5-Substituted-benzoxathiol-2-ones
    13.
    发明授权
    5-Substituted-benzoxathiol-2-ones 失效
    5-取代的苯并恶唑-2-酮

    公开(公告)号:US4349685A

    公开(公告)日:1982-09-14

    申请号:US296761

    申请日:1981-08-27

    申请人: Joseph E. Dunbar

    发明人: Joseph E. Dunbar

    IPC分类号: A01N47/22 C07D327/04

    CPC分类号: C07D327/04 A01N47/22

    摘要: Novel, biologically active, 5-substituted-1,3-benzoxathiol-2-ones are prepared by the reaction of 5-hydroxy-1,3-benzoxathiol-2-one with a substituted isocyanate in the presence of an activating agent and an appropriate organic solvent. The novel compounds are suitable for use as fungicides and as the active constituents in fungicidal compositions.

    摘要翻译: 通过5-羟基-1,3-苯并硫代-2-酮与取代的异氰酸酯在活化剂的存在下反应制备新的生物活性的5-取代-1,3-苯并硫代硫杂-2-酮, 适当的有机溶剂。 新型化合物适用于杀真菌剂和杀真菌剂中的活性成分。

    Aminoalkylthiopyridazine compounds
    16.
    发明授权
    Aminoalkylthiopyridazine compounds 失效
    氨基烷基硫哒嗪化合物

    公开(公告)号:US4058520A

    公开(公告)日:1977-11-15

    申请号:US684224

    申请日:1976-05-07

    IPC分类号: C07D237/18

    CPC分类号: C07D237/18

    摘要: This invention concerns novel aminoalkylthiopyridazine compounds useful for inhibiting the aggregation of blood platelets in animals and a process for preparing the compounds from an isothiuronium salt generated in situ from an aminoalkyl halide and thiourea. The compounds also have fungicidal and nematocidal properties.

    摘要翻译: 本发明涉及用于抑制动物血小板聚集的新型氨基烷基硫代哒嗪化合物,以及由氨基烷基卤化物和硫脲原位产生的异硫脲鎓盐制备化合物的方法。 这些化合物也具有杀真菌和杀线虫的特性。