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Details

Stereochemistry ACHIRAL
Molecular Formula C8H10O
Molecular Weight 122.1644
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-ETHYLPHENOL

SMILES

CCC1=CC=CC(O)=C1

InChI

InChIKey=HMNKTRSOROOSPP-UHFFFAOYSA-N
InChI=1S/C8H10O/c1-2-7-4-3-5-8(9)6-7/h3-6,9H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C8H10O
Molecular Weight 122.1644
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Morpho-functional identification of abdominal olfactory receptors in the midge Culicoides imicola.
2010-11
Isolation and characterization of a novel 2-sec-butylphenol-degrading bacterium Pseudomonas sp. strain MS-1.
2010-04
Differences in defensive volatiles of the forked fungus beetle, Bolitotherus cornutus, living on two species of fungus.
2009-11
Modeling quality of premium spanish red wines from gas chromatography-olfactometry data.
2009-08-26
A sex pheromone in the desert tenebrionid beetle Parastizopus armaticeps.
2008-08
Prediction of estrogen receptor agonists and characterization of associated molecular descriptors by statistical learning methods.
2006-11
Data processing and classification analysis of proteomic changes: a case study of oil pollution in the mussel, Mytilus edulis.
2006-09-13
Testing electrostatic complementarity in enzyme catalysis: hydrogen bonding in the ketosteroid isomerase oxyanion hole.
2006-04
Susceptibility of newborn rats to 3-ethylphenol and 4-ethylphenol compared with that of young rats.
2006-03
Structural basis of Src tyrosine kinase inhibition with a new class of potent and selective trisubstituted purine-based compounds.
2006-01
Enrichment of cheeses manufactured from cow's and sheep's milk blends with sheep-like species-related alkylphenols.
2005-03-09
Distribution of conjugates of alkylphenols in milk from different ruminant species.
2005-01
Field studies on efficacy of host odour baits for the biting midge Culicoides impunctatus in Scotland.
2001-06
Genetic polymorphism in the human UGT1A6 (planar phenol) UDP-glucuronosyltransferase: pharmacological implications.
1997-12
A recombinant phenobarbital-inducible rat liver UDP-glucuronosyltransferase (UDP-glucuronosyltransferase 2B1) stably expressed in V79 cells catalyzes the glucuronidation of morphine, phenols, and carboxylic acids.
1994-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:36:53 GMT 2025
Edited
by admin
on Mon Mar 31 19:36:53 GMT 2025
Record UNII
0G9ZK222JX
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-8873
Preferred Name English
3-ETHYLPHENOL
HSDB  
Systematic Name English
3-ETHYLPHENOL [HSDB]
Common Name English
ETHYLPHENOL, 3-
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID0022480
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
PRIMARY
CAS
620-17-7
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
PRIMARY
WIKIPEDIA
3-ETHYLPHENOL
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
PRIMARY
FDA UNII
0G9ZK222JX
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
PRIMARY
MESH
C497701
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
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NSC
8873
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-627-3
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
PRIMARY
HSDB
5720
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
PRIMARY
PUBCHEM
12101
Created by admin on Mon Mar 31 19:36:53 GMT 2025 , Edited by admin on Mon Mar 31 19:36:53 GMT 2025
PRIMARY