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Merck
CN

532215

Sigma-Aldrich

N-甲基-3-氯苯胺

97%

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线性分子式:
ClC6H4NHCH3
CAS号:
分子量:
141.60
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

检测方案

97%

折射率

n20/D 1.5840 (lit.)

bp

243-244 °C (lit.)

密度

1.156 g/mL at 25 °C (lit.)

SMILES字符串

CNc1cccc(Cl)c1

InChI

1S/C7H8ClN/c1-9-7-4-2-3-6(8)5-7/h2-5,9H,1H3

InChI key

WFGYSQDPURFIFL-UHFFFAOYSA-N

一般描述

N-Methyl-3-chloroaniline, also known as 3-chloro-N-methylaniline, is a secondary amine. It can undergo C3 borylation in the presence of an iridium catalyst.

应用

N-Methyl-3-chloroaniline may be used as a starting material in the preparation of:2
  • N

  • -(2-bromoethyl)-N-methyl-3-chloroaniline
  • 2-[2-(N-methyl-3-chloroanilino)ethyl]-1,3-isoindolinedione
  • N1-(3-chlorophenyl)-N1-methyl-1,2-ethanediamine dihydrochloride

象形图

Exclamation mark

警示用语:

Warning

危险声明

危险分类

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

WGK

WGK 3

闪点(°F)

>230.0 °F

闪点(°C)

> 110 °C

个人防护装备

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

法规信息

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A Traceless Directing Group for C-H Borylation.
Preshlock SM
Angewandte Chemie (Weinheim an der Bergstrasse, Germany), 125(49), 13153-13157 (2013)
M Giannangeli et al.
Journal of medicinal chemistry, 42(3), 336-345 (1999-02-13)
A series of triazolopyridine derivatives (compounds 2a-l) were synthesized in order to explore the effect of modifications of the alkylpiperazine moiety of trazodone (fragment A) on binding affinity for 5HT2A and alpha1 receptors. All of the synthesized compounds show a
Effect of modifications of the alkylpiperazine moiety of trazodone on 5HT2A and alpha1 receptor binding affinity.
Giannangeli, M
Medicinal Chemistry, 42 (3), 336-345 (1999)

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