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Details

Stereochemistry ACHIRAL
Molecular Formula C12H10O2
Molecular Weight 186.2066
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4,4'-BIPHENYLDIOL

SMILES

OC1=CC=C(C=C1)C2=CC=C(O)C=C2

InChI

InChIKey=VCCBEIPGXKNHFW-UHFFFAOYSA-N
InChI=1S/C12H10O2/c13-11-5-1-9(2-6-11)10-3-7-12(14)8-4-10/h1-8,13-14H

HIDE SMILES / InChI

Molecular Formula C12H10O2
Molecular Weight 186.2066
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Bisphenol A binds to Ras proteins and competes with guanine nucleotide exchange: implications for GTPase-selective antagonists.
2013-12-12
Preparation of dummy template imprinted polymers at surface of silica microparticles for the selective extraction of trace bisphenol A from water samples.
2010-07-15
Time-dependent integrity during storage of natural surface water samples for the trace analysis of pharmaceutical products, feminizing hormones and pesticides.
2010-04-19
Antioxidant and cyclooxygenase-2-inhibiting activity of 4,4'-biphenol, 2,2'-biphenol and phenol.
2009-06
Synthesis and drug release properties of poly(ethylene oxide) segmented polysulfone copolymers.
2008-05-08
Directed synthesis of hierarchical nanostructured TiO2 catalysts and their morphology-dependent photocatalysis for phenol degradation.
2008-04-01
Effect of substituents in aromatic amines on the activation energy of epoxy-amine reaction.
2007-06-28
Experimental and theoretical study of the CD spectra and conformational properties of axially chiral 2,2'-, 3,3'-, and 4,4'-biphenol ethers.
2007-05-24
Self-assembly and host-guest chemistry of a 3.5-nm coordination nanotube.
2007-04-02
Ultrafast electron-transfer and solvent adiabaticity effects in viologen charge-transfer complexes.
2006-11-16
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Lignan compounds and 4,4'-dihydroxybiphenyl protect C2C12 cells against damage from oxidative stress.
2006-05-26
Lumped kinetics and acute toxicity of intermediates in the ozonation of phenol in saline media.
2006-02-06
Inhibition of melanogenic activity by 4,4'-dihydroxybiphenyl in melanoma cells.
2006-01
Antialgal, antibacterial and antifungal activity of two metabolites produced and excreted by cyanobacteria during growth.
2006
Hydrogen bonding patterns in the cocrystals of 5-nitrouracil with several donor and acceptor molecules.
2005-12-09
Stimulation of topoisomerase II-mediated DNA cleavage by benzene metabolites.
2005-05-30
Effects of benzene metabolites on DNA cleavage mediated by human topoisomerase II alpha: 1,4-hydroquinone is a topoisomerase II poison.
2005-04
Solvent adiabaticity effects on ultrafast electron transfer in viologen charge transfer complexes.
2005-03-10
4,4'-Dihydroxybiphenyl as a new potent tyrosinase inhibitor.
2005-02
Probing the peripheral anionic site of acetylcholinesterase with quantitative structure activity relationships for inhibition by biphenyl-4-acyoxylate-4'-N-Butylcarbamates.
2005
Photocatalytic one-electron oxidation of biphenyl derivatives strongly coupled with the TiO2 surface.
2004-03-30
Comparative study of the uterotrophic potency of 14 chemicals in a uterotrophic assay and their receptor-binding affinity.
2004-01-15
Effects of the environmental oestrogens bisphenol A, tetrachlorobisphenol A, tetrabromobisphenol A, 4-hydroxybiphenyl and 4,4'-dihydroxybiphenyl on oestrogen receptor binding, cell proliferation and regulation of oestrogen sensitive proteins in the human breast cancer cell line MCF-7.
2003-04
Computational studies on pseudorotaxanes by molecular dynamics and free energy perturbation simulations.
2003-02-21
Phenylphenols, biphenols, bisphenol-A and 4-tert-octylphenol exhibit alpha and beta estrogen activities and antiandrogen activity in reporter cell lines.
2002-07-31
Benzene metabolites antagonize etoposide-stabilized cleavable complexes of DNA topoisomerase IIalpha.
2001-08-01
Inhibition of environmental estrogen-induced proliferation of human breast carcinoma MCF-7 cells by flavonoids.
2001-05
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:30:06 GMT 2025
Edited
by admin
on Mon Mar 31 19:30:06 GMT 2025
Record UNII
R8994A0904
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4,4'-BIPHENYLDIOL
Systematic Name English
DIHYDROXYBIPHENYL
INCI  
INCI  
Preferred Name English
4,4'-BIPHENOL
Systematic Name English
GM-W07
Brand Name English
GM-W06
Brand Name English
4,4'-DIHYDROXY-1,1'-BIPHENYL
Systematic Name English
4,4'-DIHYDROXYBIPHENYL
Systematic Name English
DOD
Brand Name English
BIPHENYL-4,4'-DIOL
Systematic Name English
4,4'-BISPHENOL
Common Name English
4,4'-DIHYDROXYDIPHENYL
Common Name English
NSC-8711
Code English
P,P'-BIPHENOL
Common Name English
(1,1'-BIPHENYL)-4,4'-DIOL
Systematic Name English
Code System Code Type Description
EVMPD
SUB169669
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
PUBCHEM
7112
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
CHEBI
34367
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
WIKIPEDIA
4,4'-Dihydroxybiphenyl
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
FDA UNII
R8994A0904
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-200-5
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
CAS
92-88-6
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
EPA CompTox
DTXSID1029120
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
SMS_ID
100000159489
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
NSC
8711
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY
MESH
C027439
Created by admin on Mon Mar 31 19:30:06 GMT 2025 , Edited by admin on Mon Mar 31 19:30:06 GMT 2025
PRIMARY