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2,5-二甲基吲哚_分子结构_CAS_1196-79-8)
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2,5-二甲基吲哚

产品号 D166006 公司名称 Sigma Aldrich
CAS号 1196-79-8 公司网站 http://www.sigmaaldrich.com
分子式 C10H11N 电 话 1-800-521-8956
分子量 145.20104 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 10104

产品价格信息

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产品别名

标题
2,5-Dimethylindole
IUPAC标准名
2,5-dimethyl-1H-indole
IUPAC传统名
1H-indole, 2,5-dimethyl-

产品登记号

MDL号 MFCD00005621
EC号 214-816-1
CAS号 1196-79-8
PubChem SID 24893509

产品性质

Empirical Formula (Hill Notation) C10H11N
纯度 97%
熔点 112-113 °C(lit.)
GHS危险品标识 GHS05
GHS危险品标识 GHS07
GHS警示词 Danger
GHS危险声明 H315-H318-H335
欧盟危险性物质标志 刺激性(Irritant) 刺激性(Irritant) (Xi)
MSDS下载 下载链接
GHS警示性声明 P261-P280-P305 + P351 + P338
危险公开号 37/38-41
安全公开号 26-39
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
1 g in glass bottle
Application

• Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds1
• Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric hydrogenation of unprotected indoles2
• Reactant in enantioselective synthesis of fluorene derivatives via Friedel-Crafts reactions3
• Reactant in preparation of bis-indolyldihydroxybenzoquinones by addition indoles to dichlorobenzoquinone promoted by Bronsted acid4
• Reactant in reaction with hydroxypyrazolines5
详细说明 (简体中文)
包装
1 g in glass bottle
Application

• Reactant in stereoselective preparation of substituted indoles via rhodium-catalyzed enantioselective coupling reaction of indoles with diazo compounds1
• Reactant in stereoselective synthesis of indolines via palladium-catalyzed asymmetric hydrogenation of unprotected indoles2
• Reactant in enantioselective synthesis of fluorene derivatives via Friedel-Crafts reactions3
• Reactant in preparation of bis-indolyldihydroxybenzoquinones by addition indoles to dichlorobenzoquinone promoted by Bronsted acid4
• Reactant in reaction with hydroxypyrazolines5

参考文献