DE3779814T2 - Insektentoetende n-substituierte-n'-substituierte-n,n'-diacylhydrazine. - Google Patents
Insektentoetende n-substituierte-n'-substituierte-n,n'-diacylhydrazine.Info
- Publication number
- DE3779814T2 DE3779814T2 DE8787303092T DE3779814T DE3779814T2 DE 3779814 T2 DE3779814 T2 DE 3779814T2 DE 8787303092 T DE8787303092 T DE 8787303092T DE 3779814 T DE3779814 T DE 3779814T DE 3779814 T2 DE3779814 T2 DE 3779814T2
- Authority
- DE
- Germany
- Prior art keywords
- alkyl
- hydrazine
- radical
- butyl
- alkoxy
- Prior art date
- 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.)
- Expired - Fee Related
Links
- 229910052757 nitrogen Inorganic materials 0.000 title description 15
- 150000001875 compounds Chemical class 0.000 claims description 98
- -1 alkyl radical Chemical class 0.000 claims description 97
- 239000000203 mixture Substances 0.000 claims description 75
- 238000000034 method Methods 0.000 claims description 67
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims description 61
- 229910052736 halogen Inorganic materials 0.000 claims description 54
- 150000002367 halogens Chemical class 0.000 claims description 54
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 47
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 claims description 46
- OAKJQQAXSVQMHS-UHFFFAOYSA-N hydrazine Substances NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 38
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims description 28
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 28
- 125000004423 acyloxy group Chemical group 0.000 claims description 27
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 26
- 150000003839 salts Chemical class 0.000 claims description 25
- 125000004432 carbon atom Chemical group C* 0.000 claims description 24
- 241000238631 Hexapoda Species 0.000 claims description 22
- 239000003795 chemical substances by application Substances 0.000 claims description 21
- 230000000749 insecticidal effect Effects 0.000 claims description 21
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 21
- 125000001424 substituent group Chemical group 0.000 claims description 20
- 239000007788 liquid Substances 0.000 claims description 15
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 claims description 12
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims description 11
- 239000008187 granular material Substances 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 239000001257 hydrogen Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 9
- 229910052760 oxygen Inorganic materials 0.000 claims description 9
- 125000006730 (C2-C5) alkynyl group Chemical group 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 8
- 125000004414 alkyl thio group Chemical group 0.000 claims description 8
- 150000002429 hydrazines Chemical class 0.000 claims description 8
- 239000002270 dispersing agent Substances 0.000 claims description 7
- 239000004495 emulsifiable concentrate Substances 0.000 claims description 7
- 239000003995 emulsifying agent Substances 0.000 claims description 7
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims description 6
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 claims description 6
- 241000255777 Lepidoptera Species 0.000 claims description 6
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- 239000003085 diluting agent Substances 0.000 claims description 6
- 230000009969 flowable effect Effects 0.000 claims description 6
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 6
- 125000001624 naphthyl group Chemical group 0.000 claims description 6
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
- 125000000858 thiocyanato group Chemical group *SC#N 0.000 claims description 6
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims description 5
- 239000000460 chlorine Substances 0.000 claims description 5
- 229910052801 chlorine Inorganic materials 0.000 claims description 5
- 239000000428 dust Substances 0.000 claims description 5
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 5
- 125000006729 (C2-C5) alkenyl group Chemical group 0.000 claims description 4
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 4
- 241000254173 Coleoptera Species 0.000 claims description 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 claims description 4
- 125000005103 alkyl silyl group Chemical group 0.000 claims description 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 4
- 229910052794 bromium Inorganic materials 0.000 claims description 4
- 239000011737 fluorine Substances 0.000 claims description 4
- 229910052731 fluorine Inorganic materials 0.000 claims description 4
- 125000005843 halogen group Chemical group 0.000 claims description 4
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims description 4
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 4
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 claims description 3
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 claims description 3
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 3
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 claims description 3
- 125000000623 heterocyclic group Chemical group 0.000 claims description 3
- XOZTUTRCCSSMHM-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-(4-methylbenzoyl)-n'-(phenylsulfanylmethyl)benzohydrazide Chemical compound C1=CC(C)=CC=C1C(=O)N(N(C(=O)C=1C=C(Cl)C(Cl)=CC=1)C(C)(C)C)CSC1=CC=CC=C1 XOZTUTRCCSSMHM-UHFFFAOYSA-N 0.000 claims description 3
- 239000004563 wettable powder Substances 0.000 claims description 3
- 125000005919 1,2,2-trimethylpropyl group Chemical group 0.000 claims description 2
- 125000004399 C1-C4 alkenyl group Chemical group 0.000 claims description 2
- 125000005090 alkenylcarbonyl group Chemical group 0.000 claims description 2
- 125000005083 alkoxyalkoxy group Chemical group 0.000 claims description 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 claims description 2
- 125000005087 alkynylcarbonyl group Chemical group 0.000 claims description 2
- 125000002490 anilino group Chemical group [H]N(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 239000005667 attractant Substances 0.000 claims description 2
- 230000031902 chemoattractant activity Effects 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 claims description 2
- 125000004092 methylthiomethyl group Chemical group [H]C([H])([H])SC([H])([H])* 0.000 claims description 2
- 125000000018 nitroso group Chemical group N(=O)* 0.000 claims description 2
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 claims description 2
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 claims description 2
- 125000003396 thiol group Chemical group [H]S* 0.000 claims description 2
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000006772 (C1-C6) haloalkylsulfonyloxy group Chemical group 0.000 claims 1
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 claims 1
- 125000001494 2-propynyl group Chemical group [H]C#CC([H])([H])* 0.000 claims 1
- 125000004189 3,4-dichlorophenyl group Chemical group [H]C1=C([H])C(Cl)=C(Cl)C([H])=C1* 0.000 claims 1
- YNPNZTXNASCQKK-UHFFFAOYSA-N Phenanthrene Natural products C1=CC=C2C3=CC=CC=C3C=CC2=C1 YNPNZTXNASCQKK-UHFFFAOYSA-N 0.000 claims 1
- DGEZNRSVGBDHLK-UHFFFAOYSA-N [1,10]phenanthroline Chemical compound C1=CN=C2C3=NC=CC=C3C=CC2=C1 DGEZNRSVGBDHLK-UHFFFAOYSA-N 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims 1
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 57
- 239000002904 solvent Substances 0.000 description 57
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 45
- 230000008569 process Effects 0.000 description 42
- 238000002360 preparation method Methods 0.000 description 35
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 33
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 33
- 239000002585 base Substances 0.000 description 33
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 30
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 29
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 27
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 26
- 150000003254 radicals Chemical class 0.000 description 22
- 238000009472 formulation Methods 0.000 description 16
- 239000000243 solution Substances 0.000 description 16
- 239000000126 substance Substances 0.000 description 16
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 15
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 15
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 14
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 description 14
- 239000007921 spray Substances 0.000 description 14
- 241000196324 Embryophyta Species 0.000 description 13
- 239000002253 acid Substances 0.000 description 13
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 13
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 12
- 239000007787 solid Substances 0.000 description 12
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 11
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 11
- 241000607479 Yersinia pestis Species 0.000 description 11
- 150000001298 alcohols Chemical class 0.000 description 11
- 239000000969 carrier Substances 0.000 description 11
- 239000003054 catalyst Substances 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 10
- 239000013543 active substance Substances 0.000 description 10
- 150000002170 ethers Chemical class 0.000 description 10
- 239000012442 inert solvent Substances 0.000 description 10
- 238000012360 testing method Methods 0.000 description 10
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 9
- XTHFKEDIFFGKHM-UHFFFAOYSA-N Dimethoxyethane Chemical compound COCCOC XTHFKEDIFFGKHM-UHFFFAOYSA-N 0.000 description 9
- ZMANZCXQSJIPKH-UHFFFAOYSA-N Triethylamine Chemical compound CCN(CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-N 0.000 description 9
- 239000002917 insecticide Substances 0.000 description 9
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 9
- 239000000843 powder Substances 0.000 description 9
- 239000000376 reactant Substances 0.000 description 9
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 8
- DTQVDTLACAAQTR-UHFFFAOYSA-N Trifluoroacetic acid Chemical compound OC(=O)C(F)(F)F DTQVDTLACAAQTR-UHFFFAOYSA-N 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 8
- 231100000614 poison Toxicity 0.000 description 8
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000002574 poison Substances 0.000 description 7
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 7
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 6
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 6
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
- KEAYESYHFKHZAL-UHFFFAOYSA-N Sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 6
- 125000004356 hydroxy functional group Chemical group O* 0.000 description 6
- 229910052751 metal Inorganic materials 0.000 description 6
- 239000002184 metal Substances 0.000 description 6
- 239000003921 oil Substances 0.000 description 6
- 239000004533 oil dispersion Substances 0.000 description 6
- 235000019198 oils Nutrition 0.000 description 6
- 239000001301 oxygen Substances 0.000 description 6
- 239000000047 product Substances 0.000 description 6
- 239000011541 reaction mixture Substances 0.000 description 6
- 229910000104 sodium hydride Inorganic materials 0.000 description 6
- 239000012312 sodium hydride Substances 0.000 description 6
- 238000005507 spraying Methods 0.000 description 6
- 239000004094 surface-active agent Substances 0.000 description 6
- NISLLQUWIJASOV-UHFFFAOYSA-N N'-benzoyl-N-(tert-butyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)(C)C)NC(=O)C1=CC=CC=C1 NISLLQUWIJASOV-UHFFFAOYSA-N 0.000 description 5
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 5
- 235000011054 acetic acid Nutrition 0.000 description 5
- 150000007513 acids Chemical class 0.000 description 5
- 150000003863 ammonium salts Chemical class 0.000 description 5
- 239000012876 carrier material Substances 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 239000003638 chemical reducing agent Substances 0.000 description 5
- 229930195733 hydrocarbon Natural products 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 229910052500 inorganic mineral Inorganic materials 0.000 description 5
- 239000010410 layer Substances 0.000 description 5
- 238000004519 manufacturing process Methods 0.000 description 5
- 239000011707 mineral Substances 0.000 description 5
- 235000010755 mineral Nutrition 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 230000000361 pesticidal effect Effects 0.000 description 5
- 239000007858 starting material Substances 0.000 description 5
- 239000008096 xylene Substances 0.000 description 5
- GRRIYLZJLGTQJX-UHFFFAOYSA-N 1,2-dibenzoylhydrazine Chemical class C=1C=CC=CC=1C(=O)NNC(=O)C1=CC=CC=C1 GRRIYLZJLGTQJX-UHFFFAOYSA-N 0.000 description 4
- 241001477931 Mythimna unipuncta Species 0.000 description 4
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 4
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 4
- 240000008042 Zea mays Species 0.000 description 4
- 235000005824 Zea mays ssp. parviglumis Nutrition 0.000 description 4
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 4
- 230000002411 adverse Effects 0.000 description 4
- 150000004703 alkoxides Chemical class 0.000 description 4
- 235000005822 corn Nutrition 0.000 description 4
- 235000014113 dietary fatty acids Nutrition 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 239000000194 fatty acid Substances 0.000 description 4
- 229930195729 fatty acid Natural products 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- HQKMJHAJHXVSDF-UHFFFAOYSA-L magnesium stearate Chemical compound [Mg+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O HQKMJHAJHXVSDF-UHFFFAOYSA-L 0.000 description 4
- 238000012986 modification Methods 0.000 description 4
- 230000004048 modification Effects 0.000 description 4
- 150000007524 organic acids Chemical class 0.000 description 4
- 235000005985 organic acids Nutrition 0.000 description 4
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 description 3
- RYHBNJHYFVUHQT-UHFFFAOYSA-N 1,4-Dioxane Chemical compound C1COCCO1 RYHBNJHYFVUHQT-UHFFFAOYSA-N 0.000 description 3
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 3
- 241001388466 Bruchus rufimanus Species 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 3
- 239000002671 adjuvant Substances 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 150000001350 alkyl halides Chemical class 0.000 description 3
- 235000012211 aluminium silicate Nutrition 0.000 description 3
- 150000001412 amines Chemical class 0.000 description 3
- 125000004966 cyanoalkyl group Chemical group 0.000 description 3
- 239000006185 dispersion Substances 0.000 description 3
- 239000000975 dye Substances 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 150000002576 ketones Chemical class 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 229910052987 metal hydride Inorganic materials 0.000 description 3
- 150000004681 metal hydrides Chemical class 0.000 description 3
- GPKWTMLPXWDXMK-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n-(methoxymethyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(COC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 GPKWTMLPXWDXMK-UHFFFAOYSA-N 0.000 description 3
- LTVYAZDGHANPJT-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1 LTVYAZDGHANPJT-UHFFFAOYSA-N 0.000 description 3
- VHKSSHDISGKMRJ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3,5-dimethyl-n'-prop-2-ynylbenzohydrazide Chemical compound CC1=CC(C)=CC(C(=O)N(N(CC#C)C(=O)C=2C=CC=CC=2)C(C)(C)C)=C1 VHKSSHDISGKMRJ-UHFFFAOYSA-N 0.000 description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 description 3
- 239000003960 organic solvent Substances 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 239000006072 paste Substances 0.000 description 3
- 239000002243 precursor Substances 0.000 description 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 3
- 239000003380 propellant Substances 0.000 description 3
- 239000002002 slurry Substances 0.000 description 3
- 239000002689 soil Substances 0.000 description 3
- 239000011593 sulfur Substances 0.000 description 3
- 239000000454 talc Substances 0.000 description 3
- 229910052623 talc Inorganic materials 0.000 description 3
- 235000012222 talc Nutrition 0.000 description 3
- 239000012085 test solution Substances 0.000 description 3
- 231100000331 toxic Toxicity 0.000 description 3
- 231100000167 toxic agent Toxicity 0.000 description 3
- 230000002588 toxic effect Effects 0.000 description 3
- 239000003440 toxic substance Substances 0.000 description 3
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 3
- QWLQTDXXEZQUBB-UHFFFAOYSA-N 1,2-di(propan-2-yl)hydrazine Chemical compound CC(C)NNC(C)C QWLQTDXXEZQUBB-UHFFFAOYSA-N 0.000 description 2
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
- QCQCHGYLTSGIGX-GHXANHINSA-N 4-[[(3ar,5ar,5br,7ar,9s,11ar,11br,13as)-5a,5b,8,8,11a-pentamethyl-3a-[(5-methylpyridine-3-carbonyl)amino]-2-oxo-1-propan-2-yl-4,5,6,7,7a,9,10,11,11b,12,13,13a-dodecahydro-3h-cyclopenta[a]chrysen-9-yl]oxy]-2,2-dimethyl-4-oxobutanoic acid Chemical compound N([C@@]12CC[C@@]3(C)[C@]4(C)CC[C@H]5C(C)(C)[C@@H](OC(=O)CC(C)(C)C(O)=O)CC[C@]5(C)[C@H]4CC[C@@H]3C1=C(C(C2)=O)C(C)C)C(=O)C1=CN=CC(C)=C1 QCQCHGYLTSGIGX-GHXANHINSA-N 0.000 description 2
- 239000005995 Aluminium silicate Substances 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical class [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- 239000005909 Kieselgur Substances 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- 229910002651 NO3 Inorganic materials 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
- 244000061176 Nicotiana tabacum Species 0.000 description 2
- 235000002637 Nicotiana tabacum Nutrition 0.000 description 2
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 2
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 241001521235 Spodoptera eridania Species 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 235000011941 Tilia x europaea Nutrition 0.000 description 2
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 125000000304 alkynyl group Chemical group 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 229960000892 attapulgite Drugs 0.000 description 2
- 239000000440 bentonite Substances 0.000 description 2
- 229910000278 bentonite Inorganic materials 0.000 description 2
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- PASDCCFISLVPSO-UHFFFAOYSA-N benzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1 PASDCCFISLVPSO-UHFFFAOYSA-N 0.000 description 2
- 239000011230 binding agent Substances 0.000 description 2
- 230000004071 biological effect Effects 0.000 description 2
- 238000009835 boiling Methods 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 239000003086 colorant Substances 0.000 description 2
- 238000002485 combustion reaction Methods 0.000 description 2
- 235000005687 corn oil Nutrition 0.000 description 2
- 239000002285 corn oil Substances 0.000 description 2
- JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 239000010459 dolomite Substances 0.000 description 2
- 229910000514 dolomite Inorganic materials 0.000 description 2
- 238000010410 dusting Methods 0.000 description 2
- 235000013399 edible fruits Nutrition 0.000 description 2
- 239000012530 fluid Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 125000000524 functional group Chemical group 0.000 description 2
- 239000000417 fungicide Substances 0.000 description 2
- 125000001188 haloalkyl group Chemical group 0.000 description 2
- 150000008282 halocarbons Chemical class 0.000 description 2
- 150000004678 hydrides Chemical class 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 2
- HJOVHMDZYOCNQW-UHFFFAOYSA-N isophorone Chemical compound CC1=CC(=O)CC(C)(C)C1 HJOVHMDZYOCNQW-UHFFFAOYSA-N 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 2
- 231100000518 lethal Toxicity 0.000 description 2
- 230000001665 lethal effect Effects 0.000 description 2
- 239000004571 lime Substances 0.000 description 2
- 239000012280 lithium aluminium hydride Substances 0.000 description 2
- ZCSHNCUQKCANBX-UHFFFAOYSA-N lithium diisopropylamide Chemical compound [Li+].CC(C)[N-]C(C)C ZCSHNCUQKCANBX-UHFFFAOYSA-N 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 235000019359 magnesium stearate Nutrition 0.000 description 2
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 2
- 229910000000 metal hydroxide Inorganic materials 0.000 description 2
- 150000004692 metal hydroxides Chemical class 0.000 description 2
- QNTKMJGJEUWGLG-UHFFFAOYSA-N n'-benzoyl-n'-cyclohexylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)NN(C(=O)C=1C=CC=CC=1)C1CCCCC1 QNTKMJGJEUWGLG-UHFFFAOYSA-N 0.000 description 2
- PFGAKEHPUFHLAQ-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n-(methylsulfanylmethyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CSC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 PFGAKEHPUFHLAQ-UHFFFAOYSA-N 0.000 description 2
- XCNCLAVUNAOXJL-UHFFFAOYSA-N n'-benzoyl-n-benzyl-n'-tert-butylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)(C)C)N(C(=O)C=1C=CC=CC=1)CC1=CC=CC=C1 XCNCLAVUNAOXJL-UHFFFAOYSA-N 0.000 description 2
- HRUSLLQFLRDJRM-UHFFFAOYSA-N n-tert-butyl-3-chloro-n'-(4-chlorobenzoyl)-n'-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1 HRUSLLQFLRDJRM-UHFFFAOYSA-N 0.000 description 2
- LQSNLVISMKPILQ-UHFFFAOYSA-N n-tert-butyl-3-chloro-n'-(4-chlorobenzoyl)-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1 LQSNLVISMKPILQ-UHFFFAOYSA-N 0.000 description 2
- 229910017604 nitric acid Inorganic materials 0.000 description 2
- 231100001160 nonlethal Toxicity 0.000 description 2
- JPMIIZHYYWMHDT-UHFFFAOYSA-N octhilinone Chemical compound CCCCCCCCN1SC=CC1=O JPMIIZHYYWMHDT-UHFFFAOYSA-N 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 2
- 229910052625 palygorskite Inorganic materials 0.000 description 2
- 239000008188 pellet Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 125000003884 phenylalkyl group Chemical group 0.000 description 2
- 229920000151 polyglycol Polymers 0.000 description 2
- 239000010695 polyglycol Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- KJAQRHMKLVGSCG-UHFFFAOYSA-N propan-2-ylhydrazine Chemical compound CC(C)NN KJAQRHMKLVGSCG-UHFFFAOYSA-N 0.000 description 2
- 239000008262 pumice Substances 0.000 description 2
- 239000011435 rock Substances 0.000 description 2
- 239000000741 silica gel Substances 0.000 description 2
- 229910002027 silica gel Inorganic materials 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000012279 sodium borohydride Substances 0.000 description 2
- 229910000033 sodium borohydride Inorganic materials 0.000 description 2
- BEOOHQFXGBMRKU-UHFFFAOYSA-N sodium cyanoborohydride Chemical compound [Na+].[B-]C#N BEOOHQFXGBMRKU-UHFFFAOYSA-N 0.000 description 2
- 241000894007 species Species 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- 150000003512 tertiary amines Chemical class 0.000 description 2
- 150000003606 tin compounds Chemical class 0.000 description 2
- 231100000419 toxicity Toxicity 0.000 description 2
- 230000001988 toxicity Effects 0.000 description 2
- 238000011282 treatment Methods 0.000 description 2
- 239000000080 wetting agent Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 229910052725 zinc Inorganic materials 0.000 description 2
- 239000011701 zinc Substances 0.000 description 2
- ZCVAOQKBXKSDMS-AQYZNVCMSA-N (+)-trans-allethrin Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OC1C(C)=C(CC=C)C(=O)C1 ZCVAOQKBXKSDMS-AQYZNVCMSA-N 0.000 description 1
- CJAAPVQEZPAQNI-UHFFFAOYSA-N (2-methylphenyl)methanamine Chemical compound CC1=CC=CC=C1CN CJAAPVQEZPAQNI-UHFFFAOYSA-N 0.000 description 1
- 125000006526 (C1-C2) alkyl group Chemical group 0.000 description 1
- 125000006536 (C1-C2)alkoxy group Chemical group 0.000 description 1
- 125000003837 (C1-C20) alkyl group Chemical group 0.000 description 1
- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 description 1
- 125000006771 (C1-C6) haloalkylthio group Chemical group 0.000 description 1
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- 125000006528 (C2-C6) alkyl group Chemical group 0.000 description 1
- RHUYHJGZWVXEHW-UHFFFAOYSA-N 1,1-Dimethyhydrazine Chemical compound CN(C)N RHUYHJGZWVXEHW-UHFFFAOYSA-N 0.000 description 1
- JCIIKRHCWVHVFF-UHFFFAOYSA-N 1,2,4-thiadiazol-5-amine;hydrochloride Chemical compound Cl.NC1=NC=NS1 JCIIKRHCWVHVFF-UHFFFAOYSA-N 0.000 description 1
- CFQIQDIUBDMOBX-UHFFFAOYSA-N 1,2-dicyclohexylhydrazine Chemical compound C1CCCCC1NNC1CCCCC1 CFQIQDIUBDMOBX-UHFFFAOYSA-N 0.000 description 1
- BOOQVRGRSDTZRZ-UHFFFAOYSA-N 1,2-dipropylhydrazine Chemical compound CCCNNCCC BOOQVRGRSDTZRZ-UHFFFAOYSA-N 0.000 description 1
- 125000000196 1,4-pentadienyl group Chemical group [H]C([*])=C([H])C([H])([H])C([H])=C([H])[H] 0.000 description 1
- UFIRCPNGJKRFHZ-UHFFFAOYSA-N 1-[(1,6-dimethylcyclohexa-2,4-dien-1-yl)methylamino]-3-phenylurea Chemical compound CC1(C(C=CC=C1)C)CNNC(=O)NC1=CC=CC=C1 UFIRCPNGJKRFHZ-UHFFFAOYSA-N 0.000 description 1
- 125000006083 1-bromoethyl group Chemical group 0.000 description 1
- MJEPOVIWHVRBIT-UHFFFAOYSA-N 1-chloro-4-(4-chlorophenyl)sulfanylbenzene Chemical compound C1=CC(Cl)=CC=C1SC1=CC=C(Cl)C=C1 MJEPOVIWHVRBIT-UHFFFAOYSA-N 0.000 description 1
- BMVXCPBXGZKUPN-UHFFFAOYSA-N 1-hexanamine Chemical compound CCCCCCN BMVXCPBXGZKUPN-UHFFFAOYSA-N 0.000 description 1
- FMTFEIJHMMQUJI-NJAFHUGGSA-N 102130-98-3 Natural products CC=CCC1=C(C)[C@H](CC1=O)OC(=O)[C@@H]1[C@@H](C=C(C)C)C1(C)C FMTFEIJHMMQUJI-NJAFHUGGSA-N 0.000 description 1
- ADMTUGZFHLWYAU-UHFFFAOYSA-N 2,2-dimethylpropylhydrazine Chemical compound CC(C)(C)CNN ADMTUGZFHLWYAU-UHFFFAOYSA-N 0.000 description 1
- SWAXMWAYJKVBNK-UHFFFAOYSA-N 2,3-dimethylbenzenecarbodithioic acid Chemical compound CC1=CC=CC(C(S)=S)=C1C SWAXMWAYJKVBNK-UHFFFAOYSA-N 0.000 description 1
- MHKBMNACOMRIAW-UHFFFAOYSA-N 2,3-dinitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1[N+]([O-])=O MHKBMNACOMRIAW-UHFFFAOYSA-N 0.000 description 1
- QIJIUJYANDSEKG-UHFFFAOYSA-N 2,4,4-trimethylpentan-2-amine Chemical compound CC(C)(C)CC(C)(C)N QIJIUJYANDSEKG-UHFFFAOYSA-N 0.000 description 1
- KRAUIMFQUQXXHC-UHFFFAOYSA-N 2,4-dimethylbenzenecarbodithioic acid Chemical compound CC1=CC=C(C(S)=S)C(C)=C1 KRAUIMFQUQXXHC-UHFFFAOYSA-N 0.000 description 1
- DONBFTMSGYSMNA-UHFFFAOYSA-N 2,6-dichloro-n-ethyl-n'-propan-2-yl-n'-[4-(trifluoromethoxy)benzoyl]benzohydrazide Chemical compound ClC=1C=CC=C(Cl)C=1C(=O)N(CC)N(C(C)C)C(=O)C1=CC=C(OC(F)(F)F)C=C1 DONBFTMSGYSMNA-UHFFFAOYSA-N 0.000 description 1
- RTPVODIBSSFZBK-UHFFFAOYSA-N 2,6-dichloro-n-methyl-n'-propan-2-yl-n'-[4-(trifluoromethoxy)benzoyl]benzohydrazide Chemical compound C=1C=C(OC(F)(F)F)C=CC=1C(=O)N(C(C)C)N(C)C(=O)C1=C(Cl)C=CC=C1Cl RTPVODIBSSFZBK-UHFFFAOYSA-N 0.000 description 1
- NZUXRGMXFCTGBV-UHFFFAOYSA-N 2-(1,1,2,2-tetrachloroethylsulfanyl)-3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical compound C1CC=CC2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)C21 NZUXRGMXFCTGBV-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- XBEIANFIOZTEDE-UHFFFAOYSA-N 2-(benzenecarbonothioylsulfanyl)acetic acid Chemical compound OC(=O)CSC(=S)C1=CC=CC=C1 XBEIANFIOZTEDE-UHFFFAOYSA-N 0.000 description 1
- UPTVJAJPBGIRLZ-UHFFFAOYSA-N 2-(trichloromethylsulfanyl)-3a,4,5,7a-tetrahydroisoindole-1,3-dione Chemical compound C1CC=CC2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C21 UPTVJAJPBGIRLZ-UHFFFAOYSA-N 0.000 description 1
- XNWFRZJHXBZDAG-UHFFFAOYSA-N 2-METHOXYETHANOL Chemical compound COCCO XNWFRZJHXBZDAG-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- APWCDRXIKLVLAO-UHFFFAOYSA-N 2-[2-[[tert-butyl-[4-(dimethylcarbamoyloxy)benzoyl]amino]-ethylcarbamoyl]phenyl]acetic acid Chemical compound C=1C=CC=C(CC(O)=O)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(OC(=O)N(C)C)C=C1 APWCDRXIKLVLAO-UHFFFAOYSA-N 0.000 description 1
- HBYYEIZICLSADI-UHFFFAOYSA-N 2-[2-[[tert-butyl-[4-(dimethylcarbamoyloxy)benzoyl]amino]-methylcarbamoyl]phenyl]acetic acid Chemical compound C1=CC(OC(=O)N(C)C)=CC=C1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=CC=C1CC(O)=O HBYYEIZICLSADI-UHFFFAOYSA-N 0.000 description 1
- WUWIZBYGOFAMPN-UHFFFAOYSA-N 2-[tert-butyl-[[4-(chloromethyl)benzoyl]-ethylamino]carbamoyl]benzoic acid Chemical compound C=1C=C(CCl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1C(O)=O WUWIZBYGOFAMPN-UHFFFAOYSA-N 0.000 description 1
- JLJCEQHAOKZCHZ-UHFFFAOYSA-N 2-[tert-butyl-[[4-(chloromethyl)benzoyl]-methylamino]carbamoyl]benzoic acid Chemical compound C=1C=C(CCl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1C(O)=O JLJCEQHAOKZCHZ-UHFFFAOYSA-N 0.000 description 1
- RJFKYQSECBPFPR-UHFFFAOYSA-N 2-benzoylbenzenecarbothiohydrazide Chemical compound NNC(=S)C1=CC=CC=C1C(=O)C1=CC=CC=C1 RJFKYQSECBPFPR-UHFFFAOYSA-N 0.000 description 1
- RRXBOAFUCKTFOJ-UHFFFAOYSA-N 2-benzyl-1,1-dimethylhydrazine Chemical compound CN(C)NCC1=CC=CC=C1 RRXBOAFUCKTFOJ-UHFFFAOYSA-N 0.000 description 1
- NZHBKABQIVFUNQ-UHFFFAOYSA-N 2-bromo-n'-tert-butyl-n'-(4-ethenylbenzoyl)-n-ethylbenzohydrazide Chemical compound C=1C=CC=C(Br)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C=C)C=C1 NZHBKABQIVFUNQ-UHFFFAOYSA-N 0.000 description 1
- GJYIFAVESBCDDX-UHFFFAOYSA-N 2-bromo-n'-tert-butyl-n'-(4-ethenylbenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=CC=C(Br)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C=C)C=C1 GJYIFAVESBCDDX-UHFFFAOYSA-N 0.000 description 1
- OVKUKDFLYRBPML-UHFFFAOYSA-N 2-bromo-n-(2,2-dimethylpropyl)-n'-(4-methylbenzoyl)-n'-prop-2-ynylbenzohydrazide Chemical compound C1=CC(C)=CC=C1C(=O)N(CC#C)N(CC(C)(C)C)C(=O)C1=CC=CC=C1Br OVKUKDFLYRBPML-UHFFFAOYSA-N 0.000 description 1
- DBUPZLCKWFVDBK-UHFFFAOYSA-N 2-bromo-n-tert-butyl-n'-(3-ethoxybenzoyl)-n'-propylbenzohydrazide Chemical compound C=1C=CC(OCC)=CC=1C(=O)N(CCC)N(C(C)(C)C)C(=O)C1=CC=CC=C1Br DBUPZLCKWFVDBK-UHFFFAOYSA-N 0.000 description 1
- SXLQKDBCNFBWPJ-UHFFFAOYSA-N 2-bromo-n-tert-butyl-n'-[4-(2-chloroacetyl)benzoyl]-n'-ethylbenzohydrazide Chemical compound C=1C=C(C(=O)CCl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1Br SXLQKDBCNFBWPJ-UHFFFAOYSA-N 0.000 description 1
- NRDHONGOARDSAD-UHFFFAOYSA-N 2-bromo-n-tert-butyl-n'-[4-(2-chloroacetyl)benzoyl]-n'-methylbenzohydrazide Chemical compound C=1C=C(C(=O)CCl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1Br NRDHONGOARDSAD-UHFFFAOYSA-N 0.000 description 1
- BUWBHDATLDIKGI-UHFFFAOYSA-N 2-bromo-n-tert-butyl-n'-ethyl-n'-(3-phenoxybenzoyl)benzohydrazide Chemical compound C=1C=CC(OC=2C=CC=CC=2)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1Br BUWBHDATLDIKGI-UHFFFAOYSA-N 0.000 description 1
- JABOTSOOJNCALH-UHFFFAOYSA-N 2-bromo-n-tert-butyl-n'-methyl-n'-(3-phenoxybenzoyl)benzohydrazide Chemical compound C=1C=CC(OC=2C=CC=CC=2)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1Br JABOTSOOJNCALH-UHFFFAOYSA-N 0.000 description 1
- NZCKTGCKFJDGFD-UHFFFAOYSA-N 2-bromobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Br NZCKTGCKFJDGFD-UHFFFAOYSA-N 0.000 description 1
- 125000005999 2-bromoethyl group Chemical group 0.000 description 1
- YAUCKEPYKXHCFF-UHFFFAOYSA-N 2-carbamothioylsulfanylethyl carbamodithioate;manganese Chemical compound [Mn].NC(=S)SCCSC(N)=S YAUCKEPYKXHCFF-UHFFFAOYSA-N 0.000 description 1
- MQLHZNDUTVBYFI-UHFFFAOYSA-N 2-chloro-n-(4-ethylbenzoyl)-5-methyl-n'-(trimethylsilyloxymethyl)benzohydrazide Chemical compound C1=CC(CC)=CC=C1C(=O)N(NCO[Si](C)(C)C)C(=O)C1=CC(C)=CC=C1Cl MQLHZNDUTVBYFI-UHFFFAOYSA-N 0.000 description 1
- LTHNHFOGQMKPOV-UHFFFAOYSA-N 2-ethylhexan-1-amine Chemical compound CCCCC(CC)CN LTHNHFOGQMKPOV-UHFFFAOYSA-N 0.000 description 1
- KDOKFXJQGPCGLT-UHFFFAOYSA-N 2-hydroxyethyl-dimethyl-octadecylazanium Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CCO KDOKFXJQGPCGLT-UHFFFAOYSA-N 0.000 description 1
- ASUDFOJKTJLAIK-UHFFFAOYSA-N 2-methoxyethanamine Chemical compound COCCN ASUDFOJKTJLAIK-UHFFFAOYSA-N 0.000 description 1
- KFXLXEQCRFGDRU-UHFFFAOYSA-N 2-methylbenzohydrazide Chemical compound CC1=CC=CC=C1C(=O)NN KFXLXEQCRFGDRU-UHFFFAOYSA-N 0.000 description 1
- NGSOWKPBNFOQCR-UHFFFAOYSA-N 2-methylpropylhydrazine Chemical compound CC(C)CNN NGSOWKPBNFOQCR-UHFFFAOYSA-N 0.000 description 1
- BRKAFSPFDZRZSD-UHFFFAOYSA-N 3,4-dichloro-n'-(4-methylbenzenecarbothioyl)-n-propan-2-yl-n'-propylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=S)N(CCC)N(C(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 BRKAFSPFDZRZSD-UHFFFAOYSA-N 0.000 description 1
- DNISXKBKTSHNKL-UHFFFAOYSA-N 3,5-dichlorobenzohydrazide Chemical compound NNC(=O)C1=CC(Cl)=CC(Cl)=C1 DNISXKBKTSHNKL-UHFFFAOYSA-N 0.000 description 1
- GGHLXLVPNZMBQR-UHFFFAOYSA-N 3,5-dichlorobenzoyl chloride Chemical compound ClC(=O)C1=CC(Cl)=CC(Cl)=C1 GGHLXLVPNZMBQR-UHFFFAOYSA-N 0.000 description 1
- QGFBIGCZVGELMV-UHFFFAOYSA-N 3-(bromomethyl)-n-methyl-n'-(2-methylpropyl)-n'-(4-propan-2-yloxybenzoyl)benzohydrazide Chemical compound C=1C=C(OC(C)C)C=CC=1C(=O)N(CC(C)C)N(C)C(=O)C1=CC=CC(CBr)=C1 QGFBIGCZVGELMV-UHFFFAOYSA-N 0.000 description 1
- DFDGEUZMOJMFQY-UHFFFAOYSA-N 3-(hydroxyamino)-n-methyl-n'-propan-2-yl-n'-[4-(tribromomethyl)benzoyl]benzohydrazide Chemical compound C=1C=C(C(Br)(Br)Br)C=CC=1C(=O)N(C(C)C)N(C)C(=O)C1=CC=CC(NO)=C1 DFDGEUZMOJMFQY-UHFFFAOYSA-N 0.000 description 1
- BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 1
- CNXCMTRKIZUIFU-UHFFFAOYSA-N 3-bromo-4-methoxy-n-methyl-n'-propan-2-yl-n'-(4-sulfanylbenzoyl)benzohydrazide Chemical compound C1=C(Br)C(OC)=CC=C1C(=O)N(C)N(C(C)C)C(=O)C1=CC=C(S)C=C1 CNXCMTRKIZUIFU-UHFFFAOYSA-N 0.000 description 1
- JBMPSCAQNPYSFQ-UHFFFAOYSA-N 3-bromo-n'-butan-2-yl-2-(chloromethyl)-n'-[3-(cyanomethyl)benzoyl]-4-fluoro-n-methylbenzohydrazide Chemical compound C=1C=CC(CC#N)=CC=1C(=O)N(C(C)CC)N(C)C(=O)C1=CC=C(F)C(Br)=C1CCl JBMPSCAQNPYSFQ-UHFFFAOYSA-N 0.000 description 1
- UJSGJGBKFYLISG-UHFFFAOYSA-N 3-bromo-n-ethyl-4-methoxy-n'-propan-2-yl-n'-(4-sulfanylbenzoyl)benzohydrazide Chemical compound C=1C=C(OC)C(Br)=CC=1C(=O)N(CC)N(C(C)C)C(=O)C1=CC=C(S)C=C1 UJSGJGBKFYLISG-UHFFFAOYSA-N 0.000 description 1
- RPESZQVUWMFBEO-UHFFFAOYSA-N 3-cyanobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC(C#N)=C1 RPESZQVUWMFBEO-UHFFFAOYSA-N 0.000 description 1
- LVJAZWNACGZVRQ-UHFFFAOYSA-N 3-methylbutylhydrazine Chemical compound CC(C)CCNN LVJAZWNACGZVRQ-UHFFFAOYSA-N 0.000 description 1
- ZXVONLUNISGICL-UHFFFAOYSA-N 4,6-dinitro-o-cresol Chemical compound CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O ZXVONLUNISGICL-UHFFFAOYSA-N 0.000 description 1
- ACVLVBVKIBVNDT-UHFFFAOYSA-N 4-(chloromethyl)benzenecarbodithioic acid Chemical compound SC(=S)C1=CC=C(CCl)C=C1 ACVLVBVKIBVNDT-UHFFFAOYSA-N 0.000 description 1
- CDIJOYCNNFLOAX-UHFFFAOYSA-N 4-(trichloromethylsulfanyl)isoindole-1,3-dione Chemical compound ClC(Cl)(Cl)SC1=CC=CC2=C1C(=O)NC2=O CDIJOYCNNFLOAX-UHFFFAOYSA-N 0.000 description 1
- PHZPOPLZHWSIDP-UHFFFAOYSA-N 4-[[butan-2-yl-(3,4,5-trichlorobenzoyl)amino]-ethylcarbamoyl]benzoic acid Chemical compound C=1C(Cl)=C(Cl)C(Cl)=CC=1C(=O)N(C(C)CC)N(CC)C(=O)C1=CC=C(C(O)=O)C=C1 PHZPOPLZHWSIDP-UHFFFAOYSA-N 0.000 description 1
- SJOPPXZFFUKMAF-UHFFFAOYSA-N 4-[[butan-2-yl-(3,4,5-trichlorobenzoyl)amino]-methylcarbamoyl]benzoic acid Chemical compound C=1C(Cl)=C(Cl)C(Cl)=CC=1C(=O)N(C(C)CC)N(C)C(=O)C1=CC=C(C(O)=O)C=C1 SJOPPXZFFUKMAF-UHFFFAOYSA-N 0.000 description 1
- YMFAALOKWQNULN-UHFFFAOYSA-N 4-[butan-2-yl-[(2-carbamoylbenzoyl)-ethylamino]carbamoyl]-3-chloro-n-ethylbenzamide Chemical compound ClC1=CC(C(=O)NCC)=CC=C1C(=O)N(C(C)CC)N(CC)C(=O)C1=CC=CC=C1C(N)=O YMFAALOKWQNULN-UHFFFAOYSA-N 0.000 description 1
- ZAQOSCAAQIZCOB-UHFFFAOYSA-N 4-[butan-2-yl-[(2-carbamoylbenzoyl)-methylamino]carbamoyl]-3-chloro-n-ethylbenzamide Chemical compound ClC1=CC(C(=O)NCC)=CC=C1C(=O)N(C(C)CC)N(C)C(=O)C1=CC=CC=C1C(N)=O ZAQOSCAAQIZCOB-UHFFFAOYSA-N 0.000 description 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 description 1
- PKBGHORNUFQAAW-UHFFFAOYSA-N 4-chlorobenzohydrazide Chemical compound NNC(=O)C1=CC=C(Cl)C=C1 PKBGHORNUFQAAW-UHFFFAOYSA-N 0.000 description 1
- RKIDDEGICSMIJA-UHFFFAOYSA-N 4-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=C(Cl)C=C1 RKIDDEGICSMIJA-UHFFFAOYSA-N 0.000 description 1
- 125000006283 4-chlorobenzyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1Cl)C([H])([H])* 0.000 description 1
- MFFVZXOPRXMVET-UHFFFAOYSA-N 4-methylbenzohydrazide Chemical compound CC1=CC=C(C(=O)NN)C=C1 MFFVZXOPRXMVET-UHFFFAOYSA-N 0.000 description 1
- NQUVCRCCRXRJCK-UHFFFAOYSA-N 4-methylbenzoyl chloride Chemical compound CC1=CC=C(C(Cl)=O)C=C1 NQUVCRCCRXRJCK-UHFFFAOYSA-N 0.000 description 1
- 125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 description 1
- ODVBBZFQPGORMJ-UHFFFAOYSA-N 4-nitrobenzylamine Chemical compound NCC1=CC=C([N+]([O-])=O)C=C1 ODVBBZFQPGORMJ-UHFFFAOYSA-N 0.000 description 1
- 125000002373 5 membered heterocyclic group Chemical group 0.000 description 1
- JFCNFKFFTWFMLR-UHFFFAOYSA-N 5-[ethyl-[propan-2-yl-[4-(trifluoromethyl)benzoyl]amino]carbamoyl]-n,n,2-trimethylbenzamide Chemical compound C=1C=C(C)C(C(=O)N(C)C)=CC=1C(=O)N(CC)N(C(C)C)C(=O)C1=CC=C(C(F)(F)F)C=C1 JFCNFKFFTWFMLR-UHFFFAOYSA-N 0.000 description 1
- 125000004070 6 membered heterocyclic group Chemical group 0.000 description 1
- AQECUUPLGRRRTJ-UHFFFAOYSA-N 6-methylheptylhydrazine Chemical compound CC(C)CCCCCNN AQECUUPLGRRRTJ-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- 244000215068 Acacia senegal Species 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 108010088751 Albumins Proteins 0.000 description 1
- 102000009027 Albumins Human genes 0.000 description 1
- RGCKGOZRHPZPFP-UHFFFAOYSA-N Alizarin Natural products C1=CC=C2C(=O)C3=C(O)C(O)=CC=C3C(=O)C2=C1 RGCKGOZRHPZPFP-UHFFFAOYSA-N 0.000 description 1
- 241000193388 Bacillus thuringiensis Species 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- 235000018185 Betula X alpestris Nutrition 0.000 description 1
- 235000018212 Betula X uliginosa Nutrition 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- FIPWRIJSWJWJAI-UHFFFAOYSA-N Butyl carbitol 6-propylpiperonyl ether Chemical compound C1=C(CCC)C(COCCOCCOCCCC)=CC2=C1OCO2 FIPWRIJSWJWJAI-UHFFFAOYSA-N 0.000 description 1
- DHPRFNDAJCKMAL-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)N(NC(C)C)C(C1=CC=CC=C1)=O Chemical compound C(C1=CC=CC=C1)(=O)N(NC(C)C)C(C1=CC=CC=C1)=O DHPRFNDAJCKMAL-UHFFFAOYSA-N 0.000 description 1
- VILXUAVBRXFNFJ-UHFFFAOYSA-N C=1C=CC(CC#N)=CC=1C(=O)N(C(C)CC)N(CC)C(=O)C1=CC=C(F)C(Br)=C1CCl Chemical compound C=1C=CC(CC#N)=CC=1C(=O)N(C(C)CC)N(CC)C(=O)C1=CC=C(F)C(Br)=C1CCl VILXUAVBRXFNFJ-UHFFFAOYSA-N 0.000 description 1
- JOIQIUVYCDOANM-UHFFFAOYSA-N CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1C(=C(C)C)C(O)=O Chemical compound CCC(C)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1C(=C(C)C)C(O)=O JOIQIUVYCDOANM-UHFFFAOYSA-N 0.000 description 1
- 229910021532 Calcite Inorganic materials 0.000 description 1
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- 229920002134 Carboxymethyl cellulose Polymers 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- XJUZRXYOEPSWMB-UHFFFAOYSA-N Chloromethyl methyl ether Chemical compound COCCl XJUZRXYOEPSWMB-UHFFFAOYSA-N 0.000 description 1
- 241000207199 Citrus Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- VMQMZMRVKUZKQL-UHFFFAOYSA-N Cu+ Chemical compound [Cu+] VMQMZMRVKUZKQL-UHFFFAOYSA-N 0.000 description 1
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- 241001635274 Cydia pomonella Species 0.000 description 1
- ZAKOWWREFLAJOT-CEFNRUSXSA-N D-alpha-tocopherylacetate Chemical compound CC(=O)OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C ZAKOWWREFLAJOT-CEFNRUSXSA-N 0.000 description 1
- YVGGHNCTFXOJCH-UHFFFAOYSA-N DDT Chemical compound C1=CC(Cl)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(Cl)C=C1 YVGGHNCTFXOJCH-UHFFFAOYSA-N 0.000 description 1
- 239000004338 Dichlorodifluoromethane Substances 0.000 description 1
- 241000462639 Epilachna varivestis Species 0.000 description 1
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical class CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 1
- CWYNVVGOOAEACU-UHFFFAOYSA-N Fe2+ Chemical compound [Fe+2] CWYNVVGOOAEACU-UHFFFAOYSA-N 0.000 description 1
- VTLYFUHAOXGGBS-UHFFFAOYSA-N Fe3+ Chemical compound [Fe+3] VTLYFUHAOXGGBS-UHFFFAOYSA-N 0.000 description 1
- SPJOZZSIXXJYBT-UHFFFAOYSA-N Fenson Chemical compound C1=CC(Cl)=CC=C1OS(=O)(=O)C1=CC=CC=C1 SPJOZZSIXXJYBT-UHFFFAOYSA-N 0.000 description 1
- 239000004606 Fillers/Extenders Substances 0.000 description 1
- 241000233866 Fungi Species 0.000 description 1
- 206010053759 Growth retardation Diseases 0.000 description 1
- 229920000084 Gum arabic Polymers 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 206010061217 Infestation Diseases 0.000 description 1
- 240000007049 Juglans regia Species 0.000 description 1
- 235000009496 Juglans regia Nutrition 0.000 description 1
- 229920001732 Lignosulfonate Polymers 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- ZOKXTWBITQBERF-UHFFFAOYSA-N Molybdenum Chemical compound [Mo] ZOKXTWBITQBERF-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 244000100170 Phaseolus lunatus Species 0.000 description 1
- 235000010617 Phaseolus lunatus Nutrition 0.000 description 1
- 244000046052 Phaseolus vulgaris Species 0.000 description 1
- 235000010627 Phaseolus vulgaris Nutrition 0.000 description 1
- BHHGXPLMPWCGHP-UHFFFAOYSA-N Phenethylamine Chemical compound NCCC1=CC=CC=C1 BHHGXPLMPWCGHP-UHFFFAOYSA-N 0.000 description 1
- 241000218657 Picea Species 0.000 description 1
- 235000008331 Pinus X rigitaeda Nutrition 0.000 description 1
- 241000018646 Pinus brutia Species 0.000 description 1
- 235000011613 Pinus brutia Nutrition 0.000 description 1
- NQRYJNQNLNOLGT-UHFFFAOYSA-O Piperidinium(1+) Chemical compound C1CC[NH2+]CC1 NQRYJNQNLNOLGT-UHFFFAOYSA-O 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- WTKZEGDFNFYCGP-UHFFFAOYSA-O Pyrazolium Chemical compound C1=CN[NH+]=C1 WTKZEGDFNFYCGP-UHFFFAOYSA-O 0.000 description 1
- 235000003694 Randia formosa Nutrition 0.000 description 1
- 244000039072 Randia formosa Species 0.000 description 1
- 239000004113 Sepiolite Substances 0.000 description 1
- UIIMBOGNXHQVGW-DEQYMQKBSA-M Sodium bicarbonate-14C Chemical compound [Na+].O[14C]([O-])=O UIIMBOGNXHQVGW-DEQYMQKBSA-M 0.000 description 1
- BCKXLBQYZLBQEK-KVVVOXFISA-M Sodium oleate Chemical compound [Na+].CCCCCCCC\C=C/CCCCCCCC([O-])=O BCKXLBQYZLBQEK-KVVVOXFISA-M 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical compound OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- QUWSDLYBOVGOCW-UHFFFAOYSA-N Tetrasul Chemical compound C1=CC(Cl)=CC=C1SC1=CC(Cl)=C(Cl)C=C1Cl QUWSDLYBOVGOCW-UHFFFAOYSA-N 0.000 description 1
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- BABJTMNVJXLAEX-UHFFFAOYSA-N Triamiphos Chemical compound N1=C(N)N(P(=O)(N(C)C)N(C)C)N=C1C1=CC=CC=C1 BABJTMNVJXLAEX-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 229920004894 Triton X-305 Polymers 0.000 description 1
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical group ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 1
- BLIOPNNXQBRCMJ-UHFFFAOYSA-N [2-[[benzoyl(ethyl)amino]-tert-butylcarbamoyl]phenyl] acetate Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1OC(C)=O BLIOPNNXQBRCMJ-UHFFFAOYSA-N 0.000 description 1
- ZUQOBIPRJHGFDH-UHFFFAOYSA-N [2-[[benzoyl(methyl)amino]-tert-butylcarbamoyl]phenyl] acetate Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1OC(C)=O ZUQOBIPRJHGFDH-UHFFFAOYSA-N 0.000 description 1
- PEJJZCRBCYMACJ-UHFFFAOYSA-N [3-[3,3-dimethylbutan-2-yl-[ethyl-(4-propylbenzoyl)amino]carbamoyl]phenyl] ethyl carbonate Chemical compound C1=CC(CCC)=CC=C1C(=O)N(CC)N(C(C)C(C)(C)C)C(=O)C1=CC=CC(OC(=O)OCC)=C1 PEJJZCRBCYMACJ-UHFFFAOYSA-N 0.000 description 1
- CZXMCJNNBQZPGI-UHFFFAOYSA-N [3-[3,3-dimethylbutan-2-yl-[methyl-(4-propylbenzoyl)amino]carbamoyl]phenyl] ethyl carbonate Chemical compound C1=CC(CCC)=CC=C1C(=O)N(C)N(C(C)C(C)(C)C)C(=O)C1=CC=CC(OC(=O)OCC)=C1 CZXMCJNNBQZPGI-UHFFFAOYSA-N 0.000 description 1
- BYZYEQOUKRAOCW-UHFFFAOYSA-N [3-[[(2,5-dibromobenzoyl)-propan-2-ylamino]-ethylcarbamoyl]phenyl] propanoate Chemical compound C=1C=CC(OC(=O)CC)=CC=1C(=O)N(CC)N(C(C)C)C(=O)C1=CC(Br)=CC=C1Br BYZYEQOUKRAOCW-UHFFFAOYSA-N 0.000 description 1
- YDLQWPZUHITOIT-UHFFFAOYSA-N [3-[[(2,5-dibromobenzoyl)-propan-2-ylamino]-methylcarbamoyl]phenyl] propanoate Chemical compound CCC(=O)OC1=CC=CC(C(=O)N(C)N(C(C)C)C(=O)C=2C(=CC=C(Br)C=2)Br)=C1 YDLQWPZUHITOIT-UHFFFAOYSA-N 0.000 description 1
- HYYSAOWFXKIBEZ-UHFFFAOYSA-N [3-[[tert-butyl-[2-chloro-4-(trichloromethyl)benzenecarbothioyl]amino]-ethylcarbamoyl]phenyl] trifluoromethanesulfonate Chemical compound C=1C=CC(OS(=O)(=O)C(F)(F)F)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=S)C1=CC=C(C(Cl)(Cl)Cl)C=C1Cl HYYSAOWFXKIBEZ-UHFFFAOYSA-N 0.000 description 1
- GDZCVVUUBBVTLP-UHFFFAOYSA-N [3-[[tert-butyl-[2-chloro-4-(trichloromethyl)benzenecarbothioyl]amino]-methylcarbamoyl]phenyl] trifluoromethanesulfonate Chemical compound C=1C=CC(OS(=O)(=O)C(F)(F)F)=CC=1C(=O)N(C)N(C(C)(C)C)C(=S)C1=CC=C(C(Cl)(Cl)Cl)C=C1Cl GDZCVVUUBBVTLP-UHFFFAOYSA-N 0.000 description 1
- HAGGMUGXQVIQAL-UHFFFAOYSA-N [4,4-dichloro-1-(trichloromethyl)cyclohexa-2,5-dien-1-yl]-phenylmethanol Chemical compound C1=CC(Cl)(Cl)C=CC1(C(Cl)(Cl)Cl)C(O)C1=CC=CC=C1 HAGGMUGXQVIQAL-UHFFFAOYSA-N 0.000 description 1
- OCWVPTAURXQRBK-UHFFFAOYSA-N [4-[[(2-bromobenzoyl)-(3,3-dimethylbutan-2-yl)amino]-ethylcarbamoyl]phenyl]urea Chemical compound C=1C=C(NC(N)=O)C=CC=1C(=O)N(CC)N(C(C)C(C)(C)C)C(=O)C1=CC=CC=C1Br OCWVPTAURXQRBK-UHFFFAOYSA-N 0.000 description 1
- HPQKQCUBERRGEQ-UHFFFAOYSA-N [4-[[(2-bromobenzoyl)-(3,3-dimethylbutan-2-yl)amino]-methylcarbamoyl]phenyl]urea Chemical compound C=1C=CC=C(Br)C=1C(=O)N(C(C)C(C)(C)C)N(C)C(=O)C1=CC=C(NC(N)=O)C=C1 HPQKQCUBERRGEQ-UHFFFAOYSA-N 0.000 description 1
- LPEHHEMKMJANMT-UHFFFAOYSA-N [4-[[benzoyl(ethyl)amino]-tert-butylcarbamoyl]phenyl] methanesulfonate Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(OS(C)(=O)=O)C=C1 LPEHHEMKMJANMT-UHFFFAOYSA-N 0.000 description 1
- AYXJUTPDMURGMZ-UHFFFAOYSA-N [4-[[benzoyl(methyl)amino]-tert-butylcarbamoyl]phenyl] methanesulfonate Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(OS(C)(=O)=O)C=C1 AYXJUTPDMURGMZ-UHFFFAOYSA-N 0.000 description 1
- ZTQWMQUOVKFHQL-UHFFFAOYSA-N [4-[tert-butyl-[(2-chlorobenzoyl)-ethylamino]carbamoyl]phenyl] thiohypochlorite Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(SCl)C=C1 ZTQWMQUOVKFHQL-UHFFFAOYSA-N 0.000 description 1
- QRHPUMMMNMKSEJ-UHFFFAOYSA-N [4-[tert-butyl-[(2-chlorobenzoyl)-methylamino]carbamoyl]phenyl] thiohypochlorite Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(SCl)C=C1 QRHPUMMMNMKSEJ-UHFFFAOYSA-N 0.000 description 1
- PBPSDDICYUODSU-UHFFFAOYSA-N [4-[tert-butyl-[(3,5-dimethylbenzoyl)-methylamino]carbamoyl]phenyl] 2,2-dimethylpropanoate Chemical compound C=1C(C)=CC(C)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(OC(=O)C(C)(C)C)C=C1 PBPSDDICYUODSU-UHFFFAOYSA-N 0.000 description 1
- YIVGFGJDPJJMDT-UHFFFAOYSA-N [6-benzoyl-6-(hydrazinylmethyl)cyclohexa-2,4-dien-1-yl]-phenylmethanone Chemical compound C=1C=CC=CC=1C(=O)C1(CNN)C=CC=CC1C(=O)C1=CC=CC=C1 YIVGFGJDPJJMDT-UHFFFAOYSA-N 0.000 description 1
- 239000000205 acacia gum Substances 0.000 description 1
- 235000010489 acacia gum Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
- HFVAFDPGUJEFBQ-UHFFFAOYSA-M alizarin red S Chemical compound [Na+].O=C1C2=CC=CC=C2C(=O)C2=C1C=C(S([O-])(=O)=O)C(O)=C2O HFVAFDPGUJEFBQ-UHFFFAOYSA-M 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 229940045714 alkyl sulfonate alkylating agent Drugs 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229940024113 allethrin Drugs 0.000 description 1
- HFEHLDPGIKPNKL-UHFFFAOYSA-N allyl iodide Chemical compound ICC=C HFEHLDPGIKPNKL-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- 150000001409 amidines Chemical class 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 125000005228 aryl sulfonate group Chemical group 0.000 description 1
- 239000000987 azo dye Substances 0.000 description 1
- 229940097012 bacillus thuringiensis Drugs 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- DSAJWYNOEDNPEQ-UHFFFAOYSA-N barium atom Chemical compound [Ba] DSAJWYNOEDNPEQ-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- WARCRYXKINZHGQ-UHFFFAOYSA-N benzohydrazide Chemical compound NNC(=O)C1=CC=CC=C1 WARCRYXKINZHGQ-UHFFFAOYSA-N 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- MQNMFRWOJNAANI-UHFFFAOYSA-N benzyl 2-[[(4-bromo-2-methoxybenzoyl)-tert-butylamino]-ethylcarbamoyl]benzoate Chemical compound C=1C=CC=C(C(=O)OCC=2C=CC=CC=2)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Br)C=C1OC MQNMFRWOJNAANI-UHFFFAOYSA-N 0.000 description 1
- NHGLCYJYMKDECT-UHFFFAOYSA-N benzyl 2-[[(4-bromo-2-methoxybenzoyl)-tert-butylamino]-methylcarbamoyl]benzoate Chemical compound COC1=CC(Br)=CC=C1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=CC=C1C(=O)OCC1=CC=CC=C1 NHGLCYJYMKDECT-UHFFFAOYSA-N 0.000 description 1
- AGEZXYOZHKGVCM-UHFFFAOYSA-N benzyl bromide Chemical compound BrCC1=CC=CC=C1 AGEZXYOZHKGVCM-UHFFFAOYSA-N 0.000 description 1
- YOUGRGFIHBUKRS-UHFFFAOYSA-N benzyl(trimethyl)azanium Chemical compound C[N+](C)(C)CC1=CC=CC=C1 YOUGRGFIHBUKRS-UHFFFAOYSA-N 0.000 description 1
- VEMKTZHHVJILDY-UXHICEINSA-N bioresmethrin Chemical compound 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 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-O bis(2-hydroxyethyl)azanium Chemical compound OCC[NH2+]CCO ZBCBWPMODOFKDW-UHFFFAOYSA-O 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 244000309464 bull Species 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical compound [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 description 1
- 235000013539 calcium stearate Nutrition 0.000 description 1
- 239000008116 calcium stearate Substances 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- CVXBEEMKQHEXEN-UHFFFAOYSA-N carbaryl Chemical compound C1=CC=C2C(OC(=O)NC)=CC=CC2=C1 CVXBEEMKQHEXEN-UHFFFAOYSA-N 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- WBKIJSTULNTGSD-UHFFFAOYSA-N carbonodithioic s,s-acid;2-methylquinoxaline Chemical compound OC(S)=S.C1=CC=CC2=NC(C)=CN=C21 WBKIJSTULNTGSD-UHFFFAOYSA-N 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- 235000010948 carboxy methyl cellulose Nutrition 0.000 description 1
- 239000008112 carboxymethyl-cellulose Substances 0.000 description 1
- 239000005018 casein Substances 0.000 description 1
- BECPQYXYKAMYBN-UHFFFAOYSA-N casein, tech. Chemical compound NCCCCC(C(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(CC(C)C)N=C(O)C(CCC(O)=O)N=C(O)C(CC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(C(C)O)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=N)N=C(O)C(CCC(O)=O)N=C(O)C(CCC(O)=O)N=C(O)C(COP(O)(O)=O)N=C(O)C(CCC(O)=N)N=C(O)C(N)CC1=CC=CC=C1 BECPQYXYKAMYBN-UHFFFAOYSA-N 0.000 description 1
- 235000021240 caseins Nutrition 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- STUSTWKEFDQFFZ-KPKJPENVSA-N chlordimeform Chemical compound CN(C)\C=N\C1=CC=C(Cl)C=C1C STUSTWKEFDQFFZ-KPKJPENVSA-N 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- JWMLCCRPDOIBAV-UHFFFAOYSA-N chloro(methylsulfanyl)methane Chemical compound CSCCl JWMLCCRPDOIBAV-UHFFFAOYSA-N 0.000 description 1
- 150000008422 chlorobenzenes Chemical class 0.000 description 1
- 125000004218 chloromethyl group Chemical group [H]C([H])(Cl)* 0.000 description 1
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 description 1
- AFYPFACVUDMOHA-UHFFFAOYSA-N chlorotrifluoromethane Chemical compound FC(F)(F)Cl AFYPFACVUDMOHA-UHFFFAOYSA-N 0.000 description 1
- 235000020971 citrus fruits Nutrition 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 239000010941 cobalt Substances 0.000 description 1
- 229910017052 cobalt Inorganic materials 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 229910052681 coesite Inorganic materials 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000007859 condensation product Substances 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 229910052906 cristobalite Inorganic materials 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 230000001955 cumulated effect Effects 0.000 description 1
- 150000001924 cycloalkanes Chemical class 0.000 description 1
- WCMMILVIRZAPLE-UHFFFAOYSA-M cyhexatin Chemical compound C1CCCCC1[Sn](C1CCCCC1)(O)C1CCCCC1 WCMMILVIRZAPLE-UHFFFAOYSA-M 0.000 description 1
- RKMJXTWHATWGNX-UHFFFAOYSA-N decyltrimethylammonium ion Chemical compound CCCCCCCCCC[N+](C)(C)C RKMJXTWHATWGNX-UHFFFAOYSA-N 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 125000005131 dialkylammonium group Chemical group 0.000 description 1
- GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- XBPCUCUWBYBCDP-UHFFFAOYSA-O dicyclohexylazanium Chemical compound C1CCCCC1[NH2+]C1CCCCC1 XBPCUCUWBYBCDP-UHFFFAOYSA-O 0.000 description 1
- 238000004512 die casting Methods 0.000 description 1
- RRBNGQHBEYUPFC-UHFFFAOYSA-N diethyl-(2-hydroxyethyl)-octylazanium Chemical compound CCCCCCCC[N+](CC)(CC)CCO RRBNGQHBEYUPFC-UHFFFAOYSA-N 0.000 description 1
- UAOMVDZJSHZZME-UHFFFAOYSA-N diisopropylamine Chemical compound CC(C)NC(C)C UAOMVDZJSHZZME-UHFFFAOYSA-N 0.000 description 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- LTYMSROWYAPPGB-UHFFFAOYSA-N diphenyl sulfide Chemical class C=1C=CC=CC=1SC1=CC=CC=C1 LTYMSROWYAPPGB-UHFFFAOYSA-N 0.000 description 1
- 238000000921 elemental analysis Methods 0.000 description 1
- 238000004945 emulsification Methods 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000008029 eradication Effects 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- WDQNIWFZKXZFAY-UHFFFAOYSA-M fentin acetate Chemical compound CC([O-])=O.C1=CC=CC=C1[Sn+](C=1C=CC=CC=1)C1=CC=CC=C1 WDQNIWFZKXZFAY-UHFFFAOYSA-M 0.000 description 1
- BFWMWWXRWVJXSE-UHFFFAOYSA-M fentin hydroxide Chemical compound C=1C=CC=CC=1[Sn](C=1C=CC=CC=1)(O)C1=CC=CC=C1 BFWMWWXRWVJXSE-UHFFFAOYSA-M 0.000 description 1
- 239000003337 fertilizer Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 230000037406 food intake Effects 0.000 description 1
- 239000000446 fuel Substances 0.000 description 1
- 230000000855 fungicidal effect Effects 0.000 description 1
- 235000021552 granulated sugar Nutrition 0.000 description 1
- 239000001963 growth medium Substances 0.000 description 1
- 231100000001 growth retardation Toxicity 0.000 description 1
- 239000003630 growth substance Substances 0.000 description 1
- 239000010440 gypsum Substances 0.000 description 1
- 229910052602 gypsum Inorganic materials 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000004438 haloalkoxy group Chemical group 0.000 description 1
- 229910001385 heavy metal Inorganic materials 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 125000005842 heteroatom Chemical group 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 238000003898 horticulture Methods 0.000 description 1
- 150000007857 hydrazones Chemical class 0.000 description 1
- 150000002431 hydrogen Chemical class 0.000 description 1
- REYJJPSVUYRZGE-UHFFFAOYSA-O hydron;octadecan-1-amine Chemical compound CCCCCCCCCCCCCCCCCC[NH3+] REYJJPSVUYRZGE-UHFFFAOYSA-O 0.000 description 1
- SHFJWMWCIHQNCP-UHFFFAOYSA-M hydron;tetrabutylazanium;sulfate Chemical compound OS([O-])(=O)=O.CCCC[N+](CCCC)(CCCC)CCCC SHFJWMWCIHQNCP-UHFFFAOYSA-M 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000005764 inhibitory process Effects 0.000 description 1
- 238000013101 initial test Methods 0.000 description 1
- 239000001023 inorganic pigment Substances 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- INQOMBQAUSQDDS-UHFFFAOYSA-N iodomethane Chemical compound IC INQOMBQAUSQDDS-UHFFFAOYSA-N 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- DCYOBGZUOMKFPA-UHFFFAOYSA-N iron(2+);iron(3+);octadecacyanide Chemical compound [Fe+2].[Fe+2].[Fe+2].[Fe+3].[Fe+3].[Fe+3].[Fe+3].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-].N#[C-] DCYOBGZUOMKFPA-UHFFFAOYSA-N 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- 230000001418 larval effect Effects 0.000 description 1
- 229920005610 lignin Polymers 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 239000004579 marble Substances 0.000 description 1
- 150000002731 mercury compounds Chemical class 0.000 description 1
- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical class C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- AHYIWWMFQYBLOY-UHFFFAOYSA-N methyl n-[4-[[[2-chloro-4-(trifluoromethoxy)benzoyl]-ethylamino]-(3,3-dimethylbutan-2-yl)carbamoyl]phenyl]carbamate Chemical compound C=1C=C(OC(F)(F)F)C=C(Cl)C=1C(=O)N(CC)N(C(C)C(C)(C)C)C(=O)C1=CC=C(NC(=O)OC)C=C1 AHYIWWMFQYBLOY-UHFFFAOYSA-N 0.000 description 1
- JHVZCFBUPCLVLL-UHFFFAOYSA-N methyl n-[4-[[[2-chloro-4-(trifluoromethoxy)benzoyl]-methylamino]-(3,3-dimethylbutan-2-yl)carbamoyl]phenyl]carbamate Chemical compound C1=CC(NC(=O)OC)=CC=C1C(=O)N(C(C)C(C)(C)C)N(C)C(=O)C1=CC=C(OC(F)(F)F)C=C1Cl JHVZCFBUPCLVLL-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003595 mist Substances 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- YNAVUWVOSKDBBP-UHFFFAOYSA-O morpholinium Chemical compound [H+].C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-O 0.000 description 1
- OAWIRWKPSSAAQG-UHFFFAOYSA-N n',4-ditert-butyl-n'-(4-tert-butylbenzoyl)-n-ethylbenzohydrazide Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C(C)(C)C)C=C1 OAWIRWKPSSAAQG-UHFFFAOYSA-N 0.000 description 1
- RYGVSYSVVUEDJL-UHFFFAOYSA-N n',4-ditert-butyl-n'-(4-tert-butylbenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C(C)(C)C)C=C1 RYGVSYSVVUEDJL-UHFFFAOYSA-N 0.000 description 1
- GPXSLAGFIDUFCU-UHFFFAOYSA-N n',n'-dibenzoylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)NN(C(=O)C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 GPXSLAGFIDUFCU-UHFFFAOYSA-N 0.000 description 1
- HXAITTUONQDOKF-UHFFFAOYSA-N n'-(2-aminobenzoyl)-n-butan-2-yl-3,4-dichloro-n'-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C(Cl)=CC=1C(=O)N(C(C)CC)N(CC)C(=O)C1=CC=CC=C1N HXAITTUONQDOKF-UHFFFAOYSA-N 0.000 description 1
- SBQLAVDHRMIHJC-UHFFFAOYSA-N n'-(2-aminobenzoyl)-n-butan-2-yl-3,4-dichloro-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C(Cl)=CC=1C(=O)N(C(C)CC)N(C)C(=O)C1=CC=CC=C1N SBQLAVDHRMIHJC-UHFFFAOYSA-N 0.000 description 1
- PHTROUOCORPUFL-UHFFFAOYSA-N n'-(4-acetylbenzenecarbothioyl)-3,4-dichloro-n-(3,3-dimethylbutan-2-yl)-n'-ethylbenzohydrazide Chemical compound C=1C=C(C(C)=O)C=CC=1C(=S)N(CC)N(C(C)C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 PHTROUOCORPUFL-UHFFFAOYSA-N 0.000 description 1
- PEDDKPWLPDMNFR-UHFFFAOYSA-N n'-(4-acetylbenzenecarbothioyl)-3,4-dichloro-n-(3,3-dimethylbutan-2-yl)-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C(Cl)=CC=1C(=O)N(C(C)C(C)(C)C)N(C)C(=S)C1=CC=C(C(C)=O)C=C1 PEDDKPWLPDMNFR-UHFFFAOYSA-N 0.000 description 1
- GCQWZRUNSJAZFV-UHFFFAOYSA-N n'-(4-anilinobenzoyl)-n'-tert-butyl-2,3,4,5,6-pentafluoro-n-methylbenzohydrazide Chemical compound FC=1C(F)=C(F)C(F)=C(F)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C(C=C1)=CC=C1NC1=CC=CC=C1 GCQWZRUNSJAZFV-UHFFFAOYSA-N 0.000 description 1
- NWAALVMGBYTRHJ-UHFFFAOYSA-N n'-(4-anilinobenzoyl)-n'-tert-butyl-n-ethyl-2,3,4,5,6-pentafluorobenzohydrazide Chemical compound FC=1C(F)=C(F)C(F)=C(F)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C(C=C1)=CC=C1NC1=CC=CC=C1 NWAALVMGBYTRHJ-UHFFFAOYSA-N 0.000 description 1
- XKWXFDSIZGNUNG-UHFFFAOYSA-N n'-(4-benzoylbenzoyl)-6-bromo-n'-tert-butyl-n-ethylnaphthalene-2-carbohydrazide Chemical compound C=1C=C2C=C(Br)C=CC2=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C(C=C1)=CC=C1C(=O)C1=CC=CC=C1 XKWXFDSIZGNUNG-UHFFFAOYSA-N 0.000 description 1
- KMLSQFFZYDAEIZ-UHFFFAOYSA-N n'-(4-benzoylbenzoyl)-6-bromo-n'-tert-butyl-n-methylnaphthalene-2-carbohydrazide Chemical compound C=1C=C2C=C(Br)C=CC2=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C(C=C1)=CC=C1C(=O)C1=CC=CC=C1 KMLSQFFZYDAEIZ-UHFFFAOYSA-N 0.000 description 1
- TULGYQNBXXMGCN-UHFFFAOYSA-N n'-(4-bromobenzoyl)-n'-[(2,4-dichlorophenyl)methyl]-n-(3,3-dimethylbutan-2-yl)-3-methylbenzohydrazide Chemical compound C=1C=CC(C)=CC=1C(=O)N(C(C)C(C)(C)C)N(C(=O)C=1C=CC(Br)=CC=1)CC1=CC=C(Cl)C=C1Cl TULGYQNBXXMGCN-UHFFFAOYSA-N 0.000 description 1
- KHOQCPPHTJCNCY-UHFFFAOYSA-N n'-(4-ethylbenzoyl)-3-methyl-n'-[(3-nitrophenyl)methyl]-n-propan-2-ylbenzohydrazide Chemical compound C1=CC(CC)=CC=C1C(=O)N(N(C(C)C)C(=O)C=1C=C(C)C=CC=1)CC1=CC=CC([N+]([O-])=O)=C1 KHOQCPPHTJCNCY-UHFFFAOYSA-N 0.000 description 1
- LFENQWXGFMADOU-UHFFFAOYSA-N n'-[3-(benzenesulfonyl)benzoyl]-3,4-dichloro-n-(3,3-dimethylbutan-2-yl)-n'-ethylbenzohydrazide Chemical compound C=1C=CC(S(=O)(=O)C=2C=CC=CC=2)=CC=1C(=O)N(CC)N(C(C)C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 LFENQWXGFMADOU-UHFFFAOYSA-N 0.000 description 1
- DVHOYBDRLNCATP-UHFFFAOYSA-N n'-[3-(benzenesulfonyl)benzoyl]-3,4-dichloro-n-(3,3-dimethylbutan-2-yl)-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C(Cl)=CC=1C(=O)N(C(C)C(C)(C)C)N(C)C(=O)C(C=1)=CC=CC=1S(=O)(=O)C1=CC=CC=C1 DVHOYBDRLNCATP-UHFFFAOYSA-N 0.000 description 1
- DOKUCVZILGCEES-UHFFFAOYSA-N n'-acetyl-n'-(4-nitrophenyl)benzohydrazide Chemical compound C=1C=C([N+]([O-])=O)C=CC=1N(C(=O)C)NC(=O)C1=CC=CC=C1 DOKUCVZILGCEES-UHFFFAOYSA-N 0.000 description 1
- MPZNENBFTADWFN-UHFFFAOYSA-N n'-benzoyl-2-bromo-4-chloro-n'-ethyl-n-propan-2-ylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)C)C(=O)C1=CC=C(Cl)C=C1Br MPZNENBFTADWFN-UHFFFAOYSA-N 0.000 description 1
- TZHJQUBMAJBBAO-UHFFFAOYSA-N n'-benzoyl-2-bromo-4-chloro-n'-methyl-n-propan-2-ylbenzohydrazide Chemical compound C=1C=C(Cl)C=C(Br)C=1C(=O)N(C(C)C)N(C)C(=O)C1=CC=CC=C1 TZHJQUBMAJBBAO-UHFFFAOYSA-N 0.000 description 1
- JHGOGMOHUVLLKH-UHFFFAOYSA-N n'-benzoyl-2-bromo-n-tert-butyl-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1Br JHGOGMOHUVLLKH-UHFFFAOYSA-N 0.000 description 1
- KQZLPLNLFACPSE-UHFFFAOYSA-N n'-benzoyl-2-bromo-n-tert-butyl-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1Br KQZLPLNLFACPSE-UHFFFAOYSA-N 0.000 description 1
- TUBXNJZJFZCING-UHFFFAOYSA-N n'-benzoyl-4-methoxy-n-(methylsulfanylmethyl)-n'-propan-2-ylbenzohydrazide Chemical compound C1=CC(OC)=CC=C1C(=O)N(CSC)N(C(C)C)C(=O)C1=CC=CC=C1 TUBXNJZJFZCING-UHFFFAOYSA-N 0.000 description 1
- DYBNOPFECZSFBU-UHFFFAOYSA-N n'-benzoyl-n',4-ditert-butyl-n-ethylbenzohydrazide Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 DYBNOPFECZSFBU-UHFFFAOYSA-N 0.000 description 1
- MZYKHSPYOBJOSE-UHFFFAOYSA-N n'-benzoyl-n',4-ditert-butyl-n-methylbenzohydrazide Chemical compound C=1C=C(C(C)(C)C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1 MZYKHSPYOBJOSE-UHFFFAOYSA-N 0.000 description 1
- QLFORKOADGIJGQ-UHFFFAOYSA-N n'-benzoyl-n'-(cyclohexylmethyl)benzohydrazide Chemical class C=1C=CC=CC=1C(=O)NN(C(=O)C=1C=CC=CC=1)CC1CCCCC1 QLFORKOADGIJGQ-UHFFFAOYSA-N 0.000 description 1
- MARKSEVIQATWPC-UHFFFAOYSA-N n'-benzoyl-n'-butan-2-yl-n-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)CC)N(CC)C(=O)C1=CC=CC=C1 MARKSEVIQATWPC-UHFFFAOYSA-N 0.000 description 1
- MXWYIOMDKWDLFO-UHFFFAOYSA-N n'-benzoyl-n'-butan-2-yl-n-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)CC)N(C)C(=O)C1=CC=CC=C1 MXWYIOMDKWDLFO-UHFFFAOYSA-N 0.000 description 1
- BPFADLIZCSFOBZ-UHFFFAOYSA-N n'-benzoyl-n'-phenylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)NN(C=1C=CC=CC=1)C(=O)C1=CC=CC=C1 BPFADLIZCSFOBZ-UHFFFAOYSA-N 0.000 description 1
- JAIVUQYHHYXGAG-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-2-chloro-n-ethylbenzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 JAIVUQYHHYXGAG-UHFFFAOYSA-N 0.000 description 1
- ZXXIDXXVEPQYGA-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-2-chloro-n-methylbenzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1 ZXXIDXXVEPQYGA-UHFFFAOYSA-N 0.000 description 1
- KOMRBIKNWGKPRT-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-3-chloro-n-ethylbenzohydrazide Chemical compound C=1C=CC(Cl)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 KOMRBIKNWGKPRT-UHFFFAOYSA-N 0.000 description 1
- GGJXXPZHCMYKDK-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-3-chloro-n-methylbenzohydrazide Chemical compound C=1C=CC(Cl)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1 GGJXXPZHCMYKDK-UHFFFAOYSA-N 0.000 description 1
- KULGHHRTSBPGQC-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-4-chloro-n-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 KULGHHRTSBPGQC-UHFFFAOYSA-N 0.000 description 1
- AWKSFWPXMMNAGV-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-4-chloro-n-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1 AWKSFWPXMMNAGV-UHFFFAOYSA-N 0.000 description 1
- BJECYTSEMQOYIV-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n,2-dimethylbenzohydrazide Chemical compound C=1C=CC=C(C)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1 BJECYTSEMQOYIV-UHFFFAOYSA-N 0.000 description 1
- FZCIABQCGNDNKV-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n,4-dimethylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1 FZCIABQCGNDNKV-UHFFFAOYSA-N 0.000 description 1
- QEWRKTKZIKTXHT-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n-ethyl-2-methylbenzohydrazide Chemical compound C=1C=CC=C(C)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 QEWRKTKZIKTXHT-UHFFFAOYSA-N 0.000 description 1
- BTAKBKYGJUIYRR-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n-ethyl-4-methylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 BTAKBKYGJUIYRR-UHFFFAOYSA-N 0.000 description 1
- OSJRWXOEJSXPIO-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 OSJRWXOEJSXPIO-UHFFFAOYSA-N 0.000 description 1
- TVPFNNODRLVIHY-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n-ethylnaphthalene-1-carbohydrazide Chemical compound C=1C=CC2=CC=CC=C2C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1 TVPFNNODRLVIHY-UHFFFAOYSA-N 0.000 description 1
- NDAWKNDITUJPGO-UHFFFAOYSA-N n'-benzoyl-n'-tert-butyl-n-methylnaphthalene-1-carbohydrazide Chemical compound C=1C=CC2=CC=CC=C2C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1 NDAWKNDITUJPGO-UHFFFAOYSA-N 0.000 description 1
- XOIXDRVCBOULDT-UHFFFAOYSA-N n'-benzoyl-n,n'-bis(2-methylpropyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC(C)C)N(CC(C)C)C(=O)C1=CC=CC=C1 XOIXDRVCBOULDT-UHFFFAOYSA-N 0.000 description 1
- GKQUBXMQSJPMDC-UHFFFAOYSA-N n'-benzoyl-n-ethyl-n'-(2-methylpropyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(CC(C)C)C(=O)C1=CC=CC=C1 GKQUBXMQSJPMDC-UHFFFAOYSA-N 0.000 description 1
- UZQUYEMJIPLICV-UHFFFAOYSA-N n'-benzoyl-n-ethyl-n'-(3-methylbutan-2-yl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)C(C)C)C(=O)C1=CC=CC=C1 UZQUYEMJIPLICV-UHFFFAOYSA-N 0.000 description 1
- PPENJPLNCPSHGN-UHFFFAOYSA-N n'-benzoyl-n-ethyl-n'-propan-2-ylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)C)C(=O)C1=CC=CC=C1 PPENJPLNCPSHGN-UHFFFAOYSA-N 0.000 description 1
- JEJHKVUAKXHHCZ-UHFFFAOYSA-N n'-benzoyl-n-methyl-n'-(2-methylpropyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC(C)C)N(C)C(=O)C1=CC=CC=C1 JEJHKVUAKXHHCZ-UHFFFAOYSA-N 0.000 description 1
- ZSBSDDFESIBNQH-UHFFFAOYSA-N n'-benzoyl-n-methyl-n'-propan-2-ylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C(C)C)N(C)C(=O)C1=CC=CC=C1 ZSBSDDFESIBNQH-UHFFFAOYSA-N 0.000 description 1
- KFTRIELCTAPNRQ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2,3-dichloro-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1Cl KFTRIELCTAPNRQ-UHFFFAOYSA-N 0.000 description 1
- MQKYGTVSZLNKAW-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2,3-dichloro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1Cl MQKYGTVSZLNKAW-UHFFFAOYSA-N 0.000 description 1
- CNJZDNOJUAZOEC-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2,4-dichloro-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl CNJZDNOJUAZOEC-UHFFFAOYSA-N 0.000 description 1
- XZERYYAGWKSILR-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2,4-dichloro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl XZERYYAGWKSILR-UHFFFAOYSA-N 0.000 description 1
- VTUYZBLHDHRBHF-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2,5-difluoro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC(F)=CC=C1F VTUYZBLHDHRBHF-UHFFFAOYSA-N 0.000 description 1
- LWVICUUWTXYFIW-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2,6-dichloro-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=C(Cl)C=CC=C1Cl LWVICUUWTXYFIW-UHFFFAOYSA-N 0.000 description 1
- ZPZVENSKXUNZMT-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2,6-dichloro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=C(Cl)C=CC=C1Cl ZPZVENSKXUNZMT-UHFFFAOYSA-N 0.000 description 1
- QEPOHRZRLUYWCB-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2,6-difluoro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=C(F)C=CC=C1F QEPOHRZRLUYWCB-UHFFFAOYSA-N 0.000 description 1
- PWJVMLLIAIKSJR-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2-chloro-n',5-dimethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC(C)=CC=C1Cl PWJVMLLIAIKSJR-UHFFFAOYSA-N 0.000 description 1
- SXATYQXFXSLGDE-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2-chloro-n'-ethyl-4-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C=C1Cl SXATYQXFXSLGDE-UHFFFAOYSA-N 0.000 description 1
- CLGZCLOZMOBQNH-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2-chloro-n'-ethyl-5-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC(C)=CC=C1Cl CLGZCLOZMOBQNH-UHFFFAOYSA-N 0.000 description 1
- NAZJVNRAMXXPGH-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2-chloro-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1Cl NAZJVNRAMXXPGH-UHFFFAOYSA-N 0.000 description 1
- JVBMEVRABHRCJO-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2-chloro-n'-methyl-4-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C=C1Cl JVBMEVRABHRCJO-UHFFFAOYSA-N 0.000 description 1
- FRUSPCPWKDIJDP-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2-chloro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1Cl FRUSPCPWKDIJDP-UHFFFAOYSA-N 0.000 description 1
- PVPWPHXOWGUUMU-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2-fluoro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1F PVPWPHXOWGUUMU-UHFFFAOYSA-N 0.000 description 1
- URWZHIICVBENOO-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-2-methoxy-n'-methylbenzohydrazide Chemical compound COC1=CC=CC=C1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=CC=C1 URWZHIICVBENOO-UHFFFAOYSA-N 0.000 description 1
- HDQBMWCAHALGBV-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3,4-dichloro-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 HDQBMWCAHALGBV-UHFFFAOYSA-N 0.000 description 1
- PGHPQQNEJOPAGC-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3,4-dichloro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 PGHPQQNEJOPAGC-UHFFFAOYSA-N 0.000 description 1
- WWKURCORCBWMHM-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3,5-dichloro-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC(Cl)=CC(Cl)=C1 WWKURCORCBWMHM-UHFFFAOYSA-N 0.000 description 1
- JSVJLRXJEHSDOP-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3,5-dichloro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC(Cl)=CC(Cl)=C1 JSVJLRXJEHSDOP-UHFFFAOYSA-N 0.000 description 1
- RIQWCSUNJYMQFI-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3,5-dimethylbenzohydrazide Chemical compound CC1=CC(C)=CC(C(=O)N(NC(=O)C=2C=CC=CC=2)C(C)(C)C)=C1 RIQWCSUNJYMQFI-UHFFFAOYSA-N 0.000 description 1
- BZULZMCDVMNADG-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-chloro-n',2-dimethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1C BZULZMCDVMNADG-UHFFFAOYSA-N 0.000 description 1
- OQYACXIOKJDWSE-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-chloro-n',4-dimethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C)C(Cl)=C1 OQYACXIOKJDWSE-UHFFFAOYSA-N 0.000 description 1
- KVLWAXUXYUWSEM-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-chloro-n'-ethyl-2-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1C KVLWAXUXYUWSEM-UHFFFAOYSA-N 0.000 description 1
- VMDIESSPBUZVLV-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-chloro-n'-ethyl-2-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1[N+]([O-])=O VMDIESSPBUZVLV-UHFFFAOYSA-N 0.000 description 1
- FFDRAOQFWAZMGP-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-chloro-n'-ethyl-4-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C)C(Cl)=C1 FFDRAOQFWAZMGP-UHFFFAOYSA-N 0.000 description 1
- QXKWKRROLKFWON-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-chloro-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1 QXKWKRROLKFWON-UHFFFAOYSA-N 0.000 description 1
- UDLKJLOOEMPGPH-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-chloro-n'-methyl-2-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1[N+]([O-])=O UDLKJLOOEMPGPH-UHFFFAOYSA-N 0.000 description 1
- CJXBROGNVIKGKH-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-chloro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1 CJXBROGNVIKGKH-UHFFFAOYSA-N 0.000 description 1
- NFWDZJGLHOAWQC-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-cyano-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(C#N)=C1 NFWDZJGLHOAWQC-UHFFFAOYSA-N 0.000 description 1
- OFAMBUOFPCNAJF-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-cyano-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(C#N)=C1 OFAMBUOFPCNAJF-UHFFFAOYSA-N 0.000 description 1
- RSOQIQVFSPCJGZ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-fluoro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(F)=C1 RSOQIQVFSPCJGZ-UHFFFAOYSA-N 0.000 description 1
- DDMIXYRREGQOOR-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-methoxy-n'-methyl-2-nitrobenzohydrazide Chemical compound COC1=CC=CC(C(=O)N(N(C)C(=O)C=2C=CC=CC=2)C(C)(C)C)=C1[N+]([O-])=O DDMIXYRREGQOOR-UHFFFAOYSA-N 0.000 description 1
- SSHILUSSTHFDEX-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-methoxy-n'-methyl-4-nitrobenzohydrazide Chemical compound C1=C([N+]([O-])=O)C(OC)=CC(C(=O)N(N(C)C(=O)C=2C=CC=CC=2)C(C)(C)C)=C1 SSHILUSSTHFDEX-UHFFFAOYSA-N 0.000 description 1
- JJSHTADGOKCFQR-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-3-methoxy-n'-methylbenzohydrazide Chemical compound COC1=CC=CC(C(=O)N(N(C)C(=O)C=2C=CC=CC=2)C(C)(C)C)=C1 JJSHTADGOKCFQR-UHFFFAOYSA-N 0.000 description 1
- IKQUUQUTTHRICC-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-butyl-n'-ethylbenzohydrazide Chemical compound C1=CC(CCCC)=CC=C1C(=O)N(C(C)(C)C)N(CC)C(=O)C1=CC=CC=C1 IKQUUQUTTHRICC-UHFFFAOYSA-N 0.000 description 1
- GIFSXALOLPMEQE-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-butyl-n'-methylbenzohydrazide Chemical compound C1=CC(CCCC)=CC=C1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=CC=C1 GIFSXALOLPMEQE-UHFFFAOYSA-N 0.000 description 1
- DNTUBOXSDIIXST-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-chloro-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1 DNTUBOXSDIIXST-UHFFFAOYSA-N 0.000 description 1
- LVVHSOFIAHCJSQ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-chloro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1 LVVHSOFIAHCJSQ-UHFFFAOYSA-N 0.000 description 1
- HWBXLUBEUROUBM-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-cyano-n'-ethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C#N)C=C1 HWBXLUBEUROUBM-UHFFFAOYSA-N 0.000 description 1
- PRTWSAYKQLZPBO-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-cyano-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C#N)C=C1 PRTWSAYKQLZPBO-UHFFFAOYSA-N 0.000 description 1
- CVDLWTYXPKDWPE-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-ethyl-n'-methylbenzohydrazide Chemical compound C1=CC(CC)=CC=C1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=CC=C1 CVDLWTYXPKDWPE-UHFFFAOYSA-N 0.000 description 1
- UNNNVBUBZVFTCH-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-fluoro-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(F)C=C1 UNNNVBUBZVFTCH-UHFFFAOYSA-N 0.000 description 1
- ZOJNLLJWZBQPBQ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-hydroxy-n'-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(O)C=C1 ZOJNLLJWZBQPBQ-UHFFFAOYSA-N 0.000 description 1
- KZWZTJPLBPRNDI-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-4-methoxy-n'-methylbenzohydrazide Chemical compound C1=CC(OC)=CC=C1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=CC=C1 KZWZTJPLBPRNDI-UHFFFAOYSA-N 0.000 description 1
- KNMABLJZWMIYFZ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n',2-dimethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1C KNMABLJZWMIYFZ-UHFFFAOYSA-N 0.000 description 1
- FHIZLJSLVYNDBG-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n',3,5-trimethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 FHIZLJSLVYNDBG-UHFFFAOYSA-N 0.000 description 1
- MYXLOYCSSHPQLL-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n',3-dimethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 MYXLOYCSSHPQLL-UHFFFAOYSA-N 0.000 description 1
- DUCGZKHCTQSWFB-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n',4-diethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(CC)C=C1 DUCGZKHCTQSWFB-UHFFFAOYSA-N 0.000 description 1
- LRXJLSKBVLAEKL-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n',4-dimethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C)C=C1 LRXJLSKBVLAEKL-UHFFFAOYSA-N 0.000 description 1
- DRWRPHWABSQYSI-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n',5-dimethyl-2-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC(C)=CC=C1[N+]([O-])=O DRWRPHWABSQYSI-UHFFFAOYSA-N 0.000 description 1
- SBPDJERECFFUOL-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-2,4-dinitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O SBPDJERECFFUOL-UHFFFAOYSA-N 0.000 description 1
- DEMSKXNGHJKVTF-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-2,5-difluorobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC(F)=CC=C1F DEMSKXNGHJKVTF-UHFFFAOYSA-N 0.000 description 1
- SPELDOIMWKYOQJ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-2,6-difluorobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=C(F)C=CC=C1F SPELDOIMWKYOQJ-UHFFFAOYSA-N 0.000 description 1
- KLNNIJSKYYLBOR-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-2-(trifluoromethyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1C(F)(F)F KLNNIJSKYYLBOR-UHFFFAOYSA-N 0.000 description 1
- AKVAWQNSHWQHTN-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-2-fluorobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1F AKVAWQNSHWQHTN-UHFFFAOYSA-N 0.000 description 1
- XGSJTAOQGBHJLJ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-2-methoxybenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1OC XGSJTAOQGBHJLJ-UHFFFAOYSA-N 0.000 description 1
- QKDWWTMLTLLCPE-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-2-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1C QKDWWTMLTLLCPE-UHFFFAOYSA-N 0.000 description 1
- UWEUHGLVWUVHFD-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-2-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O UWEUHGLVWUVHFD-UHFFFAOYSA-N 0.000 description 1
- MHOLXITYTYICHB-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3,5-dimethylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 MHOLXITYTYICHB-UHFFFAOYSA-N 0.000 description 1
- RHPXTFBKTFCIIL-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3,5-dinitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 RHPXTFBKTFCIIL-UHFFFAOYSA-N 0.000 description 1
- AFSKHGCCNWYRON-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3-(trifluoromethyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(C(F)(F)F)=C1 AFSKHGCCNWYRON-UHFFFAOYSA-N 0.000 description 1
- XVUUTQTZDNEVEP-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3-fluorobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(F)=C1 XVUUTQTZDNEVEP-UHFFFAOYSA-N 0.000 description 1
- NGHRIFOMRJEWPC-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3-methoxy-2-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(OC)=C1[N+]([O-])=O NGHRIFOMRJEWPC-UHFFFAOYSA-N 0.000 description 1
- VFBZJDLWRCJFCI-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3-methoxy-4-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C(OC)=C1 VFBZJDLWRCJFCI-UHFFFAOYSA-N 0.000 description 1
- KDFGGIVIVWZBJZ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3-methoxybenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(OC)=C1 KDFGGIVIVWZBJZ-UHFFFAOYSA-N 0.000 description 1
- HMPBXZSJGXOGOL-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 HMPBXZSJGXOGOL-UHFFFAOYSA-N 0.000 description 1
- SIHULEKJVHYLQL-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-3-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC([N+]([O-])=O)=C1 SIHULEKJVHYLQL-UHFFFAOYSA-N 0.000 description 1
- OCPCKMUXIRTZPC-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-4-(trifluoromethyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C(F)(F)F)C=C1 OCPCKMUXIRTZPC-UHFFFAOYSA-N 0.000 description 1
- QRBACHGTWIECHA-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-4-fluorobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(F)C=C1 QRBACHGTWIECHA-UHFFFAOYSA-N 0.000 description 1
- CAOIPAABQNWSOG-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-4-hydroxybenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(O)C=C1 CAOIPAABQNWSOG-UHFFFAOYSA-N 0.000 description 1
- KFCVRYSDZXIETD-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-4-methoxybenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(OC)C=C1 KFCVRYSDZXIETD-UHFFFAOYSA-N 0.000 description 1
- UGDNLSOZCNKKDB-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-4-methylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C)C=C1 UGDNLSOZCNKKDB-UHFFFAOYSA-N 0.000 description 1
- SEKHVBGUDGEZPE-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-4-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C=C1 SEKHVBGUDGEZPE-UHFFFAOYSA-N 0.000 description 1
- LLELRKKBMUMJCU-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-4-propan-2-ylbenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C(C)C)C=C1 LLELRKKBMUMJCU-UHFFFAOYSA-N 0.000 description 1
- DDQWGWVPCYQYFN-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-ethyl-5-methyl-2-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC(C)=CC=C1[N+]([O-])=O DDQWGWVPCYQYFN-UHFFFAOYSA-N 0.000 description 1
- GNBVLYCXLAKYRA-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-2,4-dinitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O GNBVLYCXLAKYRA-UHFFFAOYSA-N 0.000 description 1
- CHJKXXKLABWVSJ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-2-(trifluoromethyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1C(F)(F)F CHJKXXKLABWVSJ-UHFFFAOYSA-N 0.000 description 1
- XWXAAQKMJNDOQM-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-2-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O XWXAAQKMJNDOQM-UHFFFAOYSA-N 0.000 description 1
- TUFINSRWYOMEFA-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-3,5-dinitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 TUFINSRWYOMEFA-UHFFFAOYSA-N 0.000 description 1
- HGILRPVWXZAOOZ-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-3-(trifluoromethyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(C(F)(F)F)=C1 HGILRPVWXZAOOZ-UHFFFAOYSA-N 0.000 description 1
- GCFZYYLXDQOLNF-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-3-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC([N+]([O-])=O)=C1 GCFZYYLXDQOLNF-UHFFFAOYSA-N 0.000 description 1
- ZKFIDIFDMQWMFW-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-4-(trifluoromethyl)benzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C(F)(F)F)C=C1 ZKFIDIFDMQWMFW-UHFFFAOYSA-N 0.000 description 1
- MYVYUNMNQJPNFS-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-4-nitrobenzohydrazide Chemical compound C=1C=CC=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C=C1 MYVYUNMNQJPNFS-UHFFFAOYSA-N 0.000 description 1
- IWEKXPXJXTVWSC-UHFFFAOYSA-N n'-benzoyl-n-tert-butyl-n'-methyl-4-propan-2-ylbenzohydrazide Chemical compound C1=CC(C(C)C)=CC=C1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=CC=C1 IWEKXPXJXTVWSC-UHFFFAOYSA-N 0.000 description 1
- KVIFVIVCKWOPEY-UHFFFAOYSA-N n'-butan-2-yl-3-chloro-n-ethyl-n'-(3-phenyldiazenylbenzoyl)-5-sulfanylbenzohydrazide Chemical compound C=1C=CC(N=NC=2C=CC=CC=2)=CC=1C(=O)N(C(C)CC)N(CC)C(=O)C1=CC(S)=CC(Cl)=C1 KVIFVIVCKWOPEY-UHFFFAOYSA-N 0.000 description 1
- QNDMYKHNSNAOTR-UHFFFAOYSA-N n'-butan-2-yl-3-chloro-n-methyl-n'-(3-phenyldiazenylbenzoyl)-5-sulfanylbenzohydrazide Chemical compound C=1C=CC(N=NC=2C=CC=CC=2)=CC=1C(=O)N(C(C)CC)N(C)C(=O)C1=CC(S)=CC(Cl)=C1 QNDMYKHNSNAOTR-UHFFFAOYSA-N 0.000 description 1
- HDOBEKYBGKSUTN-UHFFFAOYSA-N n'-ethyl-3-nitro-n'-(4-pent-2-ynoylbenzoyl)-n-propan-2-ylbenzohydrazide Chemical compound C1=CC(C(=O)C#CCC)=CC=C1C(=O)N(CC)N(C(C)C)C(=O)C1=CC=CC([N+]([O-])=O)=C1 HDOBEKYBGKSUTN-UHFFFAOYSA-N 0.000 description 1
- SMWVOACEQKAQSS-UHFFFAOYSA-N n'-ethyl-n'-[4-(4-methylpentan-2-yl)benzoyl]-2-nitro-n-propan-2-ylbenzohydrazide Chemical compound C=1C=C(C(C)CC(C)C)C=CC=1C(=O)N(CC)N(C(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O SMWVOACEQKAQSS-UHFFFAOYSA-N 0.000 description 1
- OLLXKLIFAJYVCT-UHFFFAOYSA-N n'-methyl-3-nitro-n'-(4-pent-2-ynoylbenzoyl)-n-propan-2-ylbenzohydrazide Chemical compound C1=CC(C(=O)C#CCC)=CC=C1C(=O)N(C)N(C(C)C)C(=O)C1=CC=CC([N+]([O-])=O)=C1 OLLXKLIFAJYVCT-UHFFFAOYSA-N 0.000 description 1
- FWNBRONUHBKYNG-UHFFFAOYSA-N n'-methyl-n'-[4-(4-methylpentan-2-yl)benzoyl]-2-nitro-n-propan-2-ylbenzohydrazide Chemical compound C1=CC(C(C)CC(C)C)=CC=C1C(=O)N(C)N(C(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O FWNBRONUHBKYNG-UHFFFAOYSA-N 0.000 description 1
- DQHVTYRLXVDVMJ-UHFFFAOYSA-N n'-tert-butyl-2,3,4-trichloro-n-ethyl-n'-(2-nitrobenzoyl)benzohydrazide Chemical compound C=1C=C(Cl)C(Cl)=C(Cl)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O DQHVTYRLXVDVMJ-UHFFFAOYSA-N 0.000 description 1
- YJFHOACDPZJOSP-UHFFFAOYSA-N n'-tert-butyl-2,3,4-trichloro-n-methyl-n'-(2-nitrobenzoyl)benzohydrazide Chemical compound C=1C=C(Cl)C(Cl)=C(Cl)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O YJFHOACDPZJOSP-UHFFFAOYSA-N 0.000 description 1
- ROHYKVOOEAOGGG-UHFFFAOYSA-N n'-tert-butyl-2,4-dichloro-n-ethyl-n'-[4-(trifluoromethoxy)benzoyl]benzohydrazide Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(OC(F)(F)F)C=C1 ROHYKVOOEAOGGG-UHFFFAOYSA-N 0.000 description 1
- HYRVRKGUGUOVOF-UHFFFAOYSA-N n'-tert-butyl-2,4-dichloro-n-methyl-n'-[4-(trifluoromethoxy)benzoyl]benzohydrazide Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(OC(F)(F)F)C=C1 HYRVRKGUGUOVOF-UHFFFAOYSA-N 0.000 description 1
- DOSALRFTEIKWJS-UHFFFAOYSA-N n'-tert-butyl-2,5-dichloro-n-ethyl-n'-(4-trimethylsilylbenzoyl)benzohydrazide Chemical compound C=1C(Cl)=CC=C(Cl)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C([Si](C)(C)C)C=C1 DOSALRFTEIKWJS-UHFFFAOYSA-N 0.000 description 1
- WYNXPMXNZIMTJP-UHFFFAOYSA-N n'-tert-butyl-2,5-dichloro-n-methyl-n'-(4-trimethylsilylbenzoyl)benzohydrazide Chemical compound C=1C(Cl)=CC=C(Cl)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C([Si](C)(C)C)C=C1 WYNXPMXNZIMTJP-UHFFFAOYSA-N 0.000 description 1
- DMMXKVZAVAZTJI-UHFFFAOYSA-N n'-tert-butyl-2-chloro-n'-(2-chlorobenzoyl)-n-[(3,5-dinitrophenyl)methyl]benzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(C(C)(C)C)N(C(=O)C=1C(=CC=CC=1)Cl)CC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1 DMMXKVZAVAZTJI-UHFFFAOYSA-N 0.000 description 1
- ULDUUQCFVKBIDJ-UHFFFAOYSA-N n'-tert-butyl-2-chloro-n'-(2-chlorobenzoyl)-n-ethylbenzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1Cl ULDUUQCFVKBIDJ-UHFFFAOYSA-N 0.000 description 1
- AOLWBUCLJBIENG-UHFFFAOYSA-N n'-tert-butyl-2-chloro-n'-(2-chlorobenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1Cl AOLWBUCLJBIENG-UHFFFAOYSA-N 0.000 description 1
- DKQKASYRERGUHI-UHFFFAOYSA-N n'-tert-butyl-2-chloro-n'-(3-methylbenzoyl)-n-(methylsulfanylmethyl)benzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(CSC)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 DKQKASYRERGUHI-UHFFFAOYSA-N 0.000 description 1
- LLKZWDZRVDNCTN-UHFFFAOYSA-N n'-tert-butyl-2-fluoro-n'-(2-fluorobenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=CC=C(F)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1F LLKZWDZRVDNCTN-UHFFFAOYSA-N 0.000 description 1
- LAFMVZCCHVCRJO-UHFFFAOYSA-N n'-tert-butyl-2-methoxy-n'-(2-methoxybenzoyl)-n-methylbenzohydrazide Chemical compound COC1=CC=CC=C1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1OC LAFMVZCCHVCRJO-UHFFFAOYSA-N 0.000 description 1
- BEBPMKUPXAATOI-UHFFFAOYSA-N n'-tert-butyl-3,4-dichloro-n'-(3,4-dichlorobenzoyl)-n-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C(Cl)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 BEBPMKUPXAATOI-UHFFFAOYSA-N 0.000 description 1
- NAUGEBNIWNVUKZ-UHFFFAOYSA-N n'-tert-butyl-3,4-dichloro-n'-(3,4-dichlorobenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=C(Cl)C(Cl)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 NAUGEBNIWNVUKZ-UHFFFAOYSA-N 0.000 description 1
- YIFWUIULRAEJHA-UHFFFAOYSA-N n'-tert-butyl-3-chloro-n'-(3-chlorobenzoyl)-n-ethylbenzohydrazide Chemical compound C=1C=CC(Cl)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1 YIFWUIULRAEJHA-UHFFFAOYSA-N 0.000 description 1
- XTCDKCPLKLYLCA-UHFFFAOYSA-N n'-tert-butyl-3-chloro-n'-(3-chlorobenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=CC(Cl)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1 XTCDKCPLKLYLCA-UHFFFAOYSA-N 0.000 description 1
- ZRRRVIMPSSLUNE-UHFFFAOYSA-N n'-tert-butyl-3-ethanethioyl-n-ethyl-n'-[4-(1,1,2,2,2-pentafluoroethoxy)benzoyl]benzohydrazide Chemical compound C=1C=CC(C(C)=S)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(OC(F)(F)C(F)(F)F)C=C1 ZRRRVIMPSSLUNE-UHFFFAOYSA-N 0.000 description 1
- PCTCRYOINMGPEX-UHFFFAOYSA-N n'-tert-butyl-3-ethanethioyl-n-methyl-n'-[4-(1,1,2,2,2-pentafluoroethoxy)benzoyl]benzohydrazide Chemical compound C=1C=CC(C(C)=S)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(OC(F)(F)C(F)(F)F)C=C1 PCTCRYOINMGPEX-UHFFFAOYSA-N 0.000 description 1
- QFVOYMOSQSXEOK-UHFFFAOYSA-N n'-tert-butyl-3-fluoro-n'-(3-fluorobenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=CC(F)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(F)=C1 QFVOYMOSQSXEOK-UHFFFAOYSA-N 0.000 description 1
- HXUIGWWXXFUBSJ-UHFFFAOYSA-N n'-tert-butyl-3-methoxy-n'-(3-methoxybenzoyl)-n-methylbenzohydrazide Chemical compound COC1=CC=CC(C(=O)N(C)N(C(=O)C=2C=C(OC)C=CC=2)C(C)(C)C)=C1 HXUIGWWXXFUBSJ-UHFFFAOYSA-N 0.000 description 1
- FUMXPHWXMOOAAA-UHFFFAOYSA-N n'-tert-butyl-4-chloro-n'-(4-chlorobenzoyl)-n-(methylsulfanylmethyl)benzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CSC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1 FUMXPHWXMOOAAA-UHFFFAOYSA-N 0.000 description 1
- VFIPIQJZAUKDLT-UHFFFAOYSA-N n'-tert-butyl-4-chloro-n'-(4-chlorobenzoyl)-n-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1 VFIPIQJZAUKDLT-UHFFFAOYSA-N 0.000 description 1
- YANDJDIBHDWMJB-UHFFFAOYSA-N n'-tert-butyl-4-chloro-n'-(4-chlorobenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1 YANDJDIBHDWMJB-UHFFFAOYSA-N 0.000 description 1
- FMDJEDZCQUKNMA-UHFFFAOYSA-N n'-tert-butyl-4-chloro-n-ethyl-n'-[4-(methylamino)benzoyl]-2-(trifluoromethoxy)benzohydrazide Chemical compound C=1C=C(Cl)C=C(OC(F)(F)F)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(NC)C=C1 FMDJEDZCQUKNMA-UHFFFAOYSA-N 0.000 description 1
- NYWNVDDDWKEVCP-UHFFFAOYSA-N n'-tert-butyl-4-chloro-n-methyl-n'-[4-(methylamino)benzoyl]-2-(trifluoromethoxy)benzohydrazide Chemical compound C1=CC(NC)=CC=C1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=C(Cl)C=C1OC(F)(F)F NYWNVDDDWKEVCP-UHFFFAOYSA-N 0.000 description 1
- YMAFXHFTKAMLNV-UHFFFAOYSA-N n'-tert-butyl-4-cyano-n'-(4-cyanobenzoyl)-n-ethylbenzohydrazide Chemical compound C=1C=C(C#N)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C#N)C=C1 YMAFXHFTKAMLNV-UHFFFAOYSA-N 0.000 description 1
- BAGVAIZMMMUKAX-UHFFFAOYSA-N n'-tert-butyl-4-cyano-n'-(4-cyanobenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=C(C#N)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C#N)C=C1 BAGVAIZMMMUKAX-UHFFFAOYSA-N 0.000 description 1
- IEIWXLVYWUCZRS-UHFFFAOYSA-N n'-tert-butyl-4-fluoro-n'-(4-fluorobenzoyl)-n-methylbenzohydrazide Chemical compound C=1C=C(F)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(F)C=C1 IEIWXLVYWUCZRS-UHFFFAOYSA-N 0.000 description 1
- IOEJJHRKVHNJET-UHFFFAOYSA-N n'-tert-butyl-4-methoxy-n'-(4-methoxybenzoyl)-n-methylbenzohydrazide Chemical compound C1=CC(OC)=CC=C1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(OC)C=C1 IOEJJHRKVHNJET-UHFFFAOYSA-N 0.000 description 1
- VVGDJWYGGVBUBM-UHFFFAOYSA-N n'-tert-butyl-n'-(4-chlorobenzoyl)-n,4-dimethylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1 VVGDJWYGGVBUBM-UHFFFAOYSA-N 0.000 description 1
- QXLGJJPCAYHBKA-UHFFFAOYSA-N n'-tert-butyl-n'-(4-chlorobenzoyl)-n-(methoxymethyl)-4-propylbenzohydrazide Chemical compound C1=CC(CCC)=CC=C1C(=O)N(COC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1 QXLGJJPCAYHBKA-UHFFFAOYSA-N 0.000 description 1
- FAVPXPIKUNIEBT-UHFFFAOYSA-N n'-tert-butyl-n'-(4-chlorobenzoyl)-n-ethyl-4-methylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1 FAVPXPIKUNIEBT-UHFFFAOYSA-N 0.000 description 1
- NPDONHZTYYACNT-UHFFFAOYSA-N n'-tert-butyl-n'-(4-ethynylbenzoyl)-n,4-dimethylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C#C)C=C1 NPDONHZTYYACNT-UHFFFAOYSA-N 0.000 description 1
- DYXUQFRMKLMTFN-UHFFFAOYSA-N n'-tert-butyl-n'-(4-fluorobenzoyl)-n,4-dimethylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(F)C=C1 DYXUQFRMKLMTFN-UHFFFAOYSA-N 0.000 description 1
- BYWRVXJQOXJWNJ-UHFFFAOYSA-N n'-tert-butyl-n'-(4-fluorobenzoyl)-n-methyl-3-(1,2,2-trichloroethenyl)benzohydrazide Chemical compound C=1C=CC(C(Cl)=C(Cl)Cl)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(F)C=C1 BYWRVXJQOXJWNJ-UHFFFAOYSA-N 0.000 description 1
- PHZIQPRRHIUCAD-UHFFFAOYSA-N n'-tert-butyl-n,2-dimethyl-n'-(2-methylbenzoyl)benzohydrazide Chemical compound C=1C=CC=C(C)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1C PHZIQPRRHIUCAD-UHFFFAOYSA-N 0.000 description 1
- XJTPQPXPKXWCMX-UHFFFAOYSA-N n'-tert-butyl-n,3-dimethyl-n'-(3-methylbenzoyl)benzohydrazide Chemical compound C=1C=CC(C)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 XJTPQPXPKXWCMX-UHFFFAOYSA-N 0.000 description 1
- OHVBUTPRWMKXTN-UHFFFAOYSA-N n'-tert-butyl-n,4-dimethyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C)C=C1 OHVBUTPRWMKXTN-UHFFFAOYSA-N 0.000 description 1
- AEFGXMJVMWSBPS-UHFFFAOYSA-N n'-tert-butyl-n,4-dimethyl-n'-[4-(trifluoromethyl)benzoyl]benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C(F)(F)F)C=C1 AEFGXMJVMWSBPS-UHFFFAOYSA-N 0.000 description 1
- FWWPKYWDPKDQSG-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-2-fluoro-n'-(2-fluorobenzoyl)benzohydrazide Chemical compound C=1C=CC=C(F)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1F FWWPKYWDPKDQSG-UHFFFAOYSA-N 0.000 description 1
- KPHICMKXXWHKSJ-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-2-methoxy-n'-(2-methoxybenzoyl)benzohydrazide Chemical compound C=1C=CC=C(OC)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1OC KPHICMKXXWHKSJ-UHFFFAOYSA-N 0.000 description 1
- FVBZYLYZYVDHQZ-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-2-methyl-n'-(2-methylbenzoyl)benzohydrazide Chemical compound C=1C=CC=C(C)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1C FVBZYLYZYVDHQZ-UHFFFAOYSA-N 0.000 description 1
- VNQVXCJJGCJNKB-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-2-nitro-n'-(2-nitrobenzoyl)benzohydrazide Chemical compound C=1C=CC=C([N+]([O-])=O)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O VNQVXCJJGCJNKB-UHFFFAOYSA-N 0.000 description 1
- RWTLQZJOCUSOSL-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-3-fluoro-n'-(3-fluorobenzoyl)benzohydrazide Chemical compound C=1C=CC(F)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(F)=C1 RWTLQZJOCUSOSL-UHFFFAOYSA-N 0.000 description 1
- YZPODTDMUZIOOF-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-3-methoxy-n'-(3-methoxybenzoyl)benzohydrazide Chemical compound C=1C=CC(OC)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(OC)=C1 YZPODTDMUZIOOF-UHFFFAOYSA-N 0.000 description 1
- MBIWFFVAVTXGOH-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-3-methyl-n'-(3-methylbenzoyl)benzohydrazide Chemical compound C=1C=CC(C)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 MBIWFFVAVTXGOH-UHFFFAOYSA-N 0.000 description 1
- ZXBAUGIVCQQIPO-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-3-nitro-n'-(3-nitrobenzoyl)benzohydrazide Chemical compound C=1C=CC([N+]([O-])=O)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC([N+]([O-])=O)=C1 ZXBAUGIVCQQIPO-UHFFFAOYSA-N 0.000 description 1
- NTOKXJNYUXPOPF-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-4-fluoro-n'-(4-fluorobenzoyl)benzohydrazide Chemical compound C=1C=C(F)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(F)C=C1 NTOKXJNYUXPOPF-UHFFFAOYSA-N 0.000 description 1
- CJRNGHMFCFMRMB-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-4-methoxy-n'-(4-methoxybenzoyl)benzohydrazide Chemical compound C=1C=C(OC)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(OC)C=C1 CJRNGHMFCFMRMB-UHFFFAOYSA-N 0.000 description 1
- PHRXJXSKEQKGQQ-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-4-methyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C)C=C1 PHRXJXSKEQKGQQ-UHFFFAOYSA-N 0.000 description 1
- ULMKHENZNCFGGN-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-4-methyl-n'-[4-(trifluoromethyl)benzoyl]benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C(F)(F)F)C=C1 ULMKHENZNCFGGN-UHFFFAOYSA-N 0.000 description 1
- YLTBDBZDZQRTPV-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-4-nitro-n'-(4-nitrobenzoyl)benzohydrazide Chemical compound C=1C=C([N+]([O-])=O)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C=C1 YLTBDBZDZQRTPV-UHFFFAOYSA-N 0.000 description 1
- URPDUPXRBJNHRR-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-n'-(4-ethynylbenzoyl)-4-methylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C#C)C=C1 URPDUPXRBJNHRR-UHFFFAOYSA-N 0.000 description 1
- OVLJAMJAAHGGEI-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-n'-(4-fluorobenzoyl)-3-(1,2,2-trichloroethenyl)benzohydrazide Chemical compound C=1C=CC(C(Cl)=C(Cl)Cl)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(F)C=C1 OVLJAMJAAHGGEI-UHFFFAOYSA-N 0.000 description 1
- VVSHVLDRVGVNTL-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-n'-(4-fluorobenzoyl)-4-methylbenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(F)C=C1 VVSHVLDRVGVNTL-UHFFFAOYSA-N 0.000 description 1
- VOJHXZXFRGCFAL-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-n'-(naphthalene-1-carbonyl)naphthalene-1-carbohydrazide Chemical compound C1=CC=C2C(C(=O)N(N(C(=O)C=3C4=CC=CC=C4C=CC=3)C(C)(C)C)CC)=CC=CC2=C1 VOJHXZXFRGCFAL-UHFFFAOYSA-N 0.000 description 1
- ZFPTXSNBWKAIFP-UHFFFAOYSA-N n'-tert-butyl-n-ethyl-n'-(naphthalene-2-carbonyl)naphthalene-2-carbohydrazide Chemical compound C1=CC=CC2=CC(C(=O)N(N(C(=O)C=3C=C4C=CC=CC4=CC=3)C(C)(C)C)CC)=CC=C21 ZFPTXSNBWKAIFP-UHFFFAOYSA-N 0.000 description 1
- NTFZPVFEOTXGIF-UHFFFAOYSA-N n'-tert-butyl-n-methyl-2-nitro-n'-(2-nitrobenzoyl)benzohydrazide Chemical compound C=1C=CC=C([N+]([O-])=O)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O NTFZPVFEOTXGIF-UHFFFAOYSA-N 0.000 description 1
- SWDBPVYCJTWQNN-UHFFFAOYSA-N n'-tert-butyl-n-methyl-3-nitro-n'-(3-nitrobenzoyl)benzohydrazide Chemical compound C=1C=CC([N+]([O-])=O)=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC([N+]([O-])=O)=C1 SWDBPVYCJTWQNN-UHFFFAOYSA-N 0.000 description 1
- AMRYTCLGXABQNA-UHFFFAOYSA-N n'-tert-butyl-n-methyl-4-nitro-n'-(4-nitrobenzoyl)benzohydrazide Chemical compound C=1C=C([N+]([O-])=O)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C([N+]([O-])=O)C=C1 AMRYTCLGXABQNA-UHFFFAOYSA-N 0.000 description 1
- LZIAZDKVGDYAQX-UHFFFAOYSA-N n'-tert-butyl-n-methyl-n'-(naphthalene-1-carbonyl)naphthalene-1-carbohydrazide Chemical compound C1=CC=C2C(C(=O)N(N(C(=O)C=3C4=CC=CC=C4C=CC=3)C(C)(C)C)C)=CC=CC2=C1 LZIAZDKVGDYAQX-UHFFFAOYSA-N 0.000 description 1
- GSEKHUWXPCTPPK-UHFFFAOYSA-N n'-tert-butyl-n-methyl-n'-(naphthalene-2-carbonyl)naphthalene-2-carbohydrazide Chemical compound C1=CC=CC2=CC(C(=O)N(N(C(=O)C=3C=C4C=CC=CC4=CC=3)C(C)(C)C)C)=CC=C21 GSEKHUWXPCTPPK-UHFFFAOYSA-N 0.000 description 1
- HYEIEPNTTXKNSG-UHFFFAOYSA-N n,n,2-trimethyl-5-[methyl-[propan-2-yl-[4-(trifluoromethyl)benzoyl]amino]carbamoyl]benzamide Chemical compound C=1C=C(C(F)(F)F)C=CC=1C(=O)N(C(C)C)N(C)C(=O)C1=CC=C(C)C(C(=O)N(C)C)=C1 HYEIEPNTTXKNSG-UHFFFAOYSA-N 0.000 description 1
- GJPYPVQPKBBIIC-UHFFFAOYSA-N n-[4-[tert-butyl-[[2-(2-chlorophenyl)benzoyl]-methylamino]carbamoyl]-2-chlorophenyl]acetamide Chemical compound C=1C=CC=C(C=2C(=CC=CC=2)Cl)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(NC(C)=O)C(Cl)=C1 GJPYPVQPKBBIIC-UHFFFAOYSA-N 0.000 description 1
- XOYCMKCWPZGINZ-UHFFFAOYSA-N n-[4-[tert-butyl-[[4-(dimethylamino)benzoyl]-ethylamino]carbamoyl]phenyl]acetamide Chemical compound C=1C=C(N(C)C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(NC(C)=O)C=C1 XOYCMKCWPZGINZ-UHFFFAOYSA-N 0.000 description 1
- OKFNZSBUTAEKLW-UHFFFAOYSA-N n-[4-[tert-butyl-[[4-(dimethylamino)benzoyl]-methylamino]carbamoyl]phenyl]acetamide Chemical compound C1=CC(N(C)C)=CC=C1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(NC(C)=O)C=C1 OKFNZSBUTAEKLW-UHFFFAOYSA-N 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- AIAMRLHGZUTLLB-UHFFFAOYSA-N n-ethyl-3-(hydroxyamino)-n'-propan-2-yl-n'-[4-(tribromomethyl)benzoyl]benzohydrazide Chemical compound C=1C=CC(NO)=CC=1C(=O)N(CC)N(C(C)C)C(=O)C1=CC=C(C(Br)(Br)Br)C=C1 AIAMRLHGZUTLLB-UHFFFAOYSA-N 0.000 description 1
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- VIAXSXRJKRNPGT-UHFFFAOYSA-N n-tert-butyl-2,4-dichloro-n'-(2-chlorobenzoyl)-n'-(methoxymethyl)benzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(COC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl VIAXSXRJKRNPGT-UHFFFAOYSA-N 0.000 description 1
- UBHCTBCGTVFZOB-UHFFFAOYSA-N n-tert-butyl-2,4-dichloro-n'-(4-chlorobenzoyl)-n'-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl UBHCTBCGTVFZOB-UHFFFAOYSA-N 0.000 description 1
- XWOMIGPKXGONBU-UHFFFAOYSA-N n-tert-butyl-2,4-dichloro-n'-(4-chlorobenzoyl)-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl XWOMIGPKXGONBU-UHFFFAOYSA-N 0.000 description 1
- UDZVGECHTHOBNC-UHFFFAOYSA-N n-tert-butyl-2,4-dichloro-n'-ethyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl UDZVGECHTHOBNC-UHFFFAOYSA-N 0.000 description 1
- FXORWCDBROMOBZ-UHFFFAOYSA-N n-tert-butyl-2,4-dichloro-n'-ethyl-n'-(4-nitrosobenzoyl)benzohydrazide Chemical compound C=1C=C(N=O)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl FXORWCDBROMOBZ-UHFFFAOYSA-N 0.000 description 1
- PGMVAHABAUCHOW-UHFFFAOYSA-N n-tert-butyl-2,4-dichloro-n'-methyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl PGMVAHABAUCHOW-UHFFFAOYSA-N 0.000 description 1
- VESZXHUDWFYUMH-UHFFFAOYSA-N n-tert-butyl-2,4-dichloro-n'-methyl-n'-(4-nitrosobenzoyl)benzohydrazide Chemical compound C=1C=C(N=O)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1Cl VESZXHUDWFYUMH-UHFFFAOYSA-N 0.000 description 1
- CIZMSYUPPFVZNE-UHFFFAOYSA-N n-tert-butyl-2-chloro-n'-(4-chlorobenzoyl)-n'-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1Cl CIZMSYUPPFVZNE-UHFFFAOYSA-N 0.000 description 1
- IRPXOOYNAXHIMG-UHFFFAOYSA-N n-tert-butyl-2-chloro-n'-(4-chlorobenzoyl)-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1Cl IRPXOOYNAXHIMG-UHFFFAOYSA-N 0.000 description 1
- RZSQBGYCFBEWLZ-UHFFFAOYSA-N n-tert-butyl-2-chloro-n'-ethyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1Cl RZSQBGYCFBEWLZ-UHFFFAOYSA-N 0.000 description 1
- AFDDFXOUCVYPLV-UHFFFAOYSA-N n-tert-butyl-2-chloro-n'-methyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1Cl AFDDFXOUCVYPLV-UHFFFAOYSA-N 0.000 description 1
- XJIKLBIBELPWHV-UHFFFAOYSA-N n-tert-butyl-3,4,5-trimethoxy-n'-methyl-n'-(3-methylsulfinylbenzoyl)benzohydrazide Chemical compound COC1=C(OC)C(OC)=CC(C(=O)N(N(C)C(=O)C=2C=C(C=CC=2)S(C)=O)C(C)(C)C)=C1 XJIKLBIBELPWHV-UHFFFAOYSA-N 0.000 description 1
- ODIXRODTXUKFKW-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-(2-chlorobenzoyl)-n'-ethylbenzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 ODIXRODTXUKFKW-UHFFFAOYSA-N 0.000 description 1
- NRXTWMMZZJJIIB-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-(2-chlorobenzoyl)-n'-methylbenzohydrazide Chemical compound C=1C=CC=C(Cl)C=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 NRXTWMMZZJJIIB-UHFFFAOYSA-N 0.000 description 1
- ZZYTXOMURPMRNS-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-(4-chlorobenzoyl)-n'-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 ZZYTXOMURPMRNS-UHFFFAOYSA-N 0.000 description 1
- BEWCGTIYPYJCSI-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-(4-chlorobenzoyl)-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 BEWCGTIYPYJCSI-UHFFFAOYSA-N 0.000 description 1
- FEBQRFMWVBUVEK-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-ethyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 FEBQRFMWVBUVEK-UHFFFAOYSA-N 0.000 description 1
- ZOEOBGYCMADPNQ-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-ethyl-n'-(4-propylbenzenecarbothioyl)benzohydrazide Chemical compound C1=CC(CCC)=CC=C1C(=S)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 ZOEOBGYCMADPNQ-UHFFFAOYSA-N 0.000 description 1
- JVRRQVQNWKRBQA-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-methyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 JVRRQVQNWKRBQA-UHFFFAOYSA-N 0.000 description 1
- XGYZRPMBDMLKFX-UHFFFAOYSA-N n-tert-butyl-3,4-dichloro-n'-methyl-n'-(4-propylbenzenecarbothioyl)benzohydrazide Chemical compound C1=CC(CCC)=CC=C1C(=S)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C(Cl)=C1 XGYZRPMBDMLKFX-UHFFFAOYSA-N 0.000 description 1
- DUSVPFRGCFTLFY-UHFFFAOYSA-N n-tert-butyl-3,5-dichloro-n'-(4-chlorobenzoyl)-n'-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC(Cl)=CC(Cl)=C1 DUSVPFRGCFTLFY-UHFFFAOYSA-N 0.000 description 1
- FCKFEZGTZZYLLK-UHFFFAOYSA-N n-tert-butyl-3,5-dichloro-n'-(4-chlorobenzoyl)-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC(Cl)=CC(Cl)=C1 FCKFEZGTZZYLLK-UHFFFAOYSA-N 0.000 description 1
- UZOOWONFTCUBBT-UHFFFAOYSA-N n-tert-butyl-3,5-dichloro-n'-(4-ethenylbenzoyl)-n'-(methoxymethyl)benzohydrazide Chemical compound C=1C=C(C=C)C=CC=1C(=O)N(COC)N(C(C)(C)C)C(=O)C1=CC(Cl)=CC(Cl)=C1 UZOOWONFTCUBBT-UHFFFAOYSA-N 0.000 description 1
- ZWUQFLSXRTUBRF-UHFFFAOYSA-N n-tert-butyl-3,5-dichloro-n'-(4-iodobenzoyl)-n'-(methoxymethyl)benzohydrazide Chemical compound C=1C=C(I)C=CC=1C(=O)N(COC)N(C(C)(C)C)C(=O)C1=CC(Cl)=CC(Cl)=C1 ZWUQFLSXRTUBRF-UHFFFAOYSA-N 0.000 description 1
- AIFNNLGCLKUKRF-UHFFFAOYSA-N n-tert-butyl-3,5-dichloro-n'-ethyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC(Cl)=CC(Cl)=C1 AIFNNLGCLKUKRF-UHFFFAOYSA-N 0.000 description 1
- ZZYWZNQSJGOSKE-UHFFFAOYSA-N n-tert-butyl-3,5-dichloro-n'-methyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC(Cl)=CC(Cl)=C1 ZZYWZNQSJGOSKE-UHFFFAOYSA-N 0.000 description 1
- IETFKLYBLBTXCX-UHFFFAOYSA-N n-tert-butyl-3-chloro-n'-ethyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1 IETFKLYBLBTXCX-UHFFFAOYSA-N 0.000 description 1
- YGINDSDNFYDKFQ-UHFFFAOYSA-N n-tert-butyl-3-chloro-n'-methyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(Cl)=C1 YGINDSDNFYDKFQ-UHFFFAOYSA-N 0.000 description 1
- ZJFDZPFQHSHRKX-UHFFFAOYSA-N n-tert-butyl-4-chloro-2-(difluoromethoxy)-n'-(4-ethylbenzoyl)-n'-methylbenzohydrazide Chemical compound C1=CC(CC)=CC=C1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1OC(F)F ZJFDZPFQHSHRKX-UHFFFAOYSA-N 0.000 description 1
- HFMZVCMUWNPRAV-UHFFFAOYSA-N n-tert-butyl-4-chloro-2-(difluoromethoxy)-n'-ethyl-n'-(4-ethylbenzoyl)benzohydrazide Chemical compound C=1C=C(CC)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(Cl)C=C1OC(F)F HFMZVCMUWNPRAV-UHFFFAOYSA-N 0.000 description 1
- LBWMARVHOFICAB-UHFFFAOYSA-N n-tert-butyl-n',2-dimethyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1C LBWMARVHOFICAB-UHFFFAOYSA-N 0.000 description 1
- FBPYOZLNSKCMDN-UHFFFAOYSA-N n-tert-butyl-n',3-dimethyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 FBPYOZLNSKCMDN-UHFFFAOYSA-N 0.000 description 1
- HYKIEMKIRHXUOI-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-3-methoxy-n'-methylbenzohydrazide Chemical compound COC1=CC=CC(C(=O)N(N(C)C(=O)C=2C=CC(Cl)=CC=2)C(C)(C)C)=C1 HYKIEMKIRHXUOI-UHFFFAOYSA-N 0.000 description 1
- NFGXUBIMGIZRCB-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-4-(chloromethyl)-n'-ethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(CCl)C=C1 NFGXUBIMGIZRCB-UHFFFAOYSA-N 0.000 description 1
- ZLMYXGPZSQNHSO-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-4-(chloromethyl)-n'-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(CCl)C=C1 ZLMYXGPZSQNHSO-UHFFFAOYSA-N 0.000 description 1
- GFBQPKWLYZIOOA-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n',2-dimethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1C GFBQPKWLYZIOOA-UHFFFAOYSA-N 0.000 description 1
- DIQLZGJNMVRRRM-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n',3-dimethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 DIQLZGJNMVRRRM-UHFFFAOYSA-N 0.000 description 1
- CGDQNGYIRSWJMB-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n',4-dimethylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C)C=C1 CGDQNGYIRSWJMB-UHFFFAOYSA-N 0.000 description 1
- YSPFPQVRZMLXJY-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n'-ethyl-2-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1C YSPFPQVRZMLXJY-UHFFFAOYSA-N 0.000 description 1
- MFPIGEDYHDYQPB-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n'-ethyl-3-methoxybenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(OC)=C1 MFPIGEDYHDYQPB-UHFFFAOYSA-N 0.000 description 1
- MBDDBGDPTQYKEQ-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n'-ethyl-3-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 MBDDBGDPTQYKEQ-UHFFFAOYSA-N 0.000 description 1
- BWIACRAOYCSAPC-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n'-ethyl-4-(trifluoromethyl)benzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C(F)(F)F)C=C1 BWIACRAOYCSAPC-UHFFFAOYSA-N 0.000 description 1
- DDNIZAFAWPNQOO-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n'-ethyl-4-methylbenzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(C)C=C1 DDNIZAFAWPNQOO-UHFFFAOYSA-N 0.000 description 1
- PYFIFWQTCLURLW-UHFFFAOYSA-N n-tert-butyl-n'-(4-chlorobenzoyl)-n'-methyl-4-(trifluoromethyl)benzohydrazide Chemical compound C=1C=C(Cl)C=CC=1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(C(F)(F)F)C=C1 PYFIFWQTCLURLW-UHFFFAOYSA-N 0.000 description 1
- AAMFXEONEBPTCA-UHFFFAOYSA-N n-tert-butyl-n'-(4-ethylbenzoyl)-3,5-dimethyl-n'-prop-2-ynylbenzohydrazide Chemical compound C1=CC(CC)=CC=C1C(=O)N(CC#C)N(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 AAMFXEONEBPTCA-UHFFFAOYSA-N 0.000 description 1
- XSULVEGUNCVBFH-UHFFFAOYSA-N n-tert-butyl-n'-(4-methylbenzoyl)-2-nitro-n'-(phenylsulfanylmethyl)benzohydrazide Chemical compound C1=CC(C)=CC=C1C(=O)N(N(C(=O)C=1C(=CC=CC=1)[N+]([O-])=O)C(C)(C)C)CSC1=CC=CC=C1 XSULVEGUNCVBFH-UHFFFAOYSA-N 0.000 description 1
- IPDZGBCSMNZAOL-UHFFFAOYSA-N n-tert-butyl-n'-(4-methylbenzoyl)-n'-(methylsulfanylmethyl)-2-nitrobenzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CSC)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O IPDZGBCSMNZAOL-UHFFFAOYSA-N 0.000 description 1
- LMRGXGCNZHGPIO-UHFFFAOYSA-N n-tert-butyl-n'-[4-(1-hydroxyprop-2-ynyl)benzoyl]-n'-methyl-1,3-benzodioxole-5-carbohydrazide Chemical compound C=1C=C2OCOC2=CC=1C(=O)N(C(C)(C)C)N(C)C(=O)C1=CC=C(C(O)C#C)C=C1 LMRGXGCNZHGPIO-UHFFFAOYSA-N 0.000 description 1
- UYUIWXYGFKOMGU-UHFFFAOYSA-N n-tert-butyl-n'-ethyl-2-methyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1C UYUIWXYGFKOMGU-UHFFFAOYSA-N 0.000 description 1
- YJFNJZIPUDBTBS-UHFFFAOYSA-N n-tert-butyl-n'-ethyl-3,4,5-trimethoxy-n'-(3-methylsulfinylbenzoyl)benzohydrazide Chemical compound C=1C=CC(S(C)=O)=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC(OC)=C(OC)C(OC)=C1 YJFNJZIPUDBTBS-UHFFFAOYSA-N 0.000 description 1
- WVZBNYBWOOAWMV-UHFFFAOYSA-N n-tert-butyl-n'-ethyl-3-methyl-n'-(4-methylbenzoyl)benzohydrazide Chemical compound C=1C=C(C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC(C)=C1 WVZBNYBWOOAWMV-UHFFFAOYSA-N 0.000 description 1
- XTHCJXCHTBWYLS-UHFFFAOYSA-N n-tert-butyl-n'-ethyl-4-pent-4-enyl-n'-(4-propanoylbenzoyl)benzohydrazide Chemical compound C=1C=C(C(=O)CC)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=C(CCCC=C)C=C1 XTHCJXCHTBWYLS-UHFFFAOYSA-N 0.000 description 1
- GVKRKUVROKZYCA-UHFFFAOYSA-N n-tert-butyl-n'-ethyl-n'-[4-(1-hydroxyprop-2-ynyl)benzoyl]-1,3-benzodioxole-5-carbohydrazide Chemical compound C=1C=C2OCOC2=CC=1C(=O)N(C(C)(C)C)N(CC)C(=O)C1=CC=C(C(O)C#C)C=C1 GVKRKUVROKZYCA-UHFFFAOYSA-N 0.000 description 1
- JCKQCNZDZVUKQK-UHFFFAOYSA-N n-tert-butyl-n'-ethyl-n'-[4-(2-methylpropyl)benzoyl]-2-nitrobenzohydrazide Chemical compound C=1C=C(CC(C)C)C=CC=1C(=O)N(CC)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O JCKQCNZDZVUKQK-UHFFFAOYSA-N 0.000 description 1
- BQFGHYURTHJRQM-UHFFFAOYSA-N n-tert-butyl-n'-methyl-4-pent-4-enyl-n'-(4-propanoylbenzoyl)benzohydrazide Chemical compound C1=CC(C(=O)CC)=CC=C1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=C(CCCC=C)C=C1 BQFGHYURTHJRQM-UHFFFAOYSA-N 0.000 description 1
- YWDXYXPYSVQRQR-UHFFFAOYSA-N n-tert-butyl-n'-methyl-n'-[4-(2-methylpropyl)benzoyl]-2-nitrobenzohydrazide Chemical compound C1=CC(CC(C)C)=CC=C1C(=O)N(C)N(C(C)(C)C)C(=O)C1=CC=CC=C1[N+]([O-])=O YWDXYXPYSVQRQR-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 239000011368 organic material Substances 0.000 description 1
- 150000002903 organophosphorus compounds Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-M perchlorate Inorganic materials [O-]Cl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-M 0.000 description 1
- VLTRZXGMWDSKGL-UHFFFAOYSA-N perchloric acid Chemical compound OCl(=O)(=O)=O VLTRZXGMWDSKGL-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000003209 petroleum derivative Substances 0.000 description 1
- 239000003444 phase transfer catalyst Substances 0.000 description 1
- 229940096826 phenylmercuric acetate Drugs 0.000 description 1
- ZAEQTGTVGUJEFV-UHFFFAOYSA-N phenylmethanesulfonate;pyridin-1-ium Chemical compound C1=CC=[NH+]C=C1.[O-]S(=O)(=O)CC1=CC=CC=C1 ZAEQTGTVGUJEFV-UHFFFAOYSA-N 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 239000001007 phthalocyanine dye Substances 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- 229960005235 piperonyl butoxide Drugs 0.000 description 1
- 230000007096 poisonous effect Effects 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- VKJKEPKFPUWCAS-UHFFFAOYSA-M potassium chlorate Chemical compound [K+].[O-]Cl(=O)=O VKJKEPKFPUWCAS-UHFFFAOYSA-M 0.000 description 1
- 229910000105 potassium hydride Inorganic materials 0.000 description 1
- NTTOTNSKUYCDAV-UHFFFAOYSA-N potassium hydride Chemical compound [KH] NTTOTNSKUYCDAV-UHFFFAOYSA-N 0.000 description 1
- LPNYRYFBWFDTMA-UHFFFAOYSA-N potassium tert-butoxide Chemical group [K+].CC(C)(C)[O-] LPNYRYFBWFDTMA-UHFFFAOYSA-N 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 230000002062 proliferating effect Effects 0.000 description 1
- JKANAVGODYYCQF-UHFFFAOYSA-N prop-2-yn-1-amine Chemical compound NCC#C JKANAVGODYYCQF-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- YORCIIVHUBAYBQ-UHFFFAOYSA-N propargyl bromide Chemical compound BrCC#C YORCIIVHUBAYBQ-UHFFFAOYSA-N 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- 239000011814 protection agent Substances 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- JUJWROOIHBZHMG-UHFFFAOYSA-O pyridinium Chemical compound C1=CC=[NH+]C=C1 JUJWROOIHBZHMG-UHFFFAOYSA-O 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 150000003252 quinoxalines Chemical class 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000003128 rodenticide Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 229910052682 stishovite Inorganic materials 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- UXQPRXPNOJXOQO-UHFFFAOYSA-N sulfuric acid;hydrobromide Chemical compound Br.OS(O)(=O)=O UXQPRXPNOJXOQO-UHFFFAOYSA-N 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 239000012747 synergistic agent Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000002641 tar oil Substances 0.000 description 1
- LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 description 1
- CXINFVCBBRIKAQ-UHFFFAOYSA-N tert-butyl 4-[[[4-chloro-3-(trifluoromethoxy)benzoyl]-(2,2-dimethylpropyl)amino]-ethylcarbamoyl]benzoate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1C(=O)N(CC)N(CC(C)(C)C)C(=O)C1=CC=C(Cl)C(OC(F)(F)F)=C1 CXINFVCBBRIKAQ-UHFFFAOYSA-N 0.000 description 1
- OMNTUNHENRXJJV-UHFFFAOYSA-N tert-butyl 4-[[[4-chloro-3-(trifluoromethoxy)benzoyl]-(2,2-dimethylpropyl)amino]-methylcarbamoyl]benzoate Chemical compound C=1C=C(C(=O)OC(C)(C)C)C=CC=1C(=O)N(C)N(CC(C)(C)C)C(=O)C1=CC=C(Cl)C(OC(F)(F)F)=C1 OMNTUNHENRXJJV-UHFFFAOYSA-N 0.000 description 1
- MUQNAPSBHXFMHT-UHFFFAOYSA-N tert-butylhydrazine Chemical compound CC(C)(C)NN MUQNAPSBHXFMHT-UHFFFAOYSA-N 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 239000010936 titanium Substances 0.000 description 1
- 229910052719 titanium Inorganic materials 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 229910052905 tridymite Inorganic materials 0.000 description 1
- GCRCSLNXFKCFHB-UHFFFAOYSA-N triethyl(hexyl)azanium Chemical compound CCCCCC[N+](CC)(CC)CC GCRCSLNXFKCFHB-UHFFFAOYSA-N 0.000 description 1
- ZMANZCXQSJIPKH-UHFFFAOYSA-O triethylammonium ion Chemical compound CC[NH+](CC)CC ZMANZCXQSJIPKH-UHFFFAOYSA-O 0.000 description 1
- WSFDRHZUAHDHDN-UHFFFAOYSA-N trimethyl-[(4-methylphenyl)methyl]azanium Chemical compound CC1=CC=C(C[N+](C)(C)C)C=C1 WSFDRHZUAHDHDN-UHFFFAOYSA-N 0.000 description 1
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- 230000008016 vaporization Effects 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 235000020234 walnut Nutrition 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 235000015099 wheat brans Nutrition 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-UHFFFAOYSA-L 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/10—Hydrazines
- C07C243/12—Hydrazines having nitrogen atoms of hydrazine groups bound to acyclic carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C243/00—Compounds containing chains of nitrogen atoms singly-bound to each other, e.g. hydrazines, triazanes
- C07C243/24—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids
- C07C243/38—Hydrazines having nitrogen atoms of hydrazine groups acylated by carboxylic acids with acylating carboxyl groups bound to carbon atoms of six-membered aromatic rings
-
- 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
- A01N37/28—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 containing the group; Thio analogues thereof
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Heterocyclic Compounds That Contain Two Or More Ring Oxygen Atoms (AREA)
Claims (12)
1. Insektizid-wirksame Verbindung, nämlich ein
substituiertes Hydrazin der Formel:
worin
X und X' gleich oder verschieden voneinander O, S oder
NR sind,
R¹ ein unsubstituiertes, verzweigtes (C&sub3;-C&sub1;&sub0;)Alkyl
oder ein geradkettiges, mit ein oder zwei der
gleichen oder verschiedenen von (C&sub3;-C&sub6;)Cycloalkyl
substituiertes (C&sub1;-C&sub4;)Alkyl ist,
R² (C&sub1;-C&sub6;)Alkyl, Alkoxyalkyl mit, unabhängig
davon, 1 bis 6 C-Atomen in jedem Alkyl-Rest,
(C&sub1;-C&sub6;)Alkylthioalkyl mit, unabhängig davon, 1
bis 6 C-Atomen in jedem Alkyl-Rest,
(C&sub2;-C&sub6;)Alkenyl, (C&sub2;-C&sub6;)Alkynyl oder
Phen(C&sub1;-C&sub4;)alkyl ist, wo der Phenylring
unsubstituiert oder mit ein bis drei der gleichen
oder verschiedenen von Halogen, Cyano, Nitro,
Hydroxy, (C&sub1;-C&sub4;)Alkyl, Halogen(C&sub1;-C&sub4;)alkyl
(C&sub1;-C&sub4;)Alkoxy, Halogen(C&sub1;-C&sub4;)alkoxy,
Carboxy, (C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, NH&sub2;, NHZ oder NZZ'
substituiert ist,
A und B gleich oder verschieden voneinander
ein unsubstituiertes oder substituiertes Naphthyl,
wo die Substituenten ein bis fünf der gleichen oder
verschiedenen von Halogen, Cyano, Nitro, Hydroxy,
(C&sub1;-C&sub4;)- Alkoxy, C&sub1;-C&sub4;)Alkyl, Carboxy,
(C&sub1;-C&sub4;)Alkoxy- carbonyl, (C&sub1;-C&sub4;)Alkanoyloxy,
NH&sub2;, NHZ oder NZZ' sein können,
ein unsubstituiertes oder substituiertes Phenyl, wo
die Substituenten ein bis fünf der gleichen oder
verschiedenen von Halogen, Nitroso, Nitro, Cyano,
Hydroxy, (C&sub1;-C&sub6;)Alkyl,
Halogen(C&sub1;-C&sub6;)alkyl, Cyano(C&sub1;-C&sub6;)alkyl, (C&sub1;-C&sub6;)Alkoxy,
Halogen(C&sub1;-C&sub6;)alkoxy, Alkoxyalkyl mit,
unabhängig davon, 1 bis 6 C-Atomen in jedem
Alkyl-Rest, Alk- oxyalkoxy mit, unabhängig davon, 1
bis 6 C-Atomen in jedem Alkyl-Rest, einem
-OCO&sub2;R-Rest, (C&sub2;-C&sub6;)- Alkenyl, gegebenenfalls
substituiert mit Halogen, Cyano, (C&sub1;-C&sub4;)Alkyl,
(C&sub1;-C&sub4;)Alkoxy, Halogen(C&sub1;-C&sub4;)alkoxy oder
(C&sub1;-C&sub4;)Alkylthio, (C&sub2;-C&sub6;)Alkenylcarbonyl,
(C&sub2;-C&sub6;)Alkadienyl, (C&sub2;-C&sub6;)Alkynyl,
gegebenenfalls substituiert mit Halogen, Cyano,
Nitro, Hydroxy, (C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy,
Halogen(C&sub1;-C&sub4;)alkoxy oder (C&sub1;-C&sub4;)Alkylthio,
(C&sub2;-C&sub6;)Alkynylcarbonyl, Carboxy, einem
-ZCO&sub2;R'-Rest, einem -COR-Rest,
Halogen(C&sub1;-C&sub6;)alkylcarbonyl,
Cyano(C&sub1;-C&sub6;)alkylcarbonyl, Nitro(C&sub1;-C&sub6;)alkylcarbonyl,
(C&sub1;-C&sub6;)Alkoxycarbonyl,
Halogen(C&sub1;-C&sub6;)alkoxycarbonyl, einem -OCOR-Rest, einem -NRR'-Rest,
Amino, substituiert mit Hydroxy, (C&sub1;-C&sub4;)Alkoxy
- oder (C&sub1;-C&sub4;)Alkylthio- Resten, Phenylamino,
Diphenylamino, einem -CONRR'-Rest, einem -OCONRR'-
Rest, einem -C(NR)NR'-R"-Rest, einem -N=NR-Rest,
Phenylazo, einem -NRCOR'-Rest, einem -NRCO&sub2;R'-Rest,
einem -N(COR)COR'-Rest, einem -OCONRCOR'-Rest,
Sulfhydryl, Halogenthio, Thiocyanato,
(C&sub1;-C&sub6;)Alkylthio, Halogen(C&sub1;-C&sub6;)alkylthio, einem -SOR-
Rest, einem -SO&sub2;R-Rest, Phenylsulfonyl, einem
-OSO&sub2;R-Rest, (C&sub1;-C&sub6;)Halogenalkylsulfonyloxy,
einem -SO&sub2;NRR'-Rest, einem -NRSOR'-Rest, einem
-NRSO&sub2;R '-Rest, einem -CSR-Rest, einem -CS&sub2;R-
Rest, einem -NRCSR'-Rest, einem -SCOR-Rest,
Tri(C&sub1;-C&sub6;)alkylsilyl mit, unabhangig davon, der
genannten Zahl von C-Atomen in jedem Alkyl-Rest, sein
können, ein unsubstituiertes oder substituiertes
Phenyl mit ein bis drei der gleichen oder
verschiedenen von Halogen, Cyano, Nitro, Hydroxy,
(C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy, Carboxy,
(C&sub1;-C&sub4;)Alkoxy- carbonyl, (C&sub1;-C&sub4;)Alkanoyloxy,
NH&sub2;, NHZ oder NZZ', Phenoxy, wo der Phenylring
unsubstituiert oder mit ein bis drei der gleichen
oder verschiedenen von Halogen, Cyano, Nitro,
Hydroxy, (C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy,
Carboxy, (C&sub1;-C&sub4;)Alkoxycarbon- yl,
(C&sub1;-C&sub4;)Alkanoyloxy, NH&sub2;, NHZ oder NZZ'
substituiert ist, Benzoyl, wo der Phenylring
unsubstituiert oder mit ein bis drei der gleichen
oder verschiedenen von Halogen, Cyano, Nitro,
Hydroxy, (C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy,
Carboxy, (C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, NH&sub2;, NHZ oder NZZ' substituiert ist,
Phenoxycarbonyl, wo der Phenylring unsubstituiert
oder mit ein bis drei der gleichen oder verschiedenen
von Halogen, Cyano, Nitro, Hydroxy, (C&sub1;-C&sub4;)Alkyl,
(C&sub1;-C&sub4;)Alkoxy, Carboxy,
(C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, NH&sub2;, NHZ oder
NZZ' substituiert ist, Phenylthio, wo der Phenylring
unsubstituiert oder mit ein bis drei der gleichen
oder verschiedenen von Halogen, Cyano, Nitro,
Hydroxy, (C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy,
Carboxy, (C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, NH&sub2;, NHZ oder NZZ' substituiert ist,
ein -CR=N-R²-Rest, wo R² Hydroxy,
(C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy, -NRR', Phenylamino, -COR,
Carboxy, (C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, Benzoyl, Phenoxycarbonyl oder -CONRR'
ist, sind, oder, wenn zwei benachbarte Positionen auf
dem Phenylring mit Alkoxy-Resten substituiert sind,
diese Reste verbunden sein können, um zusammen mit
den C-Atomen, mit denen sie verknüpft sind, einen 5
- oder 6-gliedrigen Dioxolano- oder
Dioxano-heterocyclischen Ring auszubilden,
wo R, R' und RW Wasserstoff oder (C&sub1;-C&sub6;)Alkyl
sind, Z und Z' (C&sub1;-C&sub6;)Alkyl, plus
N-Triniethylsiloxymethyl-N'-2,2-dimethylpropyl-N-(4-methoxy-3-
chlor-benzoyl)-N'-benzoylhydrazin und
N-Phenylthiomethyl-t-
butyl-N-(4-toluoyl)-N'-(3,4-dichlorbenzoyl)hydrazin
sind, wobei
ausgenommen sind,
oder ein landwirtschaftlich verträgliches Salz davon.
2. Verbindung nach Anspruch 1, worin
X und X' O oder S sind,
R¹ ein unsubstituiertes, verzweigtes (C&sub3;-C&sub8;)Alkyl
ist,
R² (C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy(C&sub1;-C&sub4;)alkyl
mit, unabhängig davon, der angegebenen Anzahl von
C-Atomen in jedem Alkyl-Rest, Methylthiomethyl,
(C&sub2;-C&sub5;)Alkenyl, (C&sub2;-C&sub5;)Alkynyl oder Benzyl
ist, wo der Phenylring unsubstituiert oder mit
Halogen, Nitro, (C&sub1;-C&sub4;)Alkyl oder
(C&sub1;-C&sub4;)Alkoxy substituiert ist, und
A und B gleich oder verschieden voneinander ein
unsubstituiertes Naphthyl,
ein unsubstituiertes oder substituiertes Phenyl,
wo die Substituenten ein bis drei der gleichen
oder verschiedenen von Halogen, Nitro, Cyano,
(C&sub1;-C&sub4;)Alkyl, Halogen(C&sub1;-C&sub4;)alkyl,
Cyano(C&sub1;-C&sub4;)alkyl, (C&sub1;-C&sub4;)Alkoxy,
Halogen(C&sub1;-C&sub4;)alkoxy, einem -COD-Rest,
Carboxy, (C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, (C&sub2;-C&sub6;)Alkenyl,
(C&sub2;-C&sub6;)Alkadienyl, (C&sub2;-C&sub6;)Alkynyl, einem -NDD'-Rest,
Thiocyanato, (C&sub1;-C&sub4;)Alkylthio, einem
-CSD-Rest, einem -CS&sub2;D-Rest, einem -SCOD-Rest,
Tri(C&sub1;-C&sub4;)alkylsilyl mit, unabhängig davon,
der angegebenen Anzahl von C-Atomen in jedem
Alkyl-Rest sein können, ein unsubstituiertes oder
substituiertes Phenyl mit ein bis zwei der
gleichen oder verschiedenen von Halogen, Nitro,
(C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy,
Carboxy,
(C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, NH&sub2;, NHZ oder NZZ', Phenoxy, wo
der Phenylring unsubstituiert oder mit ein oder
zwei der gleichen oder verschiedenen von Halogen,
Nitro, (C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy,
Carboxy, (C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, NH&sub2;, NHZ oder NZZ' substituiert
ist, sind, oder wenn zwei benachbarte Positionen
auf dem Phenylring mit Alkoxy-Resten substituiert
sind, diese Reste zur Ausbildung eines 5- oder
6-gliedrigen Dioxolano- oder
Dioxano-heterocyclischen Ring verbunden sein können,
wo D und D' Wasserstoff oder (C&sub1;-C&sub4;)- Alkyl
sind, und Z und Z' (C&sub1;-C&sub4;)Alkyl sind.
3. Verbindung nach Anspruch 2, worin
R¹ ein verzweigtes (C&sub4;-C&sub7;)Alkyl ist,
R² Methyl, Ethyl, (C&sub1;-C&sub2;)Alkoxyalkyl mit,
unabhängig davon, der angegebenen Anzahl von C-Atomen
in jedem Alkyl-Rest, (C&sub2;-C&sub5;)Alkenyl,
(C&sub2;-C&sub5;)Alkynyl oder Benzyl ist, wo der Phenylring
unsubstituiert oder mit Halogen substituiert ist, und
A und B gleich oder verschieden voneinander
ein unsubstituiertes Naphthyl,
ein unsubstituiertes oder substituiertes Phenyl
mit ein bis drei der gleichen oder verschiedenen
von Halogen, Nitro, Cyano, (C&sub1;-C&sub4;)Alkyl,
Halogen(C&sub1;-C&sub4;)alkyl, Cyano(C&sub1;-C&sub4;)alkyl,
(C&sub1;-C&sub4;)Alkoxy, (C&sub1;-C&sub4;)Alkoxy-
(C&sub1;-C&sub4;)alkyl mit, unabhängig davon, der
angegebenen Anzahl von C-Atomen in jedem
Alkyl-Rest, -COD,
(C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, Thiocyanato, ein
unsubstituiertes oder substituiertes Phenyl mit ein
oder zwei der gleichen oder verschiedenen von
Halogen, Nitro, (C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy,
Carboxy, (C&sub1;-C&sub4;)Alkoxycarbonyl,
(C&sub1;-C&sub4;)Alkanoyloxy, NH&sub2;, NHZ oder NZZ', oder Phenoxy, wo
der Phenyl-Ring unsubstituiert oder mit ein oder zwei
der gleichen oder verschiedenen von Halogen, Nitro,
(C&sub1;-C&sub4;)Alkyl, (C&sub1;-C&sub4;)Alkoxy, Carboxy,
(C&sub1;-C&sub4;)Alkoxycarbonyl, (C&sub1;-C&sub4;)Alkanoyloxy,
NH&sub2;, NHZ, NZZ' substituiert ist, sind,
wo D Wasserstoff oder (C&sub1;-C&sub4;)Alkyl ist, und Z und
Z' (C&sub1;-C&sub4;)Alkyl sind.
4. Verbindung nach Anspruch 3, worin
X und X' 0 sind,
R¹ t-Butyl, Neopentyl(2,2-dimethylpropyl) oder
1,2,2,-Trimethylpropyl ist,
R² Methyl, Methoxymethyl, (C&sub2;-C&sub4;)Alkenyl,
(C&sub2;-C&sub5;)Alkynyl, Benzyl oder 4-Halogenbenzyl ist,
und
A und B gleich oder verschieden voneinander Phenyl oder
ein substituiertes Phenyl sind, wo die
Substituenten ein bis drei der gleichen oder
verschiedenen von Halogen, Nitro, (C&sub1;-C&sub4;)Alkyl,
(C&sub1;-C&sub4;)Alkoxy oder Halogen(C&sub1;-C&sub4;)alkyl
sein können.
5. Verbindung nach Anspruch 4, worin
R¹ t-Butyl ist,
R² (C&sub2;-C&sub5;)Alkynyl ist, und
A und B ein unsubstituiertes oder substituiertes Phenyl
sind, wo die Substituenten ein oder zwei der
gleichen oder verschiedenen von Chlor, Fluor,
Brom, Jod, Methyl, Ethyl, Methoxy oder
Trifluormethyl sein können.
6. Verbindung nach Anspruch 5, worin
X und X' 0 sind,
R¹ t-Butyl ist, und
R² 2-Propynyl ist, und (a)
A 4-Methylphenyl ist, und
B 3-Methylphenyl ist, oder (b)
A Phenyl ist, und
B Phenyl, 2,4-Dichlorphenyl oder 3,4-Dichlorphenyl ist.
7. Insektizides Mittel, umfassend ein landwirtschaftlich
verträgliches Verdünnungsmittel bzw. einen Träger und
eine insektizide Verbindung nach einem der vorhergehenden
Ansprüche.
8. Mittel nach Anspruch 7, enthaltend 0,001 bis 90 Gew.-%,
vorzugsweise 0,01 bis 75 Gew.-% der insektiziden
Verbindung.
9. Mittel nach Anspruch 7 oder 8, jedoch mit
zusatzlich enthaltend ein Emulgierungsmittel (a), wobei
das Mittel in Form eines emulgierbaren Konzentrates
vorliegt, zusätzlich enthaltend ein Dispersionsmittel
(b), wobei das Mittel in Form eines benetzbaren Pulvers
vorliegt, enthaltend einen flüssigen landwirtschaftlich
verträglichen Träger und ein Dispersionsmittel (c),
wobei das Mittel in fließbarer Form vorliegt, in Form
von Staub oder Granulat (d) oder zusätzlich enthaltend
einen Lockstoff (e), wobei das Mittel in Form eines
Köders vorliegt.
10. Verfahren zur Kontrolle von Insekten, bei dem man die
Insekten mit einer Insektizid-wirksamen Menge einer
Insektizid-wirksamen Verbindung nach einem der Ansprüche
1 bis 6, jedoch mit
gegebenenfalls in einem Mittel nach Anspruch 7, 8 oder 9
in Kontakt bringt.
11. Verfahren nach Anspruch 10, worin die
Insektizid-wirksame Verbindung wachsenden Pflanzen oder
einem Bereich, wo Pflanzen wachsen sollen, mit einer
Rate von 10 g bis etwa 10 kg der wirksamen Verbindung
pro Hektar, vorzugsweise 100 g bis 5 kg pro Hektar
verabreicht wird.
12. Verfahren nach Anspruch 10 oder 11 zur Kontrolle von
Insekten der Ordnung Lepidoptera oder Coleoptera.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US85848286A | 1986-05-01 | 1986-05-01 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE3779814D1 DE3779814D1 (de) | 1992-07-23 |
DE3779814T2 true DE3779814T2 (de) | 1993-02-04 |
Family
ID=25328414
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE8787303092T Expired - Fee Related DE3779814T2 (de) | 1986-05-01 | 1987-04-09 | Insektentoetende n-substituierte-n'-substituierte-n,n'-diacylhydrazine. |
Country Status (15)
Country | Link |
---|---|
EP (1) | EP0245950B1 (de) |
JP (1) | JP2576865B2 (de) |
KR (1) | KR940010276B1 (de) |
AR (1) | AR242778A1 (de) |
AT (1) | ATE77200T1 (de) |
AU (1) | AU602516B2 (de) |
BR (1) | BR8701825A (de) |
CA (1) | CA1281716C (de) |
DE (1) | DE3779814T2 (de) |
EG (1) | EG18437A (de) |
ES (1) | ES2042556T3 (de) |
GR (1) | GR3004958T3 (de) |
IL (1) | IL82242A (de) |
TR (1) | TR23901A (de) |
ZA (1) | ZA872519B (de) |
Families Citing this family (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK483586A (da) * | 1985-10-21 | 1987-04-22 | Rohm & Haas | Insecticide n'-substituerede-n,n'-diacylhydraziner |
CA1295618C (en) * | 1986-02-28 | 1992-02-11 | Adam Chi-Tung Hsu | Insecticidal n'-substituted-n-acyl -n'-alkylcarbonylhydrazines |
IE59962B1 (en) * | 1986-09-26 | 1994-05-04 | Rohm & Haas | Five-membered heterocyclic derivatives of n'-substituted-n, n'-diacylhydrazines |
JP2767241B2 (ja) * | 1987-04-15 | 1998-06-18 | ロ−ム アンド ハ−ス コンパニ− | 殺虫性のn−(場合により置換された)−n′−置換−n,n′−ジ置換ヒドラジン |
MY107431A (en) * | 1988-06-15 | 1995-12-30 | Rohm & Haas | Insecticidal n''''substituted-n-alkylcarbonyl-n''''-acylhydra zines and n''''substituted-n-acyl-n''''-alkylcarbonylhydrazines. |
AU637573B2 (en) * | 1988-06-16 | 1993-06-03 | Dow Agrosciences Llc | Hydrazine derivatives for pharmaceutical use |
US4857550A (en) * | 1988-08-29 | 1989-08-15 | American Cyanamid Company | Novel insecticidal dibenzoyl-tert-butylcarbazonitrile compounds and method for the preparation thereof |
EP0398842A1 (de) * | 1989-05-16 | 1990-11-22 | Ciba-Geigy Ag | Hydrazid-derivate |
NZ240155A (en) * | 1990-10-29 | 1992-10-28 | Ishihara Sangyo Kaisha | Heterocyclyl acyl and (hexahydro) indanyl acyl substituted hydrazine derivatives, preparation thereof and pesticidal compositions |
IL100643A (en) * | 1991-01-25 | 1996-10-31 | Nippon Kayaku Kk | History of hydrazine and pesticides containing these histories as an active ingredient |
NZ273244A (en) * | 1993-09-06 | 1997-11-24 | Commw Scient Ind Res Org | Substituted hydrazine derivative insecticidal compositions |
US5523325A (en) * | 1993-09-09 | 1996-06-04 | Jacobson; Richard M. | Amidrazones and their use as pesticides |
US7304161B2 (en) | 2003-02-10 | 2007-12-04 | Intrexon Corporation | Diaclhydrazine ligands for modulating the expression of exogenous genes in mammalian systems via an ecdysone receptor complex |
US7456315B2 (en) | 2003-02-28 | 2008-11-25 | Intrexon Corporation | Bioavailable diacylhydrazine ligands for modulating the expression of exogenous genes via an ecdysone receptor complex |
MX361717B (es) | 2013-03-15 | 2018-12-14 | Intrexon Corp | Diacilhidrazinas que contienen boro. |
WO2016044390A1 (en) | 2014-09-17 | 2016-03-24 | Intrexon Corporation | Boron-containing diacylhydrazine compounds |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1491129A (en) * | 1975-06-04 | 1977-11-09 | Guerbet Sa | Iodo-benzene derivatives and an x-ray contrast medium containing them |
JPS56147066A (en) * | 1980-04-17 | 1981-11-14 | Terumo Corp | Specimen for detection of latent blood |
CA1295618C (en) * | 1986-02-28 | 1992-02-11 | Adam Chi-Tung Hsu | Insecticidal n'-substituted-n-acyl -n'-alkylcarbonylhydrazines |
-
1987
- 1987-02-18 CA CA000529977A patent/CA1281716C/en not_active Expired - Fee Related
- 1987-04-07 KR KR1019870003273A patent/KR940010276B1/ko not_active IP Right Cessation
- 1987-04-08 ZA ZA872519A patent/ZA872519B/xx unknown
- 1987-04-09 ES ES87303092T patent/ES2042556T3/es not_active Expired - Lifetime
- 1987-04-09 AT AT87303092T patent/ATE77200T1/de not_active IP Right Cessation
- 1987-04-09 DE DE8787303092T patent/DE3779814T2/de not_active Expired - Fee Related
- 1987-04-09 EP EP87303092A patent/EP0245950B1/de not_active Expired - Lifetime
- 1987-04-13 AU AU71471/87A patent/AU602516B2/en not_active Ceased
- 1987-04-15 BR BR8701825A patent/BR8701825A/pt not_active IP Right Cessation
- 1987-04-15 EG EG215/87A patent/EG18437A/xx active
- 1987-04-17 IL IL82242A patent/IL82242A/xx not_active IP Right Cessation
- 1987-04-20 JP JP62095486A patent/JP2576865B2/ja not_active Expired - Fee Related
- 1987-04-20 TR TR26587A patent/TR23901A/xx unknown
- 1987-04-20 AR AR87307327A patent/AR242778A1/es active
-
1992
- 1992-06-18 GR GR920401283T patent/GR3004958T3/el unknown
Also Published As
Publication number | Publication date |
---|---|
JP2576865B2 (ja) | 1997-01-29 |
AR242778A1 (es) | 1993-05-31 |
BR8701825A (pt) | 1988-02-09 |
EG18437A (en) | 1992-12-30 |
EP0245950A2 (de) | 1987-11-19 |
IL82242A (en) | 1991-06-30 |
EP0245950A3 (en) | 1989-10-04 |
DE3779814D1 (de) | 1992-07-23 |
AU7147187A (en) | 1987-11-05 |
AU602516B2 (en) | 1990-10-18 |
TR23901A (tr) | 1990-11-01 |
GR3004958T3 (de) | 1993-04-28 |
KR870011079A (ko) | 1987-12-19 |
KR940010276B1 (ko) | 1994-10-22 |
ATE77200T1 (de) | 1992-07-15 |
CA1281716C (en) | 1991-03-19 |
ES2042556T3 (es) | 1993-12-16 |
EP0245950B1 (de) | 1992-06-17 |
IL82242A0 (en) | 1987-10-30 |
ZA872519B (en) | 1988-01-27 |
JPS62263150A (ja) | 1987-11-16 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US4985461A (en) | Insecticidal N'-substituted-N,N'-diacylhydrazines | |
US5225443A (en) | Insecticidal N'-substituted-N'-substituted N,N'-diacylhydrazines | |
JP2509583B2 (ja) | 殺虫性化合物およびそれを含む殺虫組成物 | |
DE3779814T2 (de) | Insektentoetende n-substituierte-n'-substituierte-n,n'-diacylhydrazine. | |
EP0234944B1 (de) | Insektizide N'-substituierte N-Acyl-N'-alkylcarbonylhydrazine | |
JP2618234B2 (ja) | 殺虫性n′−置換−n−アルキルカルボニル−n′−アシルヒドラジン | |
DE68908789T2 (de) | Insectizide N'-substituierte-N-alkylcarbonyl-N'-acylhydrazine und N'-substituierte-N-acyl-N'-alkylcarbonyl hydrazine. | |
EP0253468B1 (de) | Sechsgliedrige heterocyclische Derivate von N'-substituierten N,N'-Diacylhydrazinen | |
EP0286746B1 (de) | Insektizide N-(gegebenenfalls substituierte)-N'-substituierte-N,N'-disubstituierte Hydrazine | |
JP2767241B2 (ja) | 殺虫性のn−(場合により置換された)−n′−置換−n,n′−ジ置換ヒドラジン | |
DE3783111T2 (de) | Fuenfgliedrige heterocyclische derivate von n'-substituierten n,n'-diacylhydrazinen. | |
US5354762A (en) | Six-membered heterocyclic derivatives of N'-substituted N,N'-diacylhydrazines | |
JPS62234055A (ja) | 殺虫活性を有するn′−置換−n−アシル−n′−アルキルカルボニルヒドラジン | |
CA1273633A (en) | Insecticidal n-(optionally substituted)-n'- substituted-n,n'-disubstitutedhydrazines | |
IE59966B1 (en) | Insecticidal n-(optionally substituted)-n'-substituted-n, n'-disubstituted hydrazines |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
8364 | No opposition during term of opposition | ||
8339 | Ceased/non-payment of the annual fee |