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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7ClO
Molecular Weight 142.583
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-CHLORO-2-CRESOL

SMILES

CC1=CC(Cl)=CC=C1O

InChI

InChIKey=RHPUJHQBPORFGV-UHFFFAOYSA-N
InChI=1S/C7H7ClO/c1-5-4-6(8)2-3-7(5)9/h2-4,9H,1H3

HIDE SMILES / InChI

Molecular Formula C7H7ClO
Molecular Weight 142.583
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Functional properties of RYR1 mutations identified in Swedish patients with malignant hyperthermia and central core disease.
2010-07
The effect of structure and a secondary carbon source on the microbial degradation of chlorophenoxy acids.
2010-05
Liquid chromatography with post-column reagent addition of ammonia in methanol coupled to negative ion electrospray ionization tandem mass spectrometry for determination of phenoxyacid herbicides and their degradation products in surface water.
2010-02-03
Fulvic acid-mediated phototransformation of mecoprop. A pH-dependent reaction.
2009-07
Pesticide by-products in the Rhône delta (Southern France). The case of 4-chloro-2-methylphenol and of its nitroderivative.
2009-01
Quantitative determination of chlorophenols in leather by pressurized liquid extraction and liquid chromatography with diode-array detection.
2008-01-04
[Simultaneous determination of nine organochlorine pesticide residues in textile by high performance liquid chromatography].
2007-05
Development of a high analytical performance-tyrosinase biosensor based on a composite graphite-Teflon electrode modified with gold nanoparticles.
2006-12-15
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Purification and characterization of two enantioselective alpha-ketoglutarate-dependent dioxygenases, RdpA and SdpA, from Sphingomonas herbicidovorans MH.
2006-07
Photodegradation of chlorinated pesticides dispersed on sand.
2005-03
Enantioselective biodegradation of mecoprop in aerobic and anaerobic microcosms.
2003-11
Study of 202 natural, synthetic, and environmental chemicals for binding to the androgen receptor.
2003-10
Changes in enantiomeric fraction as evidence of natural attenuation of mecoprop in a limestone aquifer.
2003-07
Oxidative transformation of triclosan and chlorophene by manganese oxides.
2003-06-01
Analysis of acidic pesticides using in situ derivatization with alkylchloroformate and solid-phase microextraction (SPME) for GC-MS.
2001-09
Determination of the herbicide 4-chloro-2-methylphenoxyacetic acid and its main metabolite, 4-chloro-2-methylphenol in water and soil by liquid chromatography-electrospray tandem mass spectrometry.
2001-07-20
Structural requirements for voltage-dependent block of muscle sodium channels by phenol derivatives.
2001-04
Phenol derivatives accelerate inactivation kinetics in one inactivation-deficient mutant human skeletal muscle Na(+) channel.
2001-03-23
Determination of chlorophenoxy acid herbicides in water by in situ esterification followed by in-vial liquid-liquid extraction combined with large-volume on-column injection and gas chromatography-mass spectrometry.
2000-04-28
Determination of 2-methyl-4-chlorophenoxy (MCPA) in urine using combined TLC and HPLC methods.
1984-09-01
Effect of phenoxy acids on rat liver regeneration.
1984-02
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:41:41 GMT 2025
Edited
by admin
on Mon Mar 31 18:41:41 GMT 2025
Record UNII
297V63W9RI
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-CHLORO-2-CRESOL
Systematic Name English
4-CHLORO-2-METHYLPHENOL
HSDB  
Preferred Name English
CHLORO-O-CRESOL, 4-
Common Name English
PHENOL, 4-CHLORO-2-METHYL-
Systematic Name English
O-CRESOL, 4-CHLORO-
Common Name English
4-CHLORO-2-METHYLPHENOL [HSDB]
Common Name English
PCOC
Common Name English
4-CHLORO-O-CRESOL
Common Name English
P-CHLORO-O-CRESOL
Common Name English
5-CHLORO-2-HYDROXYTOLUENE
Systematic Name English
NSC-2851
Code English
Classification Tree Code System Code
EPA PESTICIDE CODE 62190
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
Code System Code Type Description
ECHA (EC/EINECS)
216-381-3
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
FDA UNII
297V63W9RI
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
EPA CompTox
DTXSID5022510
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
CAS
1570-64-5
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
HSDB
5841
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
PUBCHEM
14855
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
NSC
2851
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
CHEBI
1800
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
MESH
C019292
Created by admin on Mon Mar 31 18:41:41 GMT 2025 , Edited by admin on Mon Mar 31 18:41:41 GMT 2025
PRIMARY
Related Record Type Details
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