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吲哚啉-1-羧酸叔丁酯_分子结构_CAS_143262-10-6)
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吲哚啉-1-羧酸叔丁酯

产品号 510149 公司名称 Sigma Aldrich
CAS号 143262-10-6 公司网站 http://www.sigmaaldrich.com
分子式 C13H17NO2 电 话 1-800-521-8956
分子量 219.27958 传 真
纯 度 98% 电子邮件
保 存 Chembase数据库ID: 149852

产品价格信息

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产品别名

标题
tert-Butyl indoline-1-carboxylate
IUPAC标准名
tert-butyl 2,3-dihydro-1H-indole-1-carboxylate
IUPAC传统名
tert-butyl 2,3-dihydroindole-1-carboxylate
别名
N-(tert-Butoxycarbonyl)-2,3-dihydroindole

产品登记号

MDL号 MFCD01318399
PubChem SID 24873481
CAS号 143262-10-6

产品性质

纯度 98%
Empirical Formula (Hill Notation) C13H17NO2
沸点 83-84 °C/0.1 mmHg(lit.)
闪点 110 °C
闪点 230 °F
熔点 46-50 °C(lit.)
GHS危险品标识 GHS07
GHS警示词 Warning
GHS危险声明 H315-H319-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
个人保护装置 dust mask type N95 (US), Eyeshields, Gloves
GHS警示性声明 P261-P305 + P351 + P338
危险公开号 36/37/38
安全公开号 26-36
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
5, 25 g in glass bottle
Application

• Reactant in preparation of aryl alkyl amines via alkylation reactions catalyzed by Pd1
• Reactant in preparation of allyl- and arylindolines2
• Reactant in modular indole synthesis of the highly strained CDEF parent tetracycle of nodulisporic acids A and B3
• Reactant in asymmetric synthesis of β-amino esters via rhodium prolinate complex-catalyzed α-C-H activation / carbenoid insertion reactions4
• Reactant in preparation of substituted indolines and tetrahydroquinolines via cycloaddition approach5
详细说明 (简体中文)
包装
5, 25 g in glass bottle
Application

• Reactant in preparation of aryl alkyl amines via alkylation reactions catalyzed by Pd1
• Reactant in preparation of allyl- and arylindolines2
• Reactant in modular indole synthesis of the highly strained CDEF parent tetracycle of nodulisporic acids A and B3
• Reactant in asymmetric synthesis of β-amino esters via rhodium prolinate complex-catalyzed α-C-H activation / carbenoid insertion reactions4
• Reactant in preparation of substituted indolines and tetrahydroquinolines via cycloaddition approach5

参考文献