Herbicidal 3-(3,4,5,6-tetrahydrophthalimido)-cinnamic esters
    111.
    发明授权
    Herbicidal 3-(3,4,5,6-tetrahydrophthalimido)-cinnamic esters 失效
    除草剂3-(3,4,5,6-四氢邻苯二甲酰亚胺基) - 肉桂酯

    公开(公告)号:US5296452A

    公开(公告)日:1994-03-22

    申请号:US525035

    申请日:1990-05-18

    CPC分类号: C07D209/48 A01N37/46

    摘要: 3-(N-3,4,5,6-Tetrahydrophthalimido)-cinnamic esters of the general formula I ##STR1## where n is 1 or 2 and the substituents have the following meanings:R.sup.1 is hydrogen or fluorine,R.sup.2 is halogen,R.sup.3 is hydrogen, halogen or C.sub.1 -C.sub.4 -alkyl,R.sup.4 is hydrogen, substituted or unsubstituted C.sub.1 -C.sub.6 -alkyl, C.sub.3 -C.sub.7 -cycloalkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkynyl or benzyl,R is C.sub.1 -C.sub.4 -alkyl,processes for their manufacture, and herbicidal agents containing them.

    摘要翻译: 3-(N-3,4,5,6-四氢邻苯二甲酰亚氨基) - 肉桂酸酯,其中n为1或2,并且取代基具有以下含义:R 1为氢或氟,R 2为卤素 R3是氢,卤素或C1-C4-烷基,R4是氢,取代或未取代的C1-C6-烷基,C3-C7-环烷基,C3-C6-烯基,C3-C6-炔基或苄基,R是C1- C4烷基,其制备方法和含有它们的除草剂。

    Carboxylic acid derivatives
    113.
    发明授权
    Carboxylic acid derivatives 失效
    羧酸衍生物

    公开(公告)号:US5085685A

    公开(公告)日:1992-02-04

    申请号:US566536

    申请日:1990-08-13

    摘要: Carboxylic acid derivatives of the general formula I ##STR1## where R.sup.1 and R.sup.2 are each 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/or C.sub.1 -C.sub.4 -alkylthio;R.sup.3 is hydrogen, hydroxyl, cyano, nitro, formyl, halogen, unsubstituted or substituted amino, C.sub.1 -C.sub.4 -alkyl, C.sub.1 -C.sub.4 -alkoxy, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.6 -alkenyloxy, C.sub.3 -C.sub.6 -alkynyl or C.sub.3 -C.sub.6 -alkynyloxy;R.sup.4 is hydrogen or C.sub.1 -C.sub.4 -alkyl;R.sup.5 is unsubstituted or substituted five-membered hetaryl or isoxazolinyl or --CR.sup.6 .dbd.NOR.sup.7 ;R.sup.6 is hydrogen or unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, C.sub.3 -C.sub.8 -cycloalkyl or phenyl;R.sup.7 is unsubstituted or substituted C.sub.1 -C.sub.4 -alkyl, C.sub.3 -C.sub.6 -alkenyl, C.sub.3 -C.sub.8 -cycloalkyl or phenyl;A is oxygen or sulfur;X is nitrogen or methine .dbd.CR.sup.8 --;R.sup.8 is one of the radicals R.sup.3, or R.sup.8 and R.sup.3 together form unsubstituted or substituted 1,3-butadiene-1,4-yl or aza-1,3-butadiene-1,4-yl, andY and Z are each nitrogen or methine .dbd.CH--, their preparation and agents containing them.

    摘要翻译: 其中R 1和R 2各自为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/或C 1 -C 4 - 烷硫基的通式I的羧酸衍生物; R3是氢,羟基,氰基,硝基,甲酰基,卤素,未取代或取代的氨基,C1-C4-烷基,C1-C4-烷氧基,C3-C6-烯基,C3-C6-烯氧基,C3-C6-炔基或C3 -C 6 - 炔氧基; R4是氢或C1-C4-烷基; R5是未取代的或取代的五元杂芳基或异恶唑啉基或-CR 6 = NOR 7; R6是氢或未取代或取代的C1-C4-烷基,C3-C8-环烷基或苯基; R 7为未取代或取代的C 1 -C 4 - 烷基,C 3 -C 6 - 烯基,C 3 -C 8 - 环烷基或苯基; A是氧或硫; X是氮或次甲基= CR8-; R8是基团R3之一,或R8和R3一起形成未取代或取代的1,3-丁二烯-1,4-基或氮杂-1,3-丁二烯-1,4-基,Y和Z各自为氮 或次甲基= CH-,它们的制备物和含有它们的试剂。

    Phenylalkenylcarboxylic acids and their esters
    114.
    发明授权
    Phenylalkenylcarboxylic acids and their esters 失效
    苯基链烯基羧酸及其酯

    公开(公告)号:US4933001A

    公开(公告)日:1990-06-12

    申请号:US217563

    申请日:1988-07-11

    CPC分类号: C07D209/48 A01N37/32

    摘要: Phenylalkenylcarboxylic acid and esters thereof of the general formula I ##STR1## where X is hydrogen or fluorine, R.sup.1 is hydrogen, C.sub.1 C.sub.6 -alkyl, C.sub.5 - or C.sub.6 -cycloalkyl, (C.sub.1 -C.sub.4 -alkoxy)-C.sub.2 -C.sub.4 -alkyl or (C.sub.1 -C.sub.4 -alkylthio)-C.sub.2 -C.sub.4 -alkyl; W is a divalent radical --CH.dbd.CR.sup.2 --; --CH.dbd.CY--; --CH.dbd.CR.sup.2 --CH.sub.2 --; --CH.dbd.CR.sup.2 --CH.dbd.CR.sup.3 -- or ##STR2## where Y is chlorine or bromine and R.sup.2 and R.sup.3 are each hydrogen or C.sub.1 -C.sub.4 -alkyl, with the proviso that X is not F when W is --CH.dbd.CR.sup.2 --, their manufacture, and their use as herbicides.

    摘要翻译: 苯基链烯基羧酸及其通式I的酯其中X是氢或氟,R 1是氢,C 1 -C 6 - 烷基,C 5 - 或C 6 - 环烷基,(C 1 -C 4 - 烷氧基)-C 2 -C 4烷基或 (C 1 -C 4 - 烷硫基)-C 2 -C 4 - 烷基; W是二价基团-CH = CR2-; -CH = CY-; -CH = CR 2 -CH 2 - ; -CH = CR2-CH = CR3-或其中Y是氯或溴,R2和R3各自是氢或C1-C4-烷基,条件是当W是-CH = CR2-时,X不是F, 它们的制造及其作为除草剂的用途。

    Herbicidal agents based on acetanilides

    公开(公告)号:US4373945A

    公开(公告)日:1983-02-15

    申请号:US209961

    申请日:1980-11-24

    摘要: Herbicidal agents containing an N-azolylmethylhaloacetanilide of the formula ##STR1## where R denotes hydrogen or linear or branched alkyl or alkoxy of a maximum of 5 carbon atoms, R.sup.1 denotes hydrogen, halogen, or linear or branched alkyl or alkoxy of a maximum of 5 carbon atoms, R.sup.2 denotes hydrogen, halogen, or linear or branched alkyl or alkoxy of a maximum of 5 carbon atoms, R together with R.sup.2 forms an alkylene chain of a maximum of 6 carbon atoms which is linked in the o-position and is unsubstituted or substituted by linear alkyl of a maximum of 4 carbon atoms, X denotes chlorine or bromine, and A denotes an azole which is attached via a ring nitrogen atom and is unsubstituted or mono- or poly-substituted by halogen, phenyl, alkyl, alkoxy, alkylthio or perfluoroalkyl, each of a maximum of 4 carbon atoms, cyano, carboxy, carbalkoxy of a maximum of 4 carbon atoms in the alkoxy, or alkanoyl of a maximum of 4 carbon atoms, A also denoting a salt of an azole containing 2 or 3 nitrogen atoms, and a haloacetanilide of the formula ##STR2## where R denotes linear or branched alkyl, alkenyl or alkynyl, each of a maximum of 4 carbon atoms, or --A--R.sup.1, A denoting alkylene of 1 or 2 carbon atoms which may be monosubstituted by ethyl or mono- or disubstituted by methyl, and R.sup.1 denoting linear or branched alkoxy, haloalkoxy, alkenoxy, alkynoxy or alkoxyalkoxy, each of a maximum of 4 carbon atoms, cycloalkoxy or cycloalkylmethoxy with 3 to 6 carbon atoms in the cycloalkyl ring, 1,3-dioxolan-2-yl or alkoxycarbonyl of a maximum of 4 carbon atoms in the alkoxy, X denotes chlorine or bromine, and Y.sup.1 and Y.sup.2 are identical or different and each denotes hydrogen or linear or branched alkyl of a maximum of 4 carbon atoms, Y.sup.1 and Y.sup.2 only denoting hydrogen when R is linear or branched alkyl, alkenyl or alkynyl, each of a maximum of 4 carbon atoms.The ratio of N-azolylmethylhaloacetanilide of the formula I to haloacetanilide of the formula II is from 1:0.5 to 1:20 parts by weight.