540668
5-Chloro-2-methylphenol
97%
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About This Item
Linear Formula:
ClC6H3(CH3)OH
CAS Number:
Molecular Weight:
142.58
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
226-160-3
MDL number:
Assay:
97%
InChI key
KKFPXGXMSBBNJI-UHFFFAOYSA-N
InChI
1S/C7H7ClO/c1-5-2-3-6(8)4-7(5)9/h2-4,9H,1H3
SMILES string
Cc1ccc(Cl)cc1O
assay
97%
mp
72-76 °C (lit.)
functional group
chloro
Quality Level
Related Categories
General description
5-Chloro-2-methylphenol (5-chloro-o-cresol) can be synthesized from 5-chloro-2-methylaniline. 5-Chloro-2-methylphenol is formed as one of the hydroxylation reaction products of p-chlorotoluene.
Application
5-Chloro-2-methylphenol may be used in the synthesis of 4-chlorosalicylaldehyde triacetate and 1-chloro-3-isopropoxy-4-methylbenzene.
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials
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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Hydroxylation of para-chlorotoluene by model complexes of cytochrome P-450.
Sakurai H, et al.
Inorgorganica Chimica Acta, 91(4), 233-236 (1984)
A synthesis of micandrol-C a novel methylthiophenanthrenediol isolated from the trunkwood of Micandropsis scleroxylon.
Sargent MV and Zwicky AB.
Journal of the Chemical Society. Perkin Transactions 1, 6, 1713-1715 (1990)
Coordination in Solutions. II. Acid Dissociation Constants in Water and Structural Reassignments of the Isomeric Chlorosalicylaldehydes1, 2.
Postmus Jr C, et al.
The Journal of Organic Chemistry, 29(9), 233-236 (1984)
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