物质信息
ID:318261
名称和标识
IUPAC传统名
tert-butyl 5-methoxyindole-1-carboxylate
IUPAC标准名
tert-butyl 5-methoxy-1H-indole-1-carboxylate
别名
N-(tert-Butoxycarbonyl)-5-methoxyindole5-Methoxyindole-1-carboxylic acid tert-butyl esterN-(叔丁氧羰基)-5-甲氧基吲哚N-Boc-5-甲氧基吲哚N-Boc-5-methoxyindole
化合物性质
安全信息
MSDS下载
RID/ADR
UN 2811 6.1/PG 3
欧盟危险性物质标志
有害性 (Xn)德国WGK号
3
GHS危险品标识
急性毒性（口服，皮肤接触，吸入），类别1,2,3
GHS警示词
Danger
联合国危险货物包装类别(PG)
3
联合国危险货物等级
6.1
联合国危险货物编号
2811
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
危险公开号
22-36
GHS危险声明
H301-H319
安全公开号
26
理化性质
熔点
75-79 °C
产品相关信息
Empirical Formula (Hill Notation)
C14H17NO3
纯度
97%
描述信息
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
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
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