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Merck
CN

630918

Sigma-Aldrich

2-溴-N-甲基苯胺

95%

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线性分子式:
BrC6H4NHCH3
CAS号:
分子量:
186.05
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

检测方案

95%

折射率

n20/D 1.6070 (lit.)

bp

107-109 °C/12 mmHg (lit.)

密度

1.589 g/mL at 25 °C (lit.)

SMILES字符串

CNc1ccccc1Br

InChI

1S/C7H8BrN/c1-9-7-5-3-2-4-6(7)8/h2-5,9H,1H3

InChI key

SMVIAQFTVWDWDS-UHFFFAOYSA-N

一般描述

2-Bromo-N-methylaniline can be synthesized via the reduction of 2-bromoformylanilide.

应用

2-Bromo-N-methylaniline can be used to synthesize benzimidazole derivatives, via one pot N-arylation of amides/cyclic amides in the presence of copper iodide nanoparticles. It can also be used in the synthesis of alkyltelluro-substituted aromatic amines, which can show radical trapping ability.

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Acute Tox. 4 Oral

WGK

WGK 2

闪点(°F)

closed cup

闪点(°C)

closed cup

个人防护装备

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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"Nanoparticle mediated organic synthesis (NAMO-synthesis): CuI-NP catalyzed ligand free amidation of aryl halides"
Kumar A and Bishnoi KA
Royal Society of Chemistry Advances, 4(78), 41631- 41635 (2014)
Poon F-J, et al.
Chemistry?A European Journal , 22(36), 12891-12903 (2016)
"Syntheses of 2-Unsubstituted 1H-1, 3-Benzazaphospholes from N-Formyl-2-bromoanilides"
Ghalib M, et al.
Heteroatom Chem., 4(78), 452-459 (2013)

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