BRPI0416200B1 - Carboxamidas sililadas, seu processo de preparação e seu emprego, agente e seu processo de preparação , e processo para combate de microorganismos indesejados - Google Patents

Info

Publication number

BRPI0416200B1

BRPI0416200B1 BRPI0416200-5A BRPI0416200A BRPI0416200B1 BR PI0416200 B1 BRPI0416200 B1 BR PI0416200B1 BR PI0416200 A BRPI0416200 A BR PI0416200A BR PI0416200 B1 BRPI0416200 B1 BR PI0416200B1

Authority

BR

Brazil

Prior art keywords

alkyl

formula

methyl

plants

particularly preferred

Prior art date

2003-11-21

Links

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• Global Dossier
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• 238000000034 method Methods 0.000 title claims description 31
• 244000005700 microbiome Species 0.000 title claims description 19
• 150000003857 carboxamides Chemical class 0.000 title claims description 16
• 238000002360 preparation method Methods 0.000 title description 20
• 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 38
• 239000001257 hydrogen Substances 0.000 claims description 30
• 229910052739 hydrogen Inorganic materials 0.000 claims description 30
• 239000011737 fluorine Chemical group 0.000 claims description 23
• 229910052731 fluorine Chemical group 0.000 claims description 23
• PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical group FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 22
• 229910052736 halogen Inorganic materials 0.000 claims description 14
• 239000003795 chemical substances by application Substances 0.000 claims description 10
• 239000002253 acid Substances 0.000 claims description 9
• 150000002367 halogens Chemical class 0.000 claims description 9
• 150000001412 amines Chemical class 0.000 claims description 8
• 150000001732 carboxylic acid derivatives Chemical class 0.000 claims description 5
• 239000003085 diluting agent Substances 0.000 claims description 4
• 239000004604 Blowing Agent Substances 0.000 claims description 3
• 239000011230 binding agent Substances 0.000 claims description 3
• 238000007664 blowing Methods 0.000 claims description 3
• 239000003054 catalyst Substances 0.000 claims description 3
• 238000004519 manufacturing process Methods 0.000 claims description 3
• 239000004094 surface-active agent Substances 0.000 claims description 3
• 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 2
• 241001465754 Metazoa Species 0.000 claims 2
• 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
• -1 C 2 -C 6 haloalkyl Chemical group 0.000 description 112
• 241000196324 Embryophyta Species 0.000 description 73
• 125000000217 alkyl group Chemical group 0.000 description 42
• 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 38
• 239000013543 active substance Substances 0.000 description 36
• KZBUYRJDOAKODT-UHFFFAOYSA-N Chlorine Chemical group ClCl KZBUYRJDOAKODT-UHFFFAOYSA-N 0.000 description 26
• 239000000460 chlorine Chemical group 0.000 description 26
• 229910052801 chlorine Inorganic materials 0.000 description 26
• 150000002431 hydrogen Chemical group 0.000 description 25
• 150000003254 radicals Chemical class 0.000 description 24
• 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 23
• 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 23
• 125000003545 alkoxy group Chemical group 0.000 description 21
• 125000001246 bromo group Chemical group Br* 0.000 description 21
• 150000001875 compounds Chemical class 0.000 description 18
• 125000005843 halogen group Chemical group 0.000 description 18
• 239000000463 material Substances 0.000 description 18
• 239000000203 mixture Substances 0.000 description 18
• RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 17
• 125000001153 fluoro group Chemical group F* 0.000 description 17
• WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 16
• GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 16
• 229910052794 bromium Inorganic materials 0.000 description 16
• WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 15
• YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 15
• 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 15
• XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 14
• ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 13
• 125000001309 chloro group Chemical group Cl* 0.000 description 13
• HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 12
• YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 12
• 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 12
• 239000002904 solvent Substances 0.000 description 12
• 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 12
• 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 11
• 241000233866 Fungi Species 0.000 description 11
• 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 description 11
• 125000000623 heterocyclic group Chemical group 0.000 description 11
• 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 11
• 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 11
• 240000008042 Zea mays Species 0.000 description 10
• 235000002017 Zea mays subsp mays Nutrition 0.000 description 10
• HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 9
• ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
• 239000003995 emulsifying agent Substances 0.000 description 9
• 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 9
• 229910052757 nitrogen Inorganic materials 0.000 description 9
• 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 8
• 229920000742 Cotton Polymers 0.000 description 8
• 244000299507 Gossypium hirsutum Species 0.000 description 8
• NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 8
• 125000001188 haloalkyl group Chemical group 0.000 description 8
• 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 8
• 125000004433 nitrogen atom Chemical group N* 0.000 description 8
• BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 8
• 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 8
• 229910052717 sulfur Inorganic materials 0.000 description 8
• 239000011593 sulfur Substances 0.000 description 8
• QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 7
• 238000009472 formulation Methods 0.000 description 7
• 239000001301 oxygen Substances 0.000 description 7
• 229910052760 oxygen Inorganic materials 0.000 description 7
• 239000002689 soil Substances 0.000 description 7
• 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 description 6
• CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
• UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
• 235000010469 Glycine max Nutrition 0.000 description 6
• SJRJJKPEHAURKC-UHFFFAOYSA-N N-Methylmorpholine Chemical compound CN1CCOCC1 SJRJJKPEHAURKC-UHFFFAOYSA-N 0.000 description 6
• GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 6
• KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 6
• 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 6
• 238000006243 chemical reaction Methods 0.000 description 6
• 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 6
• 235000009973 maize Nutrition 0.000 description 6
• 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 6
• UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 6
• VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 6
• 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 6
• 239000000843 powder Substances 0.000 description 6
• 239000007858 starting material Substances 0.000 description 6
• 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 description 5
• 241000894006 Bacteria Species 0.000 description 5
• XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 5
• 241000700605 Viruses Species 0.000 description 5
• 239000000969 carrier Substances 0.000 description 5
• 230000002363 herbicidal effect Effects 0.000 description 5
• 239000004009 herbicide Substances 0.000 description 5
• 125000005842 heteroatom Chemical group 0.000 description 5
• 239000000047 product Substances 0.000 description 5
• 230000009261 transgenic effect Effects 0.000 description 5
• 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 4
• 125000004771 (C1-C4) haloalkylsulfinyl group Chemical group 0.000 description 4
• UOCLXMDMGBRAIB-UHFFFAOYSA-N 1,1,1-trichloroethane Chemical compound CC(Cl)(Cl)Cl UOCLXMDMGBRAIB-UHFFFAOYSA-N 0.000 description 4
• NFDXQGNDWIPXQL-UHFFFAOYSA-N 1-cyclooctyldiazocane Chemical compound C1CCCCCCC1N1NCCCCCC1 NFDXQGNDWIPXQL-UHFFFAOYSA-N 0.000 description 4
• PAMIQIKDUOTOBW-UHFFFAOYSA-N 1-methylpiperidine Chemical compound CN1CCCCC1 PAMIQIKDUOTOBW-UHFFFAOYSA-N 0.000 description 4
• ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 4
• RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
• XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 4
• QOSSAOTZNIDXMA-UHFFFAOYSA-N Dicylcohexylcarbodiimide Chemical compound C1CCCCC1N=C=NC1CCCCC1 QOSSAOTZNIDXMA-UHFFFAOYSA-N 0.000 description 4
• XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 4
• 244000068988 Glycine max Species 0.000 description 4
• YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 4
• IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
• 241000221300 Puccinia Species 0.000 description 4
• JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 4
• CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
• UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
• WQDUMFSSJAZKTM-UHFFFAOYSA-N Sodium methoxide Chemical compound [Na+].[O-]C WQDUMFSSJAZKTM-UHFFFAOYSA-N 0.000 description 4
• 244000061456 Solanum tuberosum Species 0.000 description 4
• 235000002595 Solanum tuberosum Nutrition 0.000 description 4
• WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 4
• 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
• 125000002877 alkyl aryl group Chemical group 0.000 description 4
• 150000001408 amides Chemical class 0.000 description 4
• RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical compound COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 description 4
• MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 4
• 239000010949 copper Substances 0.000 description 4
• 229910052802 copper Inorganic materials 0.000 description 4
• 235000005822 corn Nutrition 0.000 description 4
• NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 4
• 239000012973 diazabicyclooctane Substances 0.000 description 4
• 125000005745 ethoxymethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])* 0.000 description 4
• 239000000417 fungicide Substances 0.000 description 4
• 239000007789 gas Substances 0.000 description 4
• 239000008187 granular material Substances 0.000 description 4
• 150000004820 halides Chemical class 0.000 description 4
• 125000004356 hydroxy functional group Chemical group O* 0.000 description 4
• 238000011081 inoculation Methods 0.000 description 4
• 239000011630 iodine Substances 0.000 description 4
• 229910052740 iodine Inorganic materials 0.000 description 4
• 239000007788 liquid Substances 0.000 description 4
• ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 4
• 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 description 4
• 239000003208 petroleum Substances 0.000 description 4
• SCVFZCLFOSHCOH-UHFFFAOYSA-M potassium acetate Chemical compound [K+].CC([O-])=O SCVFZCLFOSHCOH-UHFFFAOYSA-M 0.000 description 4
• 229910000027 potassium carbonate Inorganic materials 0.000 description 4
• 235000011181 potassium carbonates Nutrition 0.000 description 4
• 239000002243 precursor Substances 0.000 description 4
• 230000001012 protector Effects 0.000 description 4
• 108090000623 proteins and genes Proteins 0.000 description 4
• 125000006413 ring segment Chemical group 0.000 description 4
• 241000894007 species Species 0.000 description 4
• 238000005507 spraying Methods 0.000 description 4
• 239000000725 suspension Substances 0.000 description 4
• GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 4
• ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
• 241000223600 Alternaria Species 0.000 description 3
• 240000002791 Brassica napus Species 0.000 description 3
• 235000004977 Brassica sinapistrum Nutrition 0.000 description 3
• UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 3
• 235000011430 Malus pumila Nutrition 0.000 description 3
• 235000015103 Malus silvestris Nutrition 0.000 description 3
• PAYRUJLWNCNPSJ-UHFFFAOYSA-N N-phenyl amine Natural products NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 3
• 244000061176 Nicotiana tabacum Species 0.000 description 3
• 235000002637 Nicotiana tabacum Nutrition 0.000 description 3
• CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 3
• 241000317942 Venturia <ichneumonid wasp> Species 0.000 description 3
• 239000000853 adhesive Substances 0.000 description 3
• 230000001070 adhesive effect Effects 0.000 description 3
• 230000000844 anti-bacterial effect Effects 0.000 description 3
• 239000003899 bactericide agent Substances 0.000 description 3
• JFDZBHWFFUWGJE-UHFFFAOYSA-N benzonitrile Chemical compound N#CC1=CC=CC=C1 JFDZBHWFFUWGJE-UHFFFAOYSA-N 0.000 description 3
• 235000013339 cereals Nutrition 0.000 description 3
• 238000004440 column chromatography Methods 0.000 description 3
• 239000012141 concentrate Substances 0.000 description 3
• 244000038559 crop plants Species 0.000 description 3
• 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 3
• 230000006735 deficit Effects 0.000 description 3
• IJKVHSBPTUYDLN-UHFFFAOYSA-N dihydroxy(oxo)silane Chemical compound O[Si](O)=O IJKVHSBPTUYDLN-UHFFFAOYSA-N 0.000 description 3
• 238000010410 dusting Methods 0.000 description 3
• 239000000975 dye Substances 0.000 description 3
• 235000013399 edible fruits Nutrition 0.000 description 3
• 150000002170 ethers Chemical class 0.000 description 3
• 125000005448 ethoxyethyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])* 0.000 description 3
• 238000011156 evaluation Methods 0.000 description 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 description 3
• 235000013305 food Nutrition 0.000 description 3
• XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 description 3
• GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 3
• 230000003641 microbiacidal effect Effects 0.000 description 3
• 238000002156 mixing Methods 0.000 description 3
• 239000003960 organic solvent Substances 0.000 description 3
• 230000008635 plant growth Effects 0.000 description 3
• TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 3
• 230000001681 protective effect Effects 0.000 description 3
• 238000000746 purification Methods 0.000 description 3
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• 238000001228 spectrum Methods 0.000 description 3
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• 238000003860 storage Methods 0.000 description 3
• 238000012360 testing method Methods 0.000 description 3
• VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 3
• 239000002023 wood Substances 0.000 description 3
• 239000008096 xylene Substances 0.000 description 3
• JLYXXMFPNIAWKQ-UHFFFAOYSA-N γ Benzene hexachloride Chemical compound ClC1C(Cl)C(Cl)C(Cl)C(Cl)C1Cl JLYXXMFPNIAWKQ-UHFFFAOYSA-N 0.000 description 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 description 2
• 125000004455 (C1-C3) alkylthio group Chemical group 0.000 description 2
• 125000004768 (C1-C4) alkylsulfinyl group Chemical group 0.000 description 2
• 125000004769 (C1-C4) alkylsulfonyl group Chemical group 0.000 description 2
• 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 description 2
• 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 description 2
• 125000004737 (C1-C6) haloalkoxy group Chemical group 0.000 description 2
• SCYULBFZEHDVBN-UHFFFAOYSA-N 1,1-Dichloroethane Chemical compound CC(Cl)Cl SCYULBFZEHDVBN-UHFFFAOYSA-N 0.000 description 2
• LZDKZFUFMNSQCJ-UHFFFAOYSA-N 1,2-diethoxyethane Chemical compound CCOCCOCC LZDKZFUFMNSQCJ-UHFFFAOYSA-N 0.000 description 2
• RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 2
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• QSRRWODNHOIZLD-UHFFFAOYSA-N 2-(2-trimethylsilylethyl)aniline Chemical compound C[Si](C)(C)CCC1=CC=CC=C1N QSRRWODNHOIZLD-UHFFFAOYSA-N 0.000 description 2
• WNZQDUSMALZDQF-UHFFFAOYSA-N 2-benzofuran-1(3H)-one Chemical compound C1=CC=C2C(=O)OCC2=C1 WNZQDUSMALZDQF-UHFFFAOYSA-N 0.000 description 2
• CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 2
• SWBHWUYHHJCADA-UHFFFAOYSA-N 3-(2-chlorophenyl)-6-(2,6-difluorophenyl)-1,2,4,5-tetrazine Chemical compound FC1=CC=CC(F)=C1C1=NN=C(C=2C(=CC=CC=2)Cl)N=N1 SWBHWUYHHJCADA-UHFFFAOYSA-N 0.000 description 2
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• 239000005660 Abamectin Substances 0.000 description 2
• XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
• 241000228212 Aspergillus Species 0.000 description 2
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• 241000221198 Basidiomycota Species 0.000 description 2
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• IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
• GKQLYSROISKDLL-UHFFFAOYSA-N EEDQ Chemical compound C1=CC=C2N(C(=O)OCC)C(OCC)C=CC2=C1 GKQLYSROISKDLL-UHFFFAOYSA-N 0.000 description 2
• 239000005894 Emamectin Substances 0.000 description 2
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