitenpiram, tiacloprid, tiametoxam y AKD-1022; o el agonista del receptorde acetilcolina nicotínico alostético espinosad; A.5 Activadores del canal de cloruro seleccionados de abamectina, benzoato de emamectina, lepimectina o milbemectina; A.6 Mímicos de la hormona juvenil seleccionados de hidropreno, quinopreno,fenoxicarb o piriproxifeno; A.7 Compuestos que afectan la fosforilacion oxidativa seleccionados de diafentiurona, oxido de fenbutatina, propargita o clorfenapir; A.8 Inhibidores de la biosíntesis de la quitina seleccionado de buprofezina o de laclase de bencilureas que consisten en bistriflurona, diflubenzurona, flufenoxurona, hexaflumurona, lufenurona, novalurona y teflubenzurona; A.9 Disruptores de fusion seleccionados de ciromazina o de la clase de agonistas de ecdisona que consisten enmetoxifenozida, tebufenozida y azadiractina; A.10 Inhibidores del transporte de electrones microcondriales seleccionados de piridabeno, tolfenpirad o flufenerim. A.11 Bloqueadores del canal de sodio dependiente de voltaje, seleccionados deindoxacarb o metaflumizona; A.12 Inhibidores de la síntesis de lípidos seleccionados de espirodiclofeno, espiromesifeno o espirotetramato; A.13 Grupo de diversos compuestos que consisten en amidoflumet, amitraz, bifenazato, clofentezina,cienopirafeno, ciflumetofeno, etoxazol, flonicamid, flubendiamina, flupirazofos, hexitiazox, butoxido de piperonilo, pimetrozina, piridalilo, pirifluquinazona, clorantraniliprol, el compuesto de antranilamida de formula (3) y los compuestos desulfoximina de formulas (4) en cantidades sinérgicamente efectivas. Reivindicacion 22: Un método de control de insectos, arácnidos o nematodos caracterizado porque comprende poner en contacto un insecto, ácaro o nematodo o su suministro de comida,hábitat, suelos nutrientes o su locus con una mezcla de acuerdo con cualquiera de las reivindicaciones 1 a 20 en cantidades de eficacia pesticida. Reivindicacion 30: El uso de una mezcla de acuerdo con cualquiera de las reivindicaciones 1 a 20,caracterizado porque es para combatir parásitos en y sobre animales. Reivindicacion 32: Una composicion pesticida o parasiticida, caracterizada porque comprende un portador líquido o solido y una mezcla de acuerdo con cualquiera de lasreivindicaciones 1 a 20.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US89236507P | 2007-03-01 | 2007-03-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR065576A1 true AR065576A1 (es) | 2009-06-17 |
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080100876A AR065576A1 (es) | 2007-03-01 | 2008-02-29 | Mezclas activas pesticidas que comprenden compuestos de aminotiazolina |
Country Status (20)
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| US (1) | US8153560B2 (es) |
| EP (1) | EP2063711A1 (es) |
| JP (1) | JP5511393B2 (es) |
| KR (1) | KR20090116821A (es) |
| CN (1) | CN101621928A (es) |
| AR (1) | AR065576A1 (es) |
| AU (1) | AU2008220893A1 (es) |
| BR (1) | BRPI0807371A2 (es) |
| CA (1) | CA2679254A1 (es) |
| CL (1) | CL2008000632A1 (es) |
| CR (1) | CR11045A (es) |
| EA (1) | EA200901143A1 (es) |
| EC (1) | ECSP099643A (es) |
| IL (1) | IL200229A0 (es) |
| MA (1) | MA31255B1 (es) |
| MX (1) | MX2009008403A (es) |
| PE (1) | PE20090627A1 (es) |
| TW (1) | TW200900005A (es) |
| UY (1) | UY30945A1 (es) |
| WO (1) | WO2008104503A1 (es) |
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| PT1380209E (pt) * | 2001-04-17 | 2012-09-27 | Nihon Nohyaku Co Ltd | Composição de agente de controlo de pragas e método de utilização da mesma |
| BRPI0809575B8 (pt) * | 2007-04-12 | 2019-08-20 | Basf Se | misturas pesticidas, métodos para proteger plantas contra o ataque ou infestação por insetos, acarídeos ou nematódeos, e para proteger semente, uso de uma mistura, e, composição pesticida ou parasiticida |
| CA2691573A1 (en) * | 2007-07-03 | 2009-01-08 | Basf Se | 1-(azolin-2-yl)amino-1,2-diphenylethane compounds for combating animal pests |
| JP5504159B2 (ja) * | 2007-07-30 | 2014-05-28 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | 外部寄生虫の防除方法 |
| BR122018004457B1 (pt) * | 2007-11-16 | 2019-04-16 | Basf Se | Mistura pesticida, composição pesticida, métodos para controlar fungos fitopatogênicos nocivos, para proteger plantas, e para a proteção de semente, e, uso de uma mistura |
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| DE10251513A1 (de) * | 2002-11-04 | 2004-05-19 | Basf Ag | Übergangsmetallkatalysatoren für (Co)Polymerisation von olefinischen Monomeren |
| WO2005063724A1 (en) * | 2003-12-23 | 2005-07-14 | Basf Aktiengesellschaft | 1-(azolin-2-yl) amino-1,2-diphenylethane compounds for combatting insects, arachnids and nematodes |
| MX2007014225A (es) | 2005-05-19 | 2008-02-07 | Bayer Cropscience Ag | Insecticidas de derivados de heteroarilo y heterociclicos de bencilamino sustituido. |
| ATE491692T1 (de) * | 2005-05-24 | 2011-01-15 | Basf Se | 1-(imidazolin-2-yl)amino-1,2-diphenylethan- verbindungen zur bekämpfung von tierpestkrankheiten |
| US7652023B2 (en) * | 2005-11-23 | 2010-01-26 | Bristol-Myers Squibb Company | Heterocyclic CETP inhibitors |
| UA91395C2 (ru) | 2005-12-22 | 2010-07-26 | Басф Сэ | 1-(азолин-2-ил)-амино-1-фенил-2-гетарилетановое соединение, инсектицидная композиция на ее основе и способы борьбы с насекомыми (варианты) |
| US7989394B2 (en) | 2006-06-30 | 2011-08-02 | Basf Se | Substituted 1-(azolin-2-yl)-amino-2-aryl-1-hetaryl-ethane compounds |
| CA2691573A1 (en) | 2007-07-03 | 2009-01-08 | Basf Se | 1-(azolin-2-yl)amino-1,2-diphenylethane compounds for combating animal pests |
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2008
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- 2008-02-22 JP JP2009551931A patent/JP5511393B2/ja not_active Expired - Fee Related
- 2008-02-22 MX MX2009008403A patent/MX2009008403A/es unknown
- 2008-02-22 EA EA200901143A patent/EA200901143A1/ru unknown
- 2008-02-22 BR BRPI0807371-6A patent/BRPI0807371A2/pt not_active IP Right Cessation
- 2008-02-22 EP EP08709179A patent/EP2063711A1/en not_active Withdrawn
- 2008-02-22 CN CN200880006811A patent/CN101621928A/zh active Pending
- 2008-02-22 AU AU2008220893A patent/AU2008220893A1/en not_active Abandoned
- 2008-02-22 CA CA002679254A patent/CA2679254A1/en not_active Abandoned
- 2008-02-22 WO PCT/EP2008/052158 patent/WO2008104503A1/en not_active Ceased
- 2008-02-22 KR KR1020097020530A patent/KR20090116821A/ko not_active Withdrawn
- 2008-02-29 CL CL200800632A patent/CL2008000632A1/es unknown
- 2008-02-29 TW TW097107208A patent/TW200900005A/zh unknown
- 2008-02-29 AR ARP080100876A patent/AR065576A1/es not_active Application Discontinuation
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- 2008-02-29 PE PE2008000421A patent/PE20090627A1/es not_active Application Discontinuation
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2009
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- 2009-09-15 MA MA32223A patent/MA31255B1/fr unknown
- 2009-09-22 EC EC2009009643A patent/ECSP099643A/es unknown
- 2009-09-29 CR CR11045A patent/CR11045A/es not_active Application Discontinuation
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| AU2008220893A1 (en) | 2008-09-04 |
| UY30945A1 (es) | 2008-09-02 |
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| BRPI0807371A2 (pt) | 2014-05-06 |
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| WO2008104503A1 (en) | 2008-09-04 |
| CR11045A (es) | 2009-10-23 |
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| EP2063711A1 (en) | 2009-06-03 |
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| PE20090627A1 (es) | 2009-06-20 |
| IL200229A0 (en) | 2010-04-29 |
| US8153560B2 (en) | 2012-04-10 |
| MA31255B1 (fr) | 2010-03-01 |
| EA200901143A1 (ru) | 2010-04-30 |
| ECSP099643A (es) | 2009-10-30 |
| JP2010520230A (ja) | 2010-06-10 |
| JP5511393B2 (ja) | 2014-06-04 |
| TW200900005A (en) | 2009-01-01 |
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