2-[1′,2′,4′-Triazol-3′-yloxymethylene] anilides, their preparation and their use
    63.
    发明授权
    2-[1′,2′,4′-Triazol-3′-yloxymethylene] anilides, their preparation and their use 失效
    2- [1',2',4'-三唑-3'-基氧基亚甲基]酰苯胺,其制备及其用途

    公开(公告)号:US06207692B1

    公开(公告)日:2001-03-27

    申请号:US08765670

    申请日:1997-03-17

    IPC分类号: A01N43653

    摘要: 2-[1′,2′,4′-Triazol-3′-yloxymethylene]anilides of the formula I where the index and the substituents have the following meanings: n is 0, 1, 2, 3, or 4; X is a direct bond, O or NRa; Ra is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl; R1 is nitro, cyano, halogen, unsubstituted or substituted alkyl, alkenyl, alkynyl, alkoxy, alkenyloxy or alkynyloxy; R2 is hydrogen, nitro, cyano, halogen, alkyl, haloalkyl, alkoxy, alkylthio or alkoxycarbonyl; R3 is unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, heteocyclyl, aryl or heteroaryl; R4 is hydrogen, unsubstituted or substituted alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkenyl, alkylcarbonyl or alkoxycarbonyl; R5 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl or cycloalkenyl, processes and intermediates for their preparation and their use are described.

    摘要翻译: 式I的2- [1',2',4'-三唑-3'-基氧基亚甲基]脒,其中指数和取代基具有以下含义:n为0,1,2,3或4; X为 氰基,卤素,未取代或取代的烷基,烯基,炔基,烷氧基,烯氧基或炔氧基; R2是氢,硝基,硝基,环烷基, 氰基,卤素,烷基,卤代烷基,烷氧基,烷硫基或烷氧基羰基; R3是未取代或取代的烷基,烯基,炔基,环烷基,杂环基,芳基或杂芳基; R4是氢,未取代或取代的烷基,烯基,炔基,环烷基,环烯基, 烷基羰基或烷氧基羰基; R5是氢,烷基,烯基,炔基,环烷基或环烯基,它们的制备及其用途的方法和中间体被描述。

    Fungicidal mixtures
    70.
    发明授权

    公开(公告)号:US5587365A

    公开(公告)日:1996-12-24

    申请号:US600822

    申请日:1996-02-13

    CPC分类号: A01N37/50

    摘要: A fungicidal mixture containinga) the oxime ether carboxamide of the formula I ##STR1## and b) an azole derivative II selected from the group of compounds II.1 to II.161-[(2RS,4RS;2RS,4SR)-4-bromo-2-(2,4-dichlorophenyl)tetrahydrofuryl]-1H-1,2,4-triazole (II.1)2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol (II.2)(.+-.)-4-chloro-4-[4-methyl-2-(1H-1,2,4-triazol-1-yl-methyl)-1,3-dioxolan-2-yl]phenyl 4-chlorophenyl ether (II.3)(E)-(R,S)-1-(2,4-dichlorophenyl)-4,4-dimethyl-2-(1H-1,2,4-triazol-1-yl)pent-1-en-3-ol (II.4)(Z)-2-(1H-1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)oxirane (II.5)4-(4-chlorophenyl)-2-phenyl-2-(1H-1,2,4-triazolyl methyl)butyronitrile (II.6)3-(2,4-dichlorophenyl)-6-fluoro-2-(1H-1,2,4-triazol-1-yl)quinazolin-4(3H)-one (II.7)bis(4-fluorophenyl)(methyl)(1H-1,2,4-triazol-1-yl-methyl)silane (II.8)(R,S)-2-(2,4-dichlorophenyl)-1-(1H-1,2,4-triazol-1-yl)-hexan-2-ol (II.9)(1RS,5RS;1RS,5SR)-5-(4-chlorobenzyl)-2,2-dimethyl-1-(1H-1,2,4-triazol-1-ylmethyl)cyclopentanol (II.10)N-propyl-N-[2-(2,4,6-trichlorophenoxy)ethyl]-imidazole-1-carboxamide (II.11)(.+-.)-1-[2-(2,4-dichlorophenyl)-4-propyl-1,3-dioxolan-2-ylmethyl]-1H-1,2,4-triazole (II.12)(R,S)-1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol (II.13)(.+-.)-2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-1-yl) propyl 1,1,2,2-tetrafluoroethyl ether (II.14)(E)-1-[1-[[4-chloro-2-(trifluoromethyl)phenyl]imino]-2-propoxyethyl]-1H-imidazole (II.15) and(RS)-2,4'-difluoro-.alpha.-(1H-1,2,4-triazol-1-yl-methyl)benzhydryl alcohol (II.16)in a synergistically active amount is described.