528854
4-Chloro-3-methylaniline
98%
Synonym(s):
4-Chloro-m-toluidine
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About This Item
Linear Formula:
ClC6H3(CH3)NH2
CAS Number:
Molecular Weight:
141.60
UNSPSC Code:
12352100
PubChem Substance ID:
MDL number:
Product Name
4-Chloro-3-methylaniline, 98%
InChI
1S/C7H8ClN/c1-5-4-6(9)2-3-7(5)8/h2-4H,9H2,1H3
SMILES string
Cc1cc(N)ccc1Cl
InChI key
HIHCTGNZNHSZPP-UHFFFAOYSA-N
assay
98%
mp
82-86 °C (lit.)
Quality Level
Application
4-Chloro-3-methylaniline may be used to synthesize:
- 4-chloro-3-tolylphosphonic acid
- bis(4-chloro-3-tolyl)phosphinic acid
- 4-chloro-3-methylbenzenesulfonyl chloride
- N-(4-chloro-3-methylphenyl)succinamic acid
General description
4-Chloro-3-methylaniline is halogenated aniline. It undergoes diazotization reaction with fluoroboric acid to afford 4-chloro-3-tolylphosphonic acid and bis(4-chloro-3-tolyl)phosphinic acid.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Problems of Orientation in Arylphosphonic Acids. I. 3-Chloro-4-tolylphosphonic Acid1.
Freedman LD and Doak GO.
The Journal of Organic Chemistry, 30(4), 1263-1265 (1965)
Irreversible enzyme inhibitors. CLXXVIII. Active-site-directed irreversible inhibitors of dihydrofolate reductase derived from 1-(4-benzyloxy-3-chlorophenyl)-4, 6-diamino-1, 2-dihydro-2, 2-dimethyl-s-triazine with a terminal sulfonyl fluoride.
Baker BR and Ashton WT.
Journal of Medicinal Chemistry, 13(6), 1161-1165 (1970)
N-(4-Chloro-3-methylphenyl) succinamic acid.
Chaithanya U, et al.
Acta Crystallographica Section E, Structure Reports Online, 68(7), o2003-o2003 (2012)
Dialkyl Esters of Acylphosphonic Acids1
Berlin K, et al.
The Journal of Organic Chemistry, 30(4), 1265-1267 (1965)
Fourier transform infrared and FT-Raman spectral analysis and ab initio calculations for 4-chloro-2-methylaniline and 4-chloro-3-methylaniline.
Arjunan V and Mohan S.
Journal of Molecular Structure, 892(1), 289-299 (2008)
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