产品名称

英文名称：N-(tert-Butoxycarbonyl)-4-bromoaniline

同义词

131818-17-2、tert-Butyl (4-bromophenyl)carbamate、tert-butyl N-(4-bromophenyl)carbamate、N-(tert-Butoxycarbonyl)-4-bromoaniline、tert-butyl 4-bromophenylcarbamate、n-boc-4-bromoaniline、N-BOC 4-bromoaniline、tert-Butyl N-(4-bromophenyl)-carbamate、tert-butyl(4-br

产品性质

CAS编号：131818-17-2

分子式：C11H14BrNO2

分子量：272.14

MDL号：MFCD01006612

PubChem编号：2773608

英文别名：131818-17-2|tert-Butyl (4-bromophenyl)carbamate|tert-butyl N-(4-bromophenyl)carbamate|N-(tert-Butoxycarbonyl)-4-bromoaniline|tert-butyl 4-bromophenylcarbamate|n-boc-4-bromoaniline|N-BOC 4-bromoaniline|tert-Butyl N-(4-bromophenyl)-carbamate|tert-butyl(4-br

规格或纯度：97%

英文名称：N-(tert-Butoxycarbonyl)-4-bromoaniline

储存温度：室温

运输条件：常规运输

产品介绍：N-(tert-Butoxycarbonyl)-4-bromoaniline is an N-(tert-butyloxycarbonyl) [N-BOC] protected 4-bromo aniline. Due to the presence of BOC protection, it serves as an ideal substrate for Suzuki coupling reactions. It affords biaryls via reaction with pyridine or 3-benzaldehyde boronic acids.N-(tert-Butoxycarbonyl)-4-bromoaniline is an N-(tert-butyloxycarbonyl) [N-BOC] protected 4-bromo aniline. Due to the presence of BOC protection, it serves as an ideal substrate for Suzuki coupling reactions. It affords biaryls via reaction with pyridine or 3-benzaldehyde boronic acids.

PubChem SID：488193524

IUPAC Name：tert-butyl N-(4-bromophenyl)carbamate

INCHI：InChI=1S/C11H14BrNO2/c1-11(2,3)15-10(14)13-9-6-4-8(12)5-7-9/h4-7H,1-3H3,(H,13,14)

InChi Key：VLGPDTPSKUUHKR-UHFFFAOYSA-N

Canonical SMILES：CC(C)(C)OC(=O)NC1=CC=C(C=C1)Br

Isomeric SMILES：CC(C)(C)OC(=O)NC1=CC=C(C=C1)Br

WGK Germany：3

PubChem CID：2773608

熔点：103-106 °C

象形图：

信号词：Warning

危险声明：H315 Causes skin irritationH319 Causes serious eye irritationH335 May cause respiratory irritation

预防措施声明：P261,P305+P351+P338,P280,P302+P352,P321,P405,P501,P264,P271,P304+P340,P403+P233,P362+P364,P264+P265,P337+P317,P332+P317,P319

个人防护装备：dust mask type N95 (US)， Eyeshields， Gloves

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