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Dithiocarboamic acid salts or urea derivs - from urea derivs and dithio-carbamic acid salts, fungicides, microbicides

机译:二硫代氨基甲酸盐或脲衍生物-来自尿素衍生物和二硫代氨基甲酸盐,杀真菌剂,杀微生物剂

摘要

Cpds. of gen. formula (I):- where R and R'= H, methyl or ethyl; R' may also be:- A = alkylene (max 4C); R + R' + N may form a 5-6-membered heterocyclic ring opt. contng. -O and/or -N; B = NH-R", or O-R"; R" = H, alkyl (is not 20C), cycloalkyl (is not 6C) or aryl opt. substd. with lower alkyl, nitro and/or halogen; n = 1 when R' = H, methyl or ethyl; n = 2 when R' = are prepd. by reacting a cpd. (II): or its mineral salts, with a cpd. (III):- or its mineral salts; where R and R"' = H, methyl or ethyl; R"' may also be M = ammonium or alkalimetal; R + R"' + N = as signified for R + R' + N; in the presence of polar solvents pref. at 10-80 degrees C. (I) are esp. active against Phytophtora intestans and Fusicladium dendriticum, and also have microbicidal activity against a wide range of partly pathogenic micro-organisms. They are also active against blue- and green algae.
机译:Cpds。的式(I):-其中R和R’= H,甲基或乙基; R′也可以是:-A =亚烷基(最高4℃); R + R'+ N可以形成5-6元杂环opt。继续-O和/或-N; B = NH-R”或O-R”; R” = H,烷基(不大于20℃),环烷基(不大于6℃)或芳基,优选用低级烷基,硝基和/或卤素取代;当R′= H,甲基或乙基时,n = 1; n当R′=通过使cpd。(II):或其无机盐与cpd。(III):-或其无机盐反应而制备时,= 2;其中R和R″′= H,甲基或乙基; R″′也可以是M =铵或碱金属; R + R″′+ N =对R + R′+ N所表示;在极性溶剂存在下制备。在(10)到10-80摄氏度之间。对肠道疫霉菌和树状镰刀菌具有杀灭活性,并且对多种部分致病性微生物也具有杀微生物活性。它们还对抗蓝藻和绿藻。

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