Amino derivatives of tetrasubstituted benzene compounds
    1.
    发明授权
    Amino derivatives of tetrasubstituted benzene compounds 失效
    四取代苯化合物的氨基衍生物

    公开(公告)号:US3871862A

    公开(公告)日:1975-03-18

    申请号:US42175073

    申请日:1973-12-05

    CPC classification number: C07D317/62

    Abstract: WHEREIN R and R'' may be methyl, or a halogen when R'''''' is -CH2-; or R and R'', taken together, may be methylene dioxy; R'''' may be methyl or nitro; R'''''' may be absent or may be -CH2- or -CH ; and X is the residue of a substituted amino or a polyamino radical.

    Antimicrobial 1,2,4,5-tetrasubstituted benzenes having the structure:

    Abstract translation: 具有以下结构的抗微生物剂1,2,4,5-四取代苯:当R“'为-CH 2时,WHEREIN R和R'可以是甲基或卤素; 或R和R'一起可以是亚甲基二氧基; R“可以是甲基或硝基; R“可以不存在或可以是-CH 2 - 或-CH =; 并且X是取代的氨基或聚氨基的残基。

    Amino derivatives of terrasubstituted benzene compounds
    4.
    发明授权
    Amino derivatives of terrasubstituted benzene compounds 失效
    地衣取代苯化合物的氨基衍生物

    公开(公告)号:US3886284A

    公开(公告)日:1975-05-27

    申请号:US36044873

    申请日:1973-05-15

    CPC classification number: A01N33/00 A01N43/30

    Abstract: Antimicrobial 1,2,4,5-tetrasubstituted benzenes having the structure:

    WHEREIN R and R'' may be methyl, or a halogen when R'''''' is -CH2-; or R and R'', taken together, may be methylene dioxy; R'''' may be methyl or nitro; R'''''' may be absent or may be -CH2- or -CH ; and X is the residue of a substituted amino or a polyamino radical.

    Abstract translation: 具有以下结构的抗菌剂1,2,4,5-四取代苯:

    10.
    发明专利
    未知

    公开(公告)号:DE2547774A1

    公开(公告)日:1976-05-20

    申请号:DE2547774

    申请日:1975-10-24

    Abstract: Anti-microbial polymeric quaternary ammonium compounds having linear chains which terminate in quaternary ammonium moieties, such compounds being formed by polymerization which is carried out in such a manner that the linear chains thereof are terminated in random fashion, the reaction resulting in the formation of the compounds being a one-step reaction between 1,4-dihalo-2-butene and a mixture of a difunctional tertiary amine and a monofunctional tertiary amine wherein the molar quantity of the difunctional amine is greater than the molar quantity of the monofunctional amine.

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