JP2016526539A5 - - Google Patents

Info

Publication number

JP2016526539A5

JP2016526539A5 JP2016520409A JP2016520409A JP2016526539A5 JP 2016526539 A5 JP2016526539 A5 JP 2016526539A5 JP 2016520409 A JP2016520409 A JP 2016520409A JP 2016520409 A JP2016520409 A JP 2016520409A JP 2016526539 A5 JP2016526539 A5 JP 2016526539A5

Authority

JP

Japan

Prior art keywords

alkyl

halo

cyano

alkoxy

methyl

Prior art date

2014-06-16

Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)

Ceased

Links

• Espacenet
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• -1 Cyanoalkenyl Chemical group 0.000 claims 511
• 150000003254 radicals Chemical class 0.000 claims 226
• 125000004093 cyano group Chemical group *C#N 0.000 claims 202
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 claims 199
• 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims 151
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 138
• 125000004414 alkyl thio group Chemical group 0.000 claims 137
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims 126
• 239000000460 chlorine Chemical group 0.000 claims 124
• 229910052801 chlorine Inorganic materials 0.000 claims 124
• 229910052731 fluorine Inorganic materials 0.000 claims 124
• KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical group ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 claims 123
• 239000011737 fluorine Chemical group 0.000 claims 122
• 229910052736 halogen Chemical group 0.000 claims 122
• 150000002367 halogens Chemical group 0.000 claims 122
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims 114
• 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims 108
• 125000005843 halogen group Chemical group 0.000 claims 103
• 229920006395 saturated elastomer Polymers 0.000 claims 96
• 229910052739 hydrogen Inorganic materials 0.000 claims 94
• 239000001257 hydrogen Substances 0.000 claims 94
• 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims 87
• 125000003118 aryl group Chemical group 0.000 claims 75
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 71
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 66
• 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims 64
• 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims 63
• 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 59
• 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 claims 59
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 58
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 57
• 125000004432 carbon atom Chemical group C* 0.000 claims 52
• 125000006001 difluoroethyl group Chemical group 0.000 claims 52
• 125000004457 alkyl amino carbonyl group Chemical group 0.000 claims 47
• 125000004205 trifluoroethyl group Chemical group [H]C([H])(*)C(F)(F)F 0.000 claims 46
• 229910052757 nitrogen Inorganic materials 0.000 claims 45
• 125000000217 alkyl group Chemical group 0.000 claims 42
• 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 claims 41
• 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims 40
• 125000003545 alkoxy group Chemical group 0.000 claims 40
• 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims 37
• 125000005842 heteroatom Chemical group 0.000 claims 37
• 229910052717 sulfur Inorganic materials 0.000 claims 35
• 125000004750 (C1-C6) alkylaminosulfonyl group Chemical group 0.000 claims 34
• 150000001875 compounds Chemical class 0.000 claims 33
• 229910052760 oxygen Inorganic materials 0.000 claims 33
• 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims 32
• 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 claims 28
• 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims 27
• 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 26
• 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims 25
• 125000005167 cycloalkylaminocarbonyl group Chemical group 0.000 claims 25
• 125000000753 cycloalkyl group Chemical group 0.000 claims 24
• 125000001424 substituent group Chemical group 0.000 claims 24
• 125000001715 oxadiazolyl group Chemical group 0.000 claims 23
• 125000002971 oxazolyl group Chemical group 0.000 claims 23
• 125000003373 pyrazinyl group Chemical group 0.000 claims 23
• 125000003226 pyrazolyl group Chemical group 0.000 claims 23
• 125000002098 pyridazinyl group Chemical group 0.000 claims 23
• 125000000714 pyrimidinyl group Chemical group 0.000 claims 23
• 125000000335 thiazolyl group Chemical group 0.000 claims 23
• 125000004306 triazinyl group Chemical group 0.000 claims 23
• 125000001425 triazolyl group Chemical group 0.000 claims 23
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 22
• 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 claims 22
• 125000000000 cycloalkoxy group Chemical group 0.000 claims 22
• 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims 22
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 22
• 239000003112 inhibitor Substances 0.000 claims 22
• 125000003566 oxetanyl group Chemical group 0.000 claims 22
• 125000005475 oxolanyl group Chemical group 0.000 claims 22
• 125000001412 tetrahydropyranyl group Chemical group 0.000 claims 22
• 125000001072 heteroaryl group Chemical group 0.000 claims 21
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 20
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 20
• 229910052794 bromium Inorganic materials 0.000 claims 20
• 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 19
• 125000005149 cycloalkylsulfinyl group Chemical group 0.000 claims 18
• 125000000392 cycloalkenyl group Chemical group 0.000 claims 17
• 125000003884 phenylalkyl group Chemical group 0.000 claims 17
• 125000006310 cycloalkyl amino group Chemical group 0.000 claims 16
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 claims 15
• 125000004429 atom Chemical group 0.000 claims 14
• 150000002431 hydrogen Chemical class 0.000 claims 14
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 13
• 125000003806 alkyl carbonyl amino group Chemical group 0.000 claims 13
• 125000004656 alkyl sulfonylamino group Chemical group 0.000 claims 13
• 125000005100 aryl amino carbonyl group Chemical group 0.000 claims 13
• 125000001769 aryl amino group Chemical group 0.000 claims 13
• 125000005141 aryl amino sulfonyl group Chemical group 0.000 claims 13
• 125000004658 aryl carbonyl amino group Chemical group 0.000 claims 13
• 125000005162 aryl oxy carbonyl amino group Chemical group 0.000 claims 13
• 125000005161 aryl oxy carbonyl group Chemical group 0.000 claims 13
• 125000005163 aryl sulfanyl group Chemical group 0.000 claims 13
• 125000005135 aryl sulfinyl group Chemical group 0.000 claims 13
• 125000004657 aryl sulfonyl amino group Chemical group 0.000 claims 13
• 125000004391 aryl sulfonyl group Chemical group 0.000 claims 13
• 125000004104 aryloxy group Chemical group 0.000 claims 13
• 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims 13
• 125000005708 carbonyloxy group Chemical group [*:2]OC([*:1])=O 0.000 claims 13
• 125000004986 diarylamino group Chemical group 0.000 claims 13
• 125000004433 nitrogen atom Chemical group N* 0.000 claims 13
• 125000003396 thiol group Chemical group [H]S* 0.000 claims 13
• 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 12
• 125000006269 biphenyl-2-yl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C1=C(*)C([H])=C([H])C([H])=C1[H] 0.000 claims 12
• 239000011593 sulfur Chemical group 0.000 claims 12
• 125000006624 (C1-C6) alkoxycarbonylamino group Chemical group 0.000 claims 11
• 125000006620 amino-(C1-C6) alkyl group Chemical group 0.000 claims 11
• 125000002393 azetidinyl group Chemical group 0.000 claims 11
• 125000004076 pyridyl group Chemical group 0.000 claims 11
• 125000005458 thianyl group Chemical group 0.000 claims 11
• 125000002053 thietanyl group Chemical group 0.000 claims 11
• 125000001166 thiolanyl group Chemical group 0.000 claims 11
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims 10
• IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Substances N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims 10
• 150000002829 nitrogen Chemical class 0.000 claims 10
• 239000001301 oxygen Substances 0.000 claims 10
• 125000004845 (C1-C6) alkylsulfonylamino group Chemical group 0.000 claims 9
• 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims 9
• 125000002252 acyl group Chemical group 0.000 claims 9
• 125000003282 alkyl amino group Chemical group 0.000 claims 9
• 125000005196 alkyl carbonyloxy group Chemical group 0.000 claims 9
• 125000004683 alkyl sulfoxy imino group Chemical group 0.000 claims 9
• 125000001651 cyanato group Chemical group [*]OC#N 0.000 claims 9
• 125000005171 cycloalkylsulfanyl group Chemical group 0.000 claims 9
• 125000005366 cycloalkylthio group Chemical group 0.000 claims 9
• 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims 9
• 125000001113 thiadiazolyl group Chemical group 0.000 claims 9
• ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 9
• 125000004844 (C1-C6) alkoxyimino group Chemical group 0.000 claims 8
• 125000006553 (C3-C8) cycloalkenyl group Chemical group 0.000 claims 8
• 125000005947 C1-C6 alkylsulfonyloxy group Chemical group 0.000 claims 8
• XZMCDFZZKTWFGF-UHFFFAOYSA-N Cyanamide Chemical compound NC#N XZMCDFZZKTWFGF-UHFFFAOYSA-N 0.000 claims 8
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 claims 8
• GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims 8
• 125000005103 alkyl silyl group Chemical group 0.000 claims 8
• 125000001153 fluoro group Chemical group F* 0.000 claims 8
• 239000004480 active ingredient Substances 0.000 claims 7
• 239000000203 mixture Substances 0.000 claims 7
• 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims 6
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims 6
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 6
• 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims 6
• 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 6
• 241000193830 Bacillus <bacterium> Species 0.000 claims 6
• 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims 6
• DFPAKSUCGFBDDF-UHFFFAOYSA-N Nicotinamide Chemical compound NC(=O)C1=CC=CN=C1 DFPAKSUCGFBDDF-UHFFFAOYSA-N 0.000 claims 6
• 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims 6
• 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 6
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 claims 6
• 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 claims 6
• 125000000131 cyclopropyloxy group Chemical group C1(CC1)O* 0.000 claims 6
• 125000003784 fluoroethyl group Chemical group [H]C([H])(F)C([H])([H])* 0.000 claims 6
• 229910052720 vanadium Inorganic materials 0.000 claims 6
• NDOVLWQBFFJETK-UHFFFAOYSA-N 1,4-thiazinane 1,1-dioxide Chemical compound O=S1(=O)CCNCC1 NDOVLWQBFFJETK-UHFFFAOYSA-N 0.000 claims 4
• YHIIJNLSGULWAA-UHFFFAOYSA-N 1,4-thiazinane 1-oxide Chemical compound O=S1CCNCC1 YHIIJNLSGULWAA-UHFFFAOYSA-N 0.000 claims 4
• PVOAHINGSUIXLS-UHFFFAOYSA-N 1-Methylpiperazine Chemical compound CN1CCNCC1 PVOAHINGSUIXLS-UHFFFAOYSA-N 0.000 claims 4
• WGCYRFWNGRMRJA-UHFFFAOYSA-N 1-ethylpiperazine Chemical compound CCN1CCNCC1 WGCYRFWNGRMRJA-UHFFFAOYSA-N 0.000 claims 4
• JXBKZAYVMSNKHA-UHFFFAOYSA-N 1h-tetrazol-1-ium-5-olate Chemical compound OC=1N=NNN=1 JXBKZAYVMSNKHA-UHFFFAOYSA-N 0.000 claims 4
• CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical compound O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 claims 4
• OCVLSHAVSIYKLI-UHFFFAOYSA-N 3h-1,3-thiazole-2-thione Chemical compound SC1=NC=CS1 OCVLSHAVSIYKLI-UHFFFAOYSA-N 0.000 claims 4
• 241000193388 Bacillus thuringiensis Species 0.000 claims 4
• PDQAZBWRQCGBEV-UHFFFAOYSA-N Ethylenethiourea Chemical compound S=C1NCCN1 PDQAZBWRQCGBEV-UHFFFAOYSA-N 0.000 claims 4
• 102000019315 Nicotinic acetylcholine receptors Human genes 0.000 claims 4
• 108050006807 Nicotinic acetylcholine receptors Proteins 0.000 claims 4
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 4
• 125000003342 alkenyl group Chemical group 0.000 claims 4
• 125000004183 alkoxy alkyl group Chemical group 0.000 claims 4
• 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 4
• 229940097012 bacillus thuringiensis Drugs 0.000 claims 4
• 125000004966 cyanoalkyl group Chemical group 0.000 claims 4
• IZBNNCFOBMGTQX-UHFFFAOYSA-N etoperidone Chemical class O=C1N(CC)C(CC)=NN1CCCN1CCN(C=2C=C(Cl)C=CC=2)CC1 IZBNNCFOBMGTQX-UHFFFAOYSA-N 0.000 claims 4
• 229960005437 etoperidone Drugs 0.000 claims 4
• 125000001188 haloalkyl group Chemical group 0.000 claims 4
• 125000002768 hydroxyalkyl group Chemical group 0.000 claims 4
• RONFGUROBZGJKP-UHFFFAOYSA-N iminoctadine Chemical compound NC(N)=NCCCCCCCCNCCCCCCCCN=C(N)N RONFGUROBZGJKP-UHFFFAOYSA-N 0.000 claims 4
• ZVTQYRVARPYRRE-UHFFFAOYSA-N oxadiazol-4-one Chemical compound O=C1CON=N1 ZVTQYRVARPYRRE-UHFFFAOYSA-N 0.000 claims 4
• 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims 4
• HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 claims 4
• QFYXSLAAXZTRLG-UHFFFAOYSA-N pyrrolidine-2,3-dione Chemical compound O=C1CCNC1=O QFYXSLAAXZTRLG-UHFFFAOYSA-N 0.000 claims 4
• IMWUREPEYPRYOR-UHFFFAOYSA-N pyrrolidine-2-thione Chemical compound S=C1CCCN1 IMWUREPEYPRYOR-UHFFFAOYSA-N 0.000 claims 4
• 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 claims 4
• QAJZZLQDLFUNJR-UHFFFAOYSA-N tetrazolidine-5-thione Chemical compound S=C1NNNN1 QAJZZLQDLFUNJR-UHFFFAOYSA-N 0.000 claims 4
• BRNULMACUQOKMR-UHFFFAOYSA-N thiomorpholine Chemical compound C1CSCCN1 BRNULMACUQOKMR-UHFFFAOYSA-N 0.000 claims 4
• YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 claims 3
• OTFNPWZBMHDQHW-UHFFFAOYSA-N 2-(3,3,3-trifluoropropyl)propanedinitrile Chemical compound FC(F)(F)CCC(C#N)C#N OTFNPWZBMHDQHW-UHFFFAOYSA-N 0.000 claims 3
• WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 claims 3
• 125000004105 2-pyridyl group Chemical group N1=C([*])C([H])=C([H])C([H])=C1[H] 0.000 claims 3
• XTDZGXBTXBEZDN-UHFFFAOYSA-N 3-(difluoromethyl)-N-(9-isopropyl-1,2,3,4-tetrahydro-1,4-methanonaphthalen-5-yl)-1-methylpyrazole-4-carboxamide Chemical compound CC(C)C1C2CCC1C1=C2C=CC=C1NC(=O)C1=CN(C)N=C1C(F)F XTDZGXBTXBEZDN-UHFFFAOYSA-N 0.000 claims 3
• 125000003349 3-pyridyl group Chemical group N1=C([H])C([*])=C([H])C([H])=C1[H] 0.000 claims 3
• LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims 3
• 239000005799 Isopyrazam Substances 0.000 claims 3
• LGDSHSYDSCRFAB-UHFFFAOYSA-N Methyl isothiocyanate Chemical compound CN=C=S LGDSHSYDSCRFAB-UHFFFAOYSA-N 0.000 claims 3
• YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims 3
• MKIMSXGUTQTKJU-UHFFFAOYSA-N Propamocarb hydrochloride Chemical compound [Cl-].CCCOC(=O)NCCC[NH+](C)C MKIMSXGUTQTKJU-UHFFFAOYSA-N 0.000 claims 3
• 241000607479 Yersinia pestis Species 0.000 claims 3
• DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 claims 3
• 239000002253 acid Substances 0.000 claims 3
• 239000012872 agrochemical composition Substances 0.000 claims 3
• 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 claims 3
• 125000004471 alkyl aminosulfonyl group Chemical group 0.000 claims 3
• 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 claims 3
• 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 3
• 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 claims 3
• 230000015572 biosynthetic process Effects 0.000 claims 3
• TWFZGCMQGLPBSX-UHFFFAOYSA-N carbendazim Chemical compound C1=CC=C2NC(NC(=O)OC)=NC2=C1 TWFZGCMQGLPBSX-UHFFFAOYSA-N 0.000 claims 3
• 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 3
• 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 3
• 125000004472 dialkylaminosulfonyl group Chemical group 0.000 claims 3
• 125000004671 dialkylaminothiocarbonyl group Chemical group 0.000 claims 3
• 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 claims 3
• DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 claims 3
• NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims 3
• KVDJTXBXMWJJEF-UHFFFAOYSA-N fluopyram Chemical compound ClC1=CC(C(F)(F)F)=CN=C1CCNC(=O)C1=CC=CC=C1C(F)(F)F KVDJTXBXMWJJEF-UHFFFAOYSA-N 0.000 claims 3
• 125000004438 haloalkoxy group Chemical group 0.000 claims 3
• 125000004993 haloalkoxycarbonyl group Chemical group 0.000 claims 3
• 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims 3
• 125000004440 haloalkylsulfinyl group Chemical group 0.000 claims 3
• 125000001841 imino group Chemical group [H]N=* 0.000 claims 3
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 3
• 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims 3
• 235000005152 nicotinamide Nutrition 0.000 claims 3
• 239000011570 nicotinamide Substances 0.000 claims 3
• 125000005359 phenoxyalkyl group Chemical group 0.000 claims 3
• QJBZDBLBQWFTPZ-UHFFFAOYSA-N pyrrolnitrin Chemical compound [O-][N+](=O)C1=C(Cl)C=CC=C1C1=CNC=C1Cl QJBZDBLBQWFTPZ-UHFFFAOYSA-N 0.000 claims 3
• MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims 3
• FBQQHUGEACOBDN-UHFFFAOYSA-N quinomethionate Chemical compound N1=C2SC(=O)SC2=NC2=CC(C)=CC=C21 FBQQHUGEACOBDN-UHFFFAOYSA-N 0.000 claims 3
• 230000035806 respiratory chain Effects 0.000 claims 3
• 150000003839 salts Chemical class 0.000 claims 3
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims 3
• AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 claims 3
• CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 claims 2
• YNWVFADWVLCOPU-MDWZMJQESA-N (1E)-1-(4-chlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol Chemical compound C1=NC=NN1/C(C(O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1 YNWVFADWVLCOPU-MDWZMJQESA-N 0.000 claims 2
• 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 claims 2
• SBNFWQZLDJGRLK-RTWAWAEBSA-N (1R)-trans-phenothrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 SBNFWQZLDJGRLK-RTWAWAEBSA-N 0.000 claims 2
• ZMYFCFLJBGAQRS-IAGOWNOFSA-N (2S,3R)-epoxiconazole Chemical compound C1=CC(F)=CC=C1[C@]1(CN2N=CN=C2)[C@@H](C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-IAGOWNOFSA-N 0.000 claims 2
• 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 claims 2
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