Fungicidal N-acyl-S-haloalkyl (or S-halovinyl) thiolcarbamates and
process for preparing same
    7.
    发明授权
    Fungicidal N-acyl-S-haloalkyl (or S-halovinyl) thiolcarbamates and process for preparing same 失效
    杀真菌N-酰基-S-卤代烷基(或S-卤代乙烯基)硫代氨基甲酸酯及其制备方法

    公开(公告)号:US4301174A

    公开(公告)日:1981-11-17

    申请号:US178594

    申请日:1980-08-15

    CPC分类号: A01N47/20 A01N47/12

    摘要: New, highly active fungicides which are N-acyl-S-haloalkyl, or S-halovinyl-thiolcarbamates are prepared by reacting a carboxylic acid, e.g., benzoic acid, with an imidoyl chloride, such as trichloromethylthiomidoyl chloride. These new fungicide thiolcarbamates are effective in fighting a wide range of fungi which attack useful plants, being particularly active against fungi belonging to the different orders Ficomicoeti, Ascomicoeti and Basidiomicoeti.

    摘要翻译: N-酰基-5-卤代烷基或S-卤代乙烯基 - 硫代氨基甲酸酯的新的,高活性的杀真菌剂是通过羧酸如苯甲酸与亚氨基氯例如三氯甲基硫代甲酰氯反应来制备的。 这些新的杀真菌剂硫代氨基甲酸盐有效地对抗广泛的真菌,其攻击有用的植物,对于属于不同种类的Ficomicoeti,Ascomicoeti和Basidiomicoeti的真菌特别有活性。