Fungicide mixtures
    41.
    发明授权
    Fungicide mixtures 失效
    杀菌剂混合物

    公开(公告)号:US6114378A

    公开(公告)日:2000-09-05

    申请号:US171522

    申请日:1998-10-21

    CPC分类号: A01N37/52

    摘要: A fungicidal mixture comprisinga) an oxime ether of the formula I ##STR1## where the substituents have the following meaning: X is oxygen or amino (NH);Y is CH or N;Z is oxygen, sulfur, amino (NH) or C.sub.1 -C.sub.4 -alkylamino (N--C.sub.1 -C.sub.4 -alkyl);R' is C.sub.1 -C.sub.6 -alkyl, C.sub.1 -C.sub.6 -haloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.2 -C.sub.6 -haloalkenyl, C.sub.3 -C.sub.6 -alkynyl, C.sub.3 -C.sub.6 -haloalkynyl, C.sub.3 -C.sub.6 -cycloalkylmethyl, or benzyl which may be partially or fully halogenated and/or may carry one to three of the following radicals: cyano, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -haloalkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.1 -C.sub.4 -haloalkoxy and C.sub.1 -C.sub.4 -alkylthio;andb) a dithiocarbamate (II) selected from the group consisting ofmanganese ethylenebis(dithiocarbamate) (zinc complex) (IIa),manganese ethylenebis(dithiocarbamate) (IIb),zinc ammoniate ethylenebis(dithiocarbamate) (IIc) andzinc ethylenebis(dithiocarbamate) (IId) and/orc) 1-(2-cyano-2-methoxyiminoacetyl)-3-ethylurea (III)H.sub.3 CCH.sub.2 --NHCONH--C(CN).dbd.NOCH.sub.3 (III)in a synergistically active amount.

    摘要翻译: PCT No.PCT / EP97 / 02046 Sec。 371日期:1998年10月21日 102(e)1998年10月21日PCT PCT 1997年4月23日PCT公布。 公开号WO97 / 40677 日期1997年11月6日一种杀真菌混合物,其包含a)式I的肟醚,其中取代基具有以下含义:X是氧或氨基(NH); Y是CH或N; Z是氧,硫,氨基(NH)或C 1 -C 4烷基氨基(N-C 1 -C 4 - 烷基); R'是可以是C 1 -C 6 - 烷基,C 1 -C 6 - 卤代烷基,C 3 -C 6 - 烯基,C 2 -C 6 - 卤代烯基,C 3 -C 6 - 炔基,C 3 -C 6 - 卤代炔基,C 3 -C 6环烷基甲基或苄基 部分或完全卤化和/或可以携带一至三个以下基团:氰基,C 1 -C 4 - 烷基,C 1 -C 4卤代烷基,C 1 -C 4 - 烷氧基,C 1 -C 4 - 卤代烷氧基和C 1 -C 4烷硫基; (IIa),亚乙基双(二硫代氨基甲酸)亚乙酯(IIb),亚氨基亚氨基二(二硫代氨基甲酸)亚胺化锌(IIc))和亚乙基双(二硫代氨基甲酸锌)亚乙基双(二亚硫代氨基甲酸酯) )(IId)和/或c)具有协同活性量的1-(2-氰基-2-甲氧基亚氨基乙酰基)-3-乙基脲(III)H3CCH2-NHCONH-C(CN)= NOCH3(III)

    Fungicidal mixtures
    42.
    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.

    Fungicidal compositions
    46.
    发明授权
    Fungicidal compositions 失效
    杀真菌剂

    公开(公告)号:US5317027A

    公开(公告)日:1994-05-31

    申请号:US87317

    申请日:1993-07-08

    CPC分类号: A01N37/50

    摘要: Fungicidal compositions consisting ofa) methyl .alpha.-methoximino-2-[(2-methylphenoxy)-methyl]-phenylacetate ##STR1## and b) an azole active ingredient selected from the following group:(Z)-2-(1,2,4-triazol-1-ylmethyl)-2-(4-fluorophenyl)-3-(2-chlorophenyl)-oxirane of the formula ##STR2## 1-butyl-1-(2,4-dichlorophenyl)-2-(1,2,4-triazol-1-yl)-ethanol (common name hexaconazole), 1-[(2-chlorophenyl)methyl]-1-(1,1-dimethyl)-2- (1,2,4-triazol-1-yl-ethanol, 1-(4-fluorophenyl)- 1-(2-fluorophenyl)-2-(1,2,4-triazol-1-yl)-ethanol (common name flutriafol), (RS)-4-(4-chlorophenyl)-2-phenyl-2 (1H-1,2,4-triazol-1-yl-methyl)-butyronitrile, 1-[(2 RS, 4 RS; 2 RS, 4 SR)-4-bromo-2-(2,4-dichlorophenyl)-tetrahydrofurfuryl]-1H-1,2,4-triazole, 3-(2,4-dichlorophenyl)-2-(1H-1,2,4-triazol-1-yl)-quinazolin-4(3H)-one, (RS)-2,2-dimethyl-3-(2-chlorobenzyl)-4-(1H-1,2,4- triazol-1-yl)-butan-3-ol, bitutanol, triadimefon, triadimenol, cyproconazole, dichlobutrazol, difenoconazole, diniconazole, etaconazole, propiconazole, flusilazole, tebuconazole, imazalil, penconazole, prochloraz, tetraconazole and salts of such azole active ingredients,and methods of combating fungi with such compositions.

    摘要翻译: 由a)甲基α-甲氧基亚氨基-2 - [(2-甲基苯氧基) - 甲基] - 苯基乙酸酯组成的杀真菌组合物和b)选自以下组的唑类活性成分:(Z)-2-(1,2 ,4-三唑-1-基甲基)-2-(4-氟苯基)-3-(2-氯苯基) - 环氧丙烷的方法其中1-(1-(2,4-二氯苯基)-2-( 1,2,4-三唑-1-基) - 乙醇(通用名己唑),1 - [(2-氯苯基)甲基] -1-(1,1-二甲基)-2-(1,2,4-三唑-1-基) 三唑-1-基 - 乙醇,1-(4-氟苯基)-1-(2-氟苯基)-2-(1,2,4-三唑-1-基) - 乙醇(俗名氟替芬),(RS) -4-(4-氯苯基)-2-苯基-2(1H-1,2,4-三唑-1-基 - 甲基) - 丁腈,1 - [(2RS,4RS; 2RS,4RR) -4-溴-2-(2,4-二氯苯基) - 四氢糠基] -1H-1,2,4-三唑,3-(2,4-二氯苯基)-2-(1H-1,2,4-三唑 -1-基) - 喹唑啉-4(3H) - 酮,(RS)-2,2-二甲基-3-(2-氯苄基)-4-(1H-1,2,4-三唑-1-基) 丁苯醇,三唑酮,三唑醇,环丙唑唑,二氯倍唑,苯醚甲环唑,二菌唑,依康唑,丙咪唑 e,氟替唑,戊唑醇,咪达唑仑,康康唑,丙氯灵,噻卡唑和这些唑类活性成分的盐,以及用这种组合物对抗真菌的方法。

    Fungicidal mixtures
    47.
    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
    48.
    发明授权
    Fungicidal mixtures 失效
    杀菌混合物

    公开(公告)号:US5508283A

    公开(公告)日:1996-04-16

    申请号:US305396

    申请日:1994-09-13

    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. -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,Y 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-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,Y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 芳基或环丙基,以协同活性的量描述。

    Fungicidal mixtures
    49.
    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.