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Merck

C55402

4-Chloro-3-methylphenol

99%

Sinónimos:

4-Chloro-m-cresol, PCMC

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Fórmula lineal:
ClC6H3(CH3)OH
Número CAS:
Peso molecular:
142.58
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-431-6
Beilstein/REAXYS Number:
1237629
MDL number:
Assay:
99%
Form:
solid
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Quality Level

assay

99%

form

solid

bp

235 °C (lit.)

mp

63-65 °C (lit.)

SMILES string

Cc1cc(O)ccc1Cl

InChI

1S/C7H7ClO/c1-5-4-6(9)2-3-7(5)8/h2-4,9H,1H3

InChI key

CFKMVGJGLGKFKI-UHFFFAOYSA-N

General description

4-Chloro-3-methylphenol, also known as p-chlorocresol or chloroxylenol, is commonly used as a building block in the synthesis of organic compounds. It can be utilized to synthesize various biologically active compounds, including pharmaceuticals and agrochemicals. (2) Additionally, it serves as a potent disinfectant and antiseptic and is also used as a preservative in medicinal products.

Application

  • Compression of mono-4 chloro, 3-methylphenyl phosphate ester and di-4 chloro, 3-methylphenyl phosphate ester through kinetic study: This study discusses a method using 4-chloro-3-methylphenol and POCl3 taken in a 2:1 ratio, exploring their kinetic behaviors (AR Teli, AA Khan, SH Dar, A Rashid, 2017).
  • Commercially Important Chlorinated Phenols: Reviews the usage of 4-chloro-3-methylphenol among other chlorinated phenols in various industrial applications (K Smith, G El-Hiti).


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Danger

Hazard Classifications

Acute Tox. 4 Oral - Aquatic Acute 1 - Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C - Skin Sens. 1B - STOT SE 3

target_organs

Respiratory system

Clase de almacenamiento

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

wgk

WGK 2

flash_point_f

244.4 °F - closed cup

flash_point_c

118.0 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Faceshields, Gloves



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Synthetic and natural phenols
Tyman et al.
Elsevier's Integrated Review Biochemistry (Second Edition) (1996)
Synthesis and biological evaluation of novel aryloxyacetic acid hydrazide derivatives as anticancer agents
Sevil et al.
Synthetic Communications, 51, 2634-2643 (2021)
Synthesis and insecticidal activity evaluation of virtually screened phenylsulfonamides
Gang et al.
Journal of Agricultural and Food Chemistry, 68, 11665-11671 (2020)