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Merck
CN

467278

Sigma-Aldrich

N-甲基-邻甲苯胺

≥95%

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别名:
2,N-Dimethylaniline, 2-Methyl-N-methylaniline, N,2-Dimethylaniline, N,2-Dimethylbenzenamine, N,o-Dimethylaniline, N-(2-Methylphenyl)methylamine, N-Methyl-2-methylaniline, N-Methyl-2-methylbenzenamine, N-Methyl-N-(o-tolyl)amine, N-Methyl-o-methylaniline, o,N-Dimethylaniline, Methyl(o-tolyl)amine, NSC 9395
线性分子式:
CH3C6H4NHCH3
CAS号:
分子量:
121.18
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

检测方案

≥95%

bp

177-204 °C/740 mmHg (lit.)

密度

0.981 g/mL at 25 °C (lit.)

SMILES字符串

CNc1ccccc1C

InChI

1S/C8H11N/c1-7-5-3-4-6-8(7)9-2/h3-6,9H,1-2H3

InChI key

GUAWMXYQZKVRCW-UHFFFAOYSA-N

一般描述

N-Methyl-o-toluidine can be synthesized by reacting o-toluidine and benzotriazole.

应用

N-Methyl-o-toluidine may be used in the preparation of 2-substituted N-methylindoles.
Reactant for:
  • Palladium-catalyzed coupling reactions
  • Palladium-catalyzed amination of bromoindazoles

象形图

Skull and crossbonesHealth hazard

警示用语:

Danger

危险分类

Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Acute Tox. 3 Oral - Aquatic Chronic 3 - STOT RE 2

WGK

WGK 3

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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Jaakko Laakia et al.
Talanta, 132, 889-893 (2014-12-06)
Eight selected isomeric amines were ionized using atmospheric pressure chemical ionization and atmospheric pressure photoionization producing a protonated molecule [M+H](+) for each amine. The mobility of these ions was measured by ion mobility spectrometry. The amine compound class was shown
A Practical Synthetic Method for N-Methyl-o-Toluidine.
Katritzky AR and Akutagawa K.
Organic preparations and procedures international, 21(3), 340-341 (1989)
Carbon dioxide: a reagent for the simultaneous protection of nucleophilic centers and the activation of alternative locations to electrophilic attack. XVI, A novel synthetic method for the side-chain functionalization of N-methyl-o-toluidine and for the preparation of 2-substituted N-methylindoles.
Katritzky AR, et al.
Heterocycles, 30(1), 407-414 (1990)

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