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About This Item
Linear Formula:
ClC6H4NHCH3
CAS Number:
Molecular Weight:
141.60
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
assay
97%
refractive index
n20/D 1.5840 (lit.)
bp
243-244 °C (lit.)
density
1.156 g/mL at 25 °C (lit.)
functional group
amine
chloro
SMILES string
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
General description
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.[1]
Application
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
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
12 - Non Combustible Liquids
wgk_germany
WGK 3
flash_point_f
>230.0 °F - closed cup
flash_point_c
> 110 °C - closed cup
ppe
Eyeshields, Gloves, type ABEK (EN14387) respirator filter
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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)
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)
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
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