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N-Boc-5-甲氧基吲哚_分子结构_CAS_99275-47-5)
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N-Boc-5-甲氧基吲哚

产品号 680613 公司名称 Sigma Aldrich
CAS号 99275-47-5 公司网站 http://www.sigmaaldrich.com
分子式 C14H17NO3 电 话 1-800-521-8956
分子量 247.28968 传 真
纯 度 97% 电子邮件
保 存 Chembase数据库ID: 87802

产品价格信息

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产品别名

标题
N-Boc-5-methoxyindole
IUPAC标准名
tert-butyl 5-methoxy-1H-indole-1-carboxylate
IUPAC传统名
tert-butyl 5-methoxyindole-1-carboxylate
别名
N-(叔丁氧羰基)-5-甲氧基吲哚
N-(tert-Butoxycarbonyl)-5-methoxyindole
5-Methoxyindole-1-carboxylic acid tert-butyl ester

产品登记号

MDL号 MFCD08272248
CAS号 99275-47-5
PubChem SID 24885580

产品性质

Empirical Formula (Hill Notation) C14H17NO3
纯度 97%
熔点 75-79 °C
GHS危险品标识 GHS06
GHS警示词 Danger
GHS危险声明 H301-H319
欧盟危险性物质标志 有害性(Harmful) 有害性(Harmful) (Xn)
MSDS下载 下载链接
个人保护装置 dust mask type N95 (US), Eyeshields, Faceshields, Gloves
GHS警示性声明 P301 + P310-P305 + P351 + P338
RID/ADR UN 2811 6.1/PG 3
危险公开号 22-36
安全公开号 26
联合国危险货物等级 6.1
联合国危险货物编号 2811
联合国危险货物包装类别(PG) 3
德国WGK号 3

产品详细信息

详细说明 (English)
Packaging
1, 10 g in glass bottle
Application
Reactant for preparation of:
• Asymmetric intramolecular Friedel-Crafts alkylation reaction1
• Palladium-catalyzed carboaminoxylations with arylboronic acids and TEMPO catalyst2
• Fluorescent pyrimidopyrimidoindole nucleosides via Suzuki-Miyaura coupling reaction3
• Novel conformationally restricted β- and γ-amino acids4
• 2-(Indolyl) borates, silanes, and silanols5
• DNA minor groove alkylating agents as stable amine-based prodrugs designed for tumor-specific release6
详细说明 (简体中文)
包装
1, 10 g in glass bottle
Application
Reactant for preparation of:
• Asymmetric intramolecular Friedel-Crafts alkylation reaction1
• Palladium-catalyzed carboaminoxylations with arylboronic acids and TEMPO catalyst2
• Fluorescent pyrimidopyrimidoindole nucleosides via Suzuki-Miyaura coupling reaction3
• Novel conformationally restricted β- and γ-amino acids4
• 2-(Indolyl) borates, silanes, and silanols5
• DNA minor groove alkylating agents as stable amine-based prodrugs designed for tumor-specific release6

参考文献