N,N'-diaryl-N-alkylureas and method of use
    41.
    发明授权
    N,N'-diaryl-N-alkylureas and method of use 失效
    N,N'-二芳基-N-烷基脲及其使用方法

    公开(公告)号:US4855478A

    公开(公告)日:1989-08-08

    申请号:US128005

    申请日:1987-11-30

    申请人: Frank X. Woolard

    发明人: Frank X. Woolard

    摘要: An N,N-diaryl-N-alkylurea having the formula ##STR1## wherein R.sub.1, R.sub.2, R.sub.3 and R.sub.4 are the same or different and are selected from the group consisting of hydrogen, halogen, cyano, trifluoromethyl, trifluoromethylthio, trifluoromethyl thionyl, trifluoromethane sulfonyl, sulfonamido, substituted phenoxy and substituted pyridyloxy groups wherein the substituent is any one of halogen, cyano, trifluoromethyl, trifluoromethylthio, trifluoromethyl thionyl, trifluoromethane sulfonyl, sulfonamido; andR.sub.5 is selected from the group consisting of alkyl, alkenyl, haloalkyl, haloalkenyl, hydroxyalkyl, hydroxylalkenyl, acetoxyalkyl, acetoxyalkenyl, mercaptoalkyl, and mercaptoalkenyl, wherein the alkyl or alkenyl group in each alkyl- or alkenyl-containing moiety has from 3 to 6 carbon atoms;X is oxygen or sulfur;and agriculturally acceptable salts thereof.Also disclosed is an herbicidal composition and method of treating weeds.

    摘要翻译: 具有式“IMAGE”的N,N-二芳基-N-烷基脲其中R 1,R 2,R 3和R 4相同或不同,并且选自氢,卤素,氰基,三氟甲基,三氟甲硫基,三氟甲基亚硫酰基, 三氟甲磺酰基,亚磺酰氨基,取代的苯氧基和取代的吡啶氧基,其中取代基是卤素,氰基,三氟甲基,三氟甲硫基,三氟甲基亚硫酰基,三氟甲磺酰基,亚磺酰氨基; 并且R 5选自烷基,烯基,卤代烷基,卤代烯基,羟基烷基,羟基烯基,乙酰氧基烷基,乙酰氧基烯基,巯基烷基和巯基烯基,其中每个含烷基或链烯基的部分中的烷基或链烯基具有3至6个 碳原子 X是氧或硫; 及其农业上可接受的盐。 还公开了一种处理杂草的除草组合物和方法。

    Pyridyloxy derivatives and their use as insecticides
    43.
    发明授权
    Pyridyloxy derivatives and their use as insecticides 失效
    吡啶氧基衍生物及其作为杀虫剂的用途

    公开(公告)号:US4714706A

    公开(公告)日:1987-12-22

    申请号:US868716

    申请日:1986-05-30

    摘要: Nitrogen-containing heterocyclic compounds are represented by the formula: ##STR1## wherein R.sub.1 is either one of the following groups: ##STR2## (in which R.sub.4 is a hydrogen atom, a halogen atom or a methyl group and l is an integer of 1 or 2);R.sub.2 is a hydrogen atom or a methyl group;R.sub.3 is an alkyl group, an alkoxy group, an alkenyl group or an alkenyloxy group, all of which may have optionally one or more substituents;A is either one of the following groups: ##STR3## (in which R.sub.5, R.sub.6, R.sub.7, R.sub.8 and R.sub.9 are, the same or different, each a hydrogen atom or a methyl group,R.sub.10 is a hydrogen atom, a halogen atom or a lower alkyl group and m is an integer of 1 to 4); andX is an oxygen atom or a sulfur atom,which is useful as an insecticidal agent.

    摘要翻译: 含氮杂环化合物由下式表示:其中R 1是以下基团之一:其中R 4是氢原子,卤素原子或甲基,和 是1或2的整数); R2是氢原子或甲基; R3是烷基,烷氧基,烯基或烯氧基,其全部可以具有任选的一个或多个取代基; A是以下组之一: + TR (其中R5,R6,R7,R8和R9各自为氢原子或甲基,R10为相同或不同的 氢原子,卤原子或低级烷基,m为1〜4的整数)。 X为氧原子或硫原子,可用作杀虫剂。

    Herbicide compositions
    48.
    发明授权

    公开(公告)号:US4341550A

    公开(公告)日:1982-07-27

    申请号:US55578

    申请日:1979-07-09

    摘要: Herbicidal compositions consisting of an active herbicidal compound and an antidote therefor and the methods of use of the herbicide composition are described herein. The antidote compound corresponds to the formula: ##STR1## wherein R can be selected from the group consisting of haloalkyl; haloalkenyl; alkyl; alkenyl; cycloalkyl; cycloalkylalkyl; halogen; hydrogen; carboalkoxy; N-alkenylcarbamylalkyl; N-alkenylcarbamyl; N-alkyl-N-alkynylcarbamyl; N-alkyl-N-alkynylcarbamylalkyl; N-alkenylcarbamylalkoxyalkyl; N-alkyl-N-alkynylcarbamylalkoxyalkyl; alkynoxy; haloalkoxy; thiocyanatoalkyl; alkenylaminoalkyl; alkylcarboalkyl; cyanoalkyl; cyanatoalkyl; alkenylaminosulfonoalkyl; alkylthioalkyl; haloalkylcarbonyloxyalkyl; alkyoxycarboalkyl; haloalkenylcarbonyloxyalkyl; hydroxyhaloalkyloxyalkyl; hydroxyalkylcarboalkyoxyalkyl; hydroxyalkyl; alkoxysulfonoalkyl; furyl; thienyl; alkyldithiolenyl; thienalkyl; phenyl and substituted phenyl wherein said substituents can be selected from halogen, alkyl, haloalkyl, alkoxy, carbamyl, nitro, carboxylic acids and their salts, haloalkylcarbamyl; phenylalkyl; phenylhaloalkyl; phenylalkenyl; substituted phenylalkenyl wherein said substituents can be selected from halogen, alkyl, alkoxy; halophenoxy; phenylalkoxy; phenylalkylcarboxyalkyl; phenylcycloalkyl; halophenylalkenoxy; halothiophenylalkyl; halophenoxyalkyl; bicycloalkyl; alkenylcarbamylpyridinyl; alkynylcarbamylpyridinyl; dialkenylcarbamylbicycloalkenyl; alkynylcarbamylbicycloalkenyl; R.sub.1 and R.sub.2 can be the same or different and can be selected from the group consisting of alkenyl; haloalkenyl; hydrogen; alkyl; haloalkyl; alkynyl; cyanoalkyl; hydroxyalkyl; hydroxyhaloalkyl; haloalkylcarboxyalkyl; alkylcarboxyalkyl; alkoxycarboxyalkyl; thioalkylcarboxyalkyl; alkoxycarboalkyl; alkylcarbamyloxyalkyl; amino; formyl; haloalkyl-N-alkylamido; haloalkylamido; haloalkylamidoalkyl; haloalkyl-N-alkylamidoalkyl; haloalkylamidoalkenyl; alkylimino; cycloalkyl; alkylcycloalkyl; alkoxyalkyl; alkylsulfonyloxyalkyl; mercaptoalkyl; alkylaminoalkyl; alkyoxycarboalkenyl; haloalkylcarbonyl; alkylcarbonyl; alkenylcarbamyloxyalkyl; cycloalkylcarbamyloxyalkyl; alkoxycarbonyl; haloalkoxycarbonyl; halophenylcarbamyloxyalkyl; cycloalkenyl; phenyl; substituted phenyl wherein said substituents can be selected from alkyl, halogen, haloalkyl, alkoxy, haloalkylamido, phthalamido, hydroxy, alkylcarbamyloxy, alkenylcarbamyloxy, alkylamido, haloalkylamido, alkylcarboalkenyl; phenylsulfonyl; phenylalkyl; substituted phenylalkyl wherein said substituents can be selected from halogen, alkyl, dioxyalkylene, halophenoxyalkylamidoalkyl; alkylthiodiazolyl; piperidylalkyl; thiazolyl; alkylthiazolyl; benzothiazolyl; halobenzothiazolyl; furylalkyl; pyridyl; alkylpyridyl; alkyloxazolyl; tetrahydrofurylalkyl; 3-cyano, 4,5-polyalkylene-thienyl; .alpha.-haloalkylacetamidophenylalkyl; .alpha.-haloalkylacetamidonitrophenylalkyl; .alpha.-haloalkylacetamidohalohenylalkyl; cyanoalkenyl; R.sub.1 and R.sub.2 when taken together can form a structure consisting of piperidinyl; alkylpiperidinyl; alkyltetrahydropyridyl; morpholyl; alkylmorpholyl; azo-bicyclononyl; benzoalkylpyrrolidinyl; oxazolidyl; alkyloxazolidyl; perhydroquinolyl; alkylaminoalkenyl; provided that when R.sub.1 is hydrogen R.sub.2 is other than hydrogen and halophenyl.

    2-Amino thiazoline derivatives
    49.
    发明授权
    2-Amino thiazoline derivatives 失效
    2-氨基噻唑啉衍生物

    公开(公告)号:US4301167A

    公开(公告)日:1981-11-17

    申请号:US116304

    申请日:1979-06-06

    CPC分类号: A61K31/425 C07D277/18

    摘要: 2-amino thiazoline derivative having Formula I: ##STR1## wherein: R represents --R.sub.1 or --CO--R.sub.2, wherein R.sub.1 represents benzyl monosubstituted in the ortho position by lower alkoxy or in the ortho, meta or para position by lower alkyl, trifluoromethyl or halogen, or R.sub.1 represents cycloalkylmethyl; and R.sub.2 represents cycloalkyl, naphthyl, styryl or substituted phenyl; and R.sub.3, R.sub.4, R.sub.5 and R.sub.6, each independently represent hydrogen or lower alkyl.The said 2-amino thiazoline is useful as a medicine in the preparation of pharmaceutical compositions.

    摘要翻译: 具有式I的2-氨基噻唑啉衍生物:其中:R表示-R1或-CO-R2,其中R1表示低级烷氧基在邻位单取代的邻位或邻位,间位或对位的低级 烷基,三氟甲基或卤素,或R 1表示环烷基甲基; 并且R 2表示环烷基,萘基,苯乙烯基或取代的苯基; 和R 3,R 4,R 5和R 6各自独立地表示氢或低级烷基。 所述2-氨基噻唑啉可用作制备药物组合物的药物。