Dichlorocyclopropylalkyl-hydroxyalkyl azole derivatives
    110.
    发明授权
    Dichlorocyclopropylalkyl-hydroxyalkyl azole derivatives 失效
    二氯环丙基烷基 - 羟基烷基唑衍生物

    公开(公告)号:US4847278A

    公开(公告)日:1989-07-11

    申请号:US864936

    申请日:1986-05-20

    摘要: The novel dichlorocyclopropylalkyl-hydroxyalkyl-azole derivatives of the formula ##STR1## in which R is optionally substituted cycloalkyl or optionally substituted aryl, or is a grouping of the formula ##STR2## wherein X is halogenY is hydrogen or halogen,R.sup.4 and R.sup.5 are identical or different and are alkyl,R.sup.6 is alkyl, halogenoalkyl with more than 2 carbon atoms, alkynyl, alkenyl, optionally substituted cycloalkyl, optionally substituted aryl, optionally substituted aryloxy, optionally substituted arylthio or the groupingR.sup.7 --O--N.dbd.CH--in whichR.sup.7 is alkyl, alkenyl or optionally substituted benzyl, andm is the number 0, 1 or 2,R.sup.1, R.sup.2 and R.sup.3 independently of one another are hydrogen, methyl or chlorine,n is the number 1 or 2 andZ is a nitrogen atom or the CH groupand their acid addition salts and metal salt complexes are very effective as fungicides.

    摘要翻译: 式(Ⅰ)的新型二氯环丙基烷基 - 羟基烷基 - 唑衍生物,其中R是任选取代的环烷基或任选被取代的芳基,或者是下式的组:其中X是卤素Y是氢或卤素,R4 R 5是相同或不同的并且是烷基,R 6是烷基,具有多于2个碳原子的卤代烷基,炔基,烯基,任选取代的环烷基,任选取代的芳基,任选取代的芳氧基,任选取代的芳硫基或基团R 7 -ON = CH- 其中R 7为烷基,烯基或任选取代的苄基,m为0,1或2,R 1,R 2和R 3彼此独立地为氢,甲基或氯,n为数1或2,Z为 氮原子或CH基团及其酸加成盐和金属盐络合物作为杀真菌剂是非常有效的。