Fungicidal mixtures
    102.
    发明授权
    Fungicidal mixtures 失效
    杀菌混合物

    公开(公告)号:US5589479A

    公开(公告)日:1996-12-31

    申请号:US550405

    申请日:1995-10-30

    CPC分类号: A01N43/54

    摘要: A fungicidal synergistic mixture containinga) a compound of the formula I ##STR1## where the substituents have the following meanings: R.sup.1 is a phenyl radical which can carry one to three of the following groups: cyano, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.2 -haloalkyl and C.sub.1 -C.sub.4 -alkoxy, ora pyrimidyl radical which can carry a C.sub.1 -C.sub.3 -alkyl group and/or a phenoxy group, the phenoxy group in turn being able to carry one to three of the following radicals: cyano, halogen, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.2 -haloalkyl and C.sub.1 -C.sub.4 -alkoxy,A is oxygen or oxymethylene (--OCH.sub.2 --);X is CH or N,is oxygen or NR.sup.2, R.sup.2 being hydrogen, C.sub.1 -C.sub.3 -alkyl or C.sub.1 -C.sub.3 -alkoxy, andb) a pyrimidine derivative of the formula II ##STR2## where R is methyl, propyn-1-yl or cyclopropyl, in a synergistically active amount, is described.

    摘要翻译: 一种杀真菌的协同混合物,其含有a)式Ⅰ化合物,其中取代基具有下列含义:R 1是可以携带一至三个下列基团的苯基:氰基,卤素,C 1 -C 4烷基 ,C 1 -C 2卤代烷基和C 1 -C 4 - 烷氧基,或可携带C 1 -C 3 - 烷基和/或苯氧基的嘧啶基,苯氧基依次可携带一至三个下列基团 :氰基,卤素,C 1 -C 4 - 烷基,C 1 -C 2 - 卤代烷基和C 1 -C 4 - 烷氧基,A是氧或甲亚甲基(-OCH 2 - ); X是CH或N,是氧或NR 2,R 2是氢,C 1 -C 3 - 烷基或C 1 -C 3 - 烷氧基,和b)式II的嘧啶衍生物,其中R是甲基,丙炔-1- 或协同活性量的环丙基。

    Fungicidal mixtures
    104.
    发明授权

    公开(公告)号:US5476868A

    公开(公告)日:1995-12-19

    申请号:US311183

    申请日:1994-09-23

    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)tetra-hydrofuryl]-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-l-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.