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225 条记录 (耗时 0.053 秒)

    Herbicides
    71.
    发明授权
    Herbicides 失效
    除草剂

    公开(公告)号：US4343648A

    公开(公告)日：1982-08-10

    申请号：US251921

    申请日：1981-04-07

    申请人： Gerhard Hamprecht ,  Rolf-Dieter Acker ,  Bruno Wuerzer

    发明人： Gerhard Hamprecht ,  Rolf-Dieter Acker ,  Bruno Wuerzer

    IPC分类号： A01N47/18 ,  A01N43/72 ,  A01N47/20 ,  A01N47/30 ,  A01N47/34 ,  C07C311/63 ,  C07D285/00 ,  C07D285/15

    CPC分类号： C07D285/15 ,  A01N43/72 ,  A01N47/20 ,  A01N47/30 ,  C07C311/63

    摘要： 6H-1,2,4,6-Thiatriazine-1,1-dioxides of the formula ##STR1## where R.sup.1 and R.sup.2 are an aliphatic radical, a cycloaliphatic radical or a substituted aliphatic radical, R.sup.1 may also be unsubstituted or substituted phenyl, unsubstituted or substituted benzyl, or tetrahydrofurylmethyl and R.sup.2 may also be lower alkoxycarbo-lower alkoxy, lower alkylmercapto-carbo-lower alkoxy, lower alkoxy-carbo-lower alkylmercapto, lower alkylmercapto-carbo-lower alkylmercapto, unsubstituted or substituted aryl or unsubstituted or substituted benzyl,R.sup.3 is hydrogen, an aliphatic radical, a cycloaliphatic radical or substituted aliphatic radical,R.sup.4 and R.sup.5 are lower alkyl and R.sup.5 may also be hydrogen,X and Y are oxygen, sulfur, sulfinyl or sulfonyl andX.sup.1 is oxygen or sulfur, and herbicides containing these compounds.

    摘要翻译： 具有下式的其中R 1和R 2是脂族基团，脂环族基团或取代的脂肪族基团的式I-1,2,4,6-三噻嗪-1,1-二氧化物，R 1也可以是未取代的或取代的苯基 ，未取代或取代的苄基或四氢呋喃基甲基，R 2还可以是低级烷氧基羧基 - 低级烷氧基，低级烷基巯基 - 低碳烷基，低级烷氧基 - 低碳烷基巯基，低级烷基巯基 - 低碳烷基巯基，未取代或取代的芳基或未取代的 取代的苄基，R 3是氢，脂族基团，脂环族基团或取代的脂族基团，R 4和R 5是低级烷基，R 5也可以是氢，X和Y是氧，硫，亚磺酰基或磺酰基，X 1是氧或硫， 和含有这些化合物的除草剂。

    Production of .beta.-haloalkylaminosulfonyl halides
    73.
    发明授权
    Production of .beta.-haloalkylaminosulfonyl halides 失效
    制备{62-卤代烷基氨基磺酰卤

    公开(公告)号：US4014931A

    公开(公告)日：1977-03-29

    申请号：US549658

    申请日：1975-02-13

    申请人： Gerhard Hamprecht

    发明人： Gerhard Hamprecht

    IPC分类号： C07C309/80 ,  C07C143/155 ,  C07C143/21

    CPC分类号： C07C309/80

    摘要： The production of .beta.-haloalkylaminosulfonyl halides by the reaction of an aziridine with a sulfuryl halide, and the new .beta.-haloalkylaminosulfonyl halides. The new compounds which can be prepared by the process of the invention are valuable starting materials for the manufacture of plant protection agents, dyes and pharmaceutical substances.

    摘要翻译： 通过氮丙啶与硫酰卤反应生成β-卤代烷基氨基磺酰卤，和新的β-卤代烷基氨基磺酰卤。 可以通过本发明的方法制备的新化合物是用于制备植物保护剂，染料和药物物质的有价值的起始材料。

    Substituted (4-brompyrazole-3-yl) benzazoles
    79.
    发明授权
    Substituted (4-brompyrazole-3-yl) benzazoles 失效

    公开(公告)号：US06482774B1

    公开(公告)日：2002-11-19

    申请号：US09673996

    申请日：2000-10-25

    申请人： Cyrill Zagar ,  Gerhard Hamprecht ,  Markus Menges ,  Olaf Menke ,  Robert Reinhard ,  Peter Schäfer ,  Karl-Otto Westphalen ,  Martina Otten ,  Helmut Walter

    发明人： Cyrill Zagar ,  Gerhard Hamprecht ,  Markus Menges ,  Olaf Menke ,  Robert Reinhard ,  Peter Schäfer ,  Karl-Otto Westphalen ,  Martina Otten ,  Helmut Walter

    IPC分类号： C07D41704

    CPC分类号： C07D413/04 ,  A01N43/74 ,  C07D231/16 ,  C07D417/04 ,  C07D417/14 ,  C07F9/6541 ,  C07F9/65583

    摘要： Substituted (4-bromopyrazol-3-yl)benzazoles I and their salts where R1=H, C1-C4-alkyl, C1-C4-haloalkyl; R2=CN, Cl-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C1-C4-alkylthio, C1-C4-haloalkylthio, C1-C4-alkylsulfinyl, C1-C4-haloalkylsulfinyl, C1-C4-alkylsulfonyl, C1-C4-haloalkylsulfonyl; R4=H, halogen; R5=H, CN, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy or C1-C4-haloalkoxy; Z=—N═C(XR6)—O— or —N═C(XR6)—S—, attached to &agr; via the nitrogen, oxygen or sulfur; X=a chemical bond, oxygen, sulfur, —S(O)—, —SO2—, —NH— or —N(R7)—; R6, R7=Cl-C6-alkyl, Cl-C6-haloalkyl, cyano-Cl-C4-alkyl, hydroxy-C1-C4-alkyl, C3-C6-alkenyl, cyano-C3-C6-alkenyl, C3-C6-haloalkenyl, C3-C6-alkynyl, cyano-C3-C6-alkynyl, C3-C6-haloalkynyl, C1-C4-alkoxy-C1-C4-alkyl, C1-C4-haloalkoxy-C1-C4-alkyl, C3-C4-alkenyloxy-C1-C4-alkyl, C3-C4-alkynyloxy-C1-C4-alkyl, C3-C8-cycloalkyloxy-C1-C4-alkyl, amino-Cl-C4-alkyl, C1-C4-alkylamino-C1-C4-alkyl, di(C1-C4-alkyl)amino-C1-C4-alkyl, Cl-C4-alkylthio-C1-C4-alkyl, C1-C4-haloalkylthio-C1-C4-alkyl, C3-C4-alkenylthio-C1-C4-alkyl, C3-C4-alkynylthio-C1-C4-alkyl, C1-C4-alkylsulfinyl-Cl-C4-alkyl, C1-C4-haloalkylsulfinyl-C1-C4-alkyl, C3-C4-alkenylsulfinyl-C1-C4-alkyl, C3-C4-alkynylsulfinyl-C1-C4-alkyl, C1-C4-alkylsulfonyl-C1-C4-alkyl, C1-C4-haloalkylsulfonyl-C1-C4-alkyl, C3-C4-alkenylsulfonyl-C1-C4-alkyl, C3-C4-alkynylsulfonyl-C1-C4-alkyl, hydroxycarbonyl-C1-C4-alkyl, C1-C4-alkoxycarbonyl-C1-C4-alkyl, which may carry a CN or C1-C4-alkoxycarbonyl group, C1-C4-alkylthiocarbonyl-C1-C4-alkyl, aminocarbonyl-C1-C4-alkyl, C1-C4-alkylaminocarbonyl-C1-C4-alkyl, di(C1-C4-alkyl)aminocarbonyl-C1-C4-alkyl, di(C1-C4-alkyl)-phosphonyl-C1-C4-alkyl, C1-C4-alkoxyimino-C1-C4-alkyl, C3-C4-alkenyloxyimino-C1-C4-alkyl, unsubstituted or substituted C3-C8-cycloalkyl, C3-C8-cycloalkyl-C1-C4-alkyl, phenyl, phenyl-C1-C4-alkyl, 3- to 7-membered heterocyclyl or heterocyclyl-C1-C4-alkyl, where each cycloalkyl and each heterocyclyl ring may contain a CO or CS ring member; if X=a chemical bond, —O—, —S—, —NH— or —N(R7)—, R6 may also be C1-C4-alkylcarbonyl, C1-C4-haloalkylcarbonyl, C1-C4-alkoxycarbonyl, C1-C4-alkylsulfonyl or C1-C4-haloalkylsulfonyl; if X=a chemical bond, R6 may furthermore be CN, SH, NH2, halogen, —CH2—CH(halogen)-R8, —CH═CH—R8 or —CH═C(halogen)-R8, where R8=COOH, C1-C4-alkoxycarbonyl, C1-C4-alkylthiocarbonyl, CONH2, C1-C4-alkylaminocarbonyl, di(C1-C4-alkyl)aminocarbonyl or di(C1-C4-alkyl)phosphonyl; or R6+R7=an unsubstituted or substituted 1,3-propylene, tetramethylene, pentamethylene or ethyleneoxyethylene chain. Use: As herbicides; for the desiccation/defoliation of plants.