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Details

Stereochemistry ACHIRAL
Molecular Formula C15H16O
Molecular Weight 212.2869
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-CUMYLPHENOL

SMILES

CC(C)(C1=CC=CC=C1)C2=CC=C(O)C=C2

InChI

InChIKey=QBDSZLJBMIMQRS-UHFFFAOYSA-N
InChI=1S/C15H16O/c1-15(2,12-6-4-3-5-7-12)13-8-10-14(16)11-9-13/h3-11,16H,1-2H3

HIDE SMILES / InChI

Molecular Formula C15H16O
Molecular Weight 212.2869
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Are structural analogues to bisphenol a safe alternatives?
2014-05
Bisphenol A and its analogues activate human pregnane X receptor.
2012-03
Rational quantitative structure-activity relationship (RQSAR) screen for PXR and CAR isoform-specific nuclear receptor ligands.
2010-12-05
Dispersive liquid-liquid microextraction versus single-drop microextraction for the determination of several endocrine-disrupting phenols from seawaters.
2010-03-15
Renal Tubular Cyst Formation in Newborn Rats Treated with p-Cumylphenol.
2009-06
ERRgamma tethers strongly bisphenol A and 4-alpha-cumylphenol in an induced-fit manner.
2008-08-29
Micelle-mediated extractions using nonionic surfactant mixtures and HPLC-UV to determine endocrine-disrupting phenols in seawaters.
2008-06
[Status of trace organic pollution in the network water came from Huangpu River].
2008-03
Direct evidence revealing structural elements essential for the high binding ability of bisphenol A to human estrogen-related receptor-gamma.
2008-01
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Comparative susceptibility of newborn and young rats to six industrial chemicals.
2005-12
[Studies on chemical constitutes of green alga Chaetomorpha basiretorsa and their bioactivity].
2005-08
Estrogenic activity of impurities in industrial grade bisphenol A.
2005-05-15
Immature rat uterotrophic assay of 18 chemicals and Hershberger assay of 30 chemicals.
2003-02-01
Male-specific suppression of hepatic microsomal UDP-glucuronosyl transferase activities toward sex hormones in the adult male rat administered bisphenol A.
2002-12-15
Identification of unknown surfactants using electrospray mass spectrometry and NMR spectroscopy preceded by liquid ionization mass spectrometry.
2002-05
Comparison of reporter gene assay and immature rat uterotrophic assay of twenty-three chemicals.
2002-01-15
Measurement of estrogenic activity of chemicals for the development of new dental polymers.
2001-09-22
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:15:17 GMT 2025
Edited
by admin
on Mon Mar 31 19:15:17 GMT 2025
Record UNII
2RLA3OL3QT
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-CUMYLPHENOL
Common Name English
NSC-6237
Preferred Name English
4-(.ALPHA.,.ALPHA.-DIMETHYLBENZYL)PHENOL
Systematic Name English
2-PHENYL-2-(4-HYDROXYPHENYL)PROPANE
Systematic Name English
4-HYDROXYDIPHENYLDIMETHYLMETHANE
Common Name English
PHENOL, 4-(1-METHYL-1-PHENYLETHYL)-
Systematic Name English
PHENYLISOPROPYL)PHENOL, 4-(2-
Common Name English
4-CUMYLPHENOL
Systematic Name English
PHENOL, P-(.ALPHA.,.ALPHA.-DIMETHYLBENZYL)-
Common Name English
4-(1-METHYL-1-PHENYLETHYL)PHENOL
Systematic Name English
4-.ALPHA.-CUMYLPHENOL
Systematic Name English
4-(DIMETHYLPHENYLMETHYL)PHENOL
Systematic Name English
P-(.ALPHA.-CUMYL)PHENOL
Common Name English
2-(4-HYDROXYPHENYL)-2-PHENYLPROPANE
Systematic Name English
P-(.ALPHA.,.ALPHA.-DIMETHYLBENZYL)PHENOL
Common Name English
Code System Code Type Description
HSDB
8089
Created by admin on Mon Mar 31 19:15:17 GMT 2025 , Edited by admin on Mon Mar 31 19:15:17 GMT 2025
PRIMARY
DRUG BANK
DB06902
Created by admin on Mon Mar 31 19:15:17 GMT 2025 , Edited by admin on Mon Mar 31 19:15:17 GMT 2025
PRIMARY
PUBCHEM
11742
Created by admin on Mon Mar 31 19:15:17 GMT 2025 , Edited by admin on Mon Mar 31 19:15:17 GMT 2025
PRIMARY
CAS
599-64-4
Created by admin on Mon Mar 31 19:15:17 GMT 2025 , Edited by admin on Mon Mar 31 19:15:17 GMT 2025
PRIMARY
EPA CompTox
DTXSID3022536
Created by admin on Mon Mar 31 19:15:17 GMT 2025 , Edited by admin on Mon Mar 31 19:15:17 GMT 2025
PRIMARY
NSC
6237
Created by admin on Mon Mar 31 19:15:17 GMT 2025 , Edited by admin on Mon Mar 31 19:15:17 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-968-0
Created by admin on Mon Mar 31 19:15:17 GMT 2025 , Edited by admin on Mon Mar 31 19:15:17 GMT 2025
PRIMARY
FDA UNII
2RLA3OL3QT
Created by admin on Mon Mar 31 19:15:17 GMT 2025 , Edited by admin on Mon Mar 31 19:15:17 GMT 2025
PRIMARY