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发明授权
US4237142A Combating fungi with 2-carbamoyloxy-3,3-dimethyl-1-phenoxy-1-(1,2,4-tri azol-1-yl)-1-butanes 失效
将2-氨基甲酰氧基-3,3-二甲基-1-苯氧基-1-（1,2,4-三唑-1-基）-1-丁烷与2-氨基甲酰氧基

Combating fungi with 2-carbamoyloxy-3,3-dimethyl-1-phenoxy-1-(1,2,4-tri azol-1-yl)-1-butanes
摘要：
2-Carbamoyloxy-3,3-dimethyl-1-phenoxy-1-(1,2,4-triazol-1-yl)-1-butanes of the formula ##STR1## in which R is alkyl, halogenoalkyl, alkoxycarbonyl, alkoxyalkyl, substituted phenyl or alkylsulphonyl-alkenyl-carbamoyl,X each independently is halogen, alkyl, cycloalkyl, alkoxy, halogenoalkyl, alkylthio, alkoxycarbonyl, optionally substituted phenyl, optionally substituted phenoxy, optionally substituted phenylalkyl, amino, cyano or nitro, andn is 0, 1, 2, 3, 4 or 5,as the free base, salt or metal salt complex thereof which possess fungicidal properties.
摘要（中）：

具有式“IMAGE”的2-氨基甲酰氧基-3,3-二甲基-1-苯氧基-1-（1,2,4-三唑-1-基）-1-丁烷，其中R是烷基，卤代烷基，烷氧基羰基，烷氧基烷基 取代的苯基或烷基磺酰基 - 烯基 - 氨基甲酰基，X各自独立地为卤素，烷基，环烷基，烷氧基，卤代烷基，烷硫基，烷氧基羰基，任选取代的苯基，任选取代的苯氧基，任选取代的苯基烷基，氨基，氰基或硝基，n为0 ，1,2,3,4或5，作为其具有杀真菌性质的游离碱，其盐或金属盐络合物。

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