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Merck
CN

479152

Sigma-Aldrich

4-溴苄胺

96%

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About This Item

线性分子式:
BrC6H4CH2NH2
CAS号:
分子量:
186.05
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

方案

96%

沸点

110-112 °C/30 mmHg (lit.)

mp

25 °C (lit.)

密度

1.473 g/mL at 25 °C (lit.)

官能团

amine
bromo

SMILES字符串

NCc1ccc(Br)cc1

InChI

1S/C7H8BrN/c8-7-3-1-6(5-9)2-4-7/h1-4H,5,9H2

InChI key

XRNVSPDQTPVECU-UHFFFAOYSA-N

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一般描述

4-溴苄胺(BBA)又名 p-溴苄胺,是一种芳基溴化物。据报道,在存在红铜的条件下,其可由BBA选择性地形成腈或亚胺。 BBA形成2,6,9-三氮杂双环[3.3.1]壬烷衍生物的formal[4 + 4]反应已有研究。

应用

4-溴苄胺(p-溴苄胺)可用于合成7-[(p-溴苄基)脲基]-7,8-二氢-α-双丁二烯。
它可用于合成以下4-联苯甲胺衍生物:
  • (4′-氟-4-联苯)甲胺
  • (4′-甲氧基-4-联苯)甲胺
  • (2′-甲氧基-4-联苯)甲胺
  • (3′-氰基-4-联苯)甲胺

象形图

Corrosion

警示用语:

Danger

危险声明

危险分类

Skin Corr. 1B

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

>230.0 °F - closed cup

闪点(°C)

> 110 °C - closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Jiaqing Wang et al.
Chemical communications (Cambridge, England), 50(42), 5637-5640 (2014-04-16)
A novel, efficient, convenient and environmentally friendly approach for the synthesis of nitriles and imines from primary amines has been developed. Using commercially available red copper as the catalyst, ammonium bromide as the co-catalyst and molecular oxygen as the sole
Jing Zhuang et al.
Nanoscale, 11(31), 14553-14560 (2019-07-26)
An all-inorganic CsPbI2Br perovskite with excellent phase stability and thermal stability has been considered to be a promising candidate for photovoltaic application. However, low efficiency and high moisture sensitivity hinder its advancement. In this work, we exploit 4-bromobenzylamine hydriodate post-treatment
Silvia Galiano et al.
Bioorganic & medicinal chemistry, 15(11), 3896-3911 (2007-04-05)
We have designed and synthesized two novel series of MCH-R1 antagonists based on a substituted biphenylmethyl urea core. SAR was explored, suggesting that optimal binding with the receptor was achieved when the biphenylmethyl group and the linker were substituted on
Efficient synthesis of 2,6,9-triazabicyclo [3.3.1] nonanes through amine-mediated formal [4+4] reaction of unsaturated imines.
Tanaka K, et al.
Tetrahedron Letters, 53(44), 5899-5902 (2012)
Nitrogenous bisabolene sesquiterpenes from marine invertebrates.
Gulavita NK, et al.
The Journal of Organic Chemistry, 51(26), 5136-5139 (1986)

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