物质信息
ID:319999
名称和标识
IUPAC传统名
indole-4-cyano-
IUPAC标准名
1H-indole-4-carbonitrile
别名
Indole-4-carbonitrile4-Cyanoindole4-氰基吲哚
化合物性质
安全信息
个人保护装置
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
欧盟危险性物质标志
有害性 (Xn)德国WGK号
3
GHS危险声明
H302-H315-H317-H318-H335
安全公开号
26-36/37/39
危险公开号
22-37/38-41-43
MSDS下载
GHS警示词
Danger
GHS警示性声明
P261-P280-P305+P351+P338
GHS危险品标识
急性毒性（口服，皮肤接触，吸入），类别4
皮肤刺激，类别2
眼刺激，类别2
皮肤过敏，类别1
特定目标器官毒性 -一次接触，类别3
腐蚀金属，类别1
腐蚀皮肤，类别1A，1B，1C
严重眼损伤，类别1
理化性质
熔点
117-121 °C(lit.)
产品相关信息
纯度
97%
Empirical Formula (Hill Notation)
C9H6N2
描述信息
包装
1, 5 g in glass bottle
Application
Reactant for preparation of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators1Reactant for stereoselective preparation of γ-lactones via prolinol silyl ether catalyzed Friedel-Crafts alkylation reaction2Reactant for iridium-catalyzed borylation reactions3Reactant for parallel synthesis of N-benzylisatin oximes as JNK3 MAP kinase inhibitors4Reactant for preparation of N-aryl indoles5Reactant for preparation of conformationally restricted indole cyclopropylmethylamines as selective serotonin reuptake inhibitors6
1, 5 g in glass bottle
Application
Reactant for preparation of tryptophan dioxygenase inhibitors as potential anticancer immunomodulators1Reactant for stereoselective preparation of γ-lactones via prolinol silyl ether catalyzed Friedel-Crafts alkylation reaction2Reactant for iridium-catalyzed borylation reactions3Reactant for parallel synthesis of N-benzylisatin oximes as JNK3 MAP kinase inhibitors4Reactant for preparation of N-aryl indoles5Reactant for preparation of conformationally restricted indole cyclopropylmethylamines as selective serotonin reuptake inhibitors6
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