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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 2-PHENOXYPHENOL

SMILES

OC1=C(OC2=CC=CC=C2)C=CC=C1

InChI

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

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
Effects of protonation state on a tyrosine-histidine bioinspired redox mediator.
2010-11-18
Degradation of triclosan by an integrated nano-bio redox process.
2010-08
Molecular determinants of juvenile hormone action as revealed by 3D QSAR analysis in Drosophila.
2009-06-23
Pyrolysis of permethrin and formation of precursors of polychlorinated dibenzo-p-dioxins and dibenzofurans (PCDD/F) under non-oxidative conditions.
2009-03
A bioinspired construct that mimics the proton coupled electron transfer between P680*+ and the Tyr(Z)-His190 pair of photosystem II.
2008-08-13
Different reaction mechanisms of diphenylether and 4-bromodiphenylether with nitrous acid in the 355 nm laser flash photolysis of mixed aqueous solution.
2008-04
Substituent effects on the vibronic coupling for the phenoxyl/phenol self-exchange reaction.
2008-01-17
Crystal structure of the Helicobacter pylori enoyl-acyl carrier protein reductase in complex with hydroxydiphenyl ether compounds, triclosan and diclosan.
2007-11-15
Calculation of vibronic couplings for phenoxyl/phenol and benzyl/toluene self-exchange reactions: implications for proton-coupled electron transfer mechanisms.
2006-12-27
The environmental-endocrine basis of gynandromorphism (intersex) in a crustacean.
2006-12-05
Gas chromatography and mass spectrometry of methoxylated polybrominated diphenyl ethers (MeO-PBDEs).
2006-06
Inhibition of the bacterial enoyl reductase FabI by triclosan: a structure-reactivity analysis of FabI inhibition by triclosan analogues.
2004-01-29
Juvenile hormone agonists affect the occurrence of male Daphnia.
2003-12
Proton-coupled electron transfer versus hydrogen atom transfer in benzyl/toluene, methoxyl/methanol, and phenoxyl/phenol self-exchange reactions.
2002-09-18
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:54:24 GMT 2025
Edited
by admin
on Mon Mar 31 18:54:24 GMT 2025
Record UNII
KVI8N9886N
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2-PHENOXYPHENOL
Systematic Name English
2-HYDROXYDIPHENYL ETHER
Preferred Name English
PHENOL, 2-PHENOXY-
Systematic Name English
O-PHENOXYPHENOL
Systematic Name English
PHENOXYPHENOL, O-
Systematic Name English
2-HYDROXYPHENYL PHENYL ETHER
Systematic Name English
PHENOL, O-PHENOXY-
Systematic Name English
Code System Code Type Description
FDA UNII
KVI8N9886N
Created by admin on Mon Mar 31 18:54:24 GMT 2025 , Edited by admin on Mon Mar 31 18:54:24 GMT 2025
PRIMARY
CAS
2417-10-9
Created by admin on Mon Mar 31 18:54:24 GMT 2025 , Edited by admin on Mon Mar 31 18:54:24 GMT 2025
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EPA CompTox
DTXSID00178879
Created by admin on Mon Mar 31 18:54:24 GMT 2025 , Edited by admin on Mon Mar 31 18:54:24 GMT 2025
PRIMARY
PUBCHEM
75491
Created by admin on Mon Mar 31 18:54:24 GMT 2025 , Edited by admin on Mon Mar 31 18:54:24 GMT 2025
PRIMARY
CHEBI
39261
Created by admin on Mon Mar 31 18:54:24 GMT 2025 , Edited by admin on Mon Mar 31 18:54:24 GMT 2025
PRIMARY