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Details

Stereochemistry ACHIRAL
Molecular Formula C8H8O2
Molecular Weight 136.1479
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3,4-DIHYDROXYSTYRENE

SMILES

OC1=CC=C(C=C)C=C1O

InChI

InChIKey=FBTSUTGMWBDAAC-UHFFFAOYSA-N
InChI=1S/C8H8O2/c1-2-6-3-4-7(9)8(10)5-6/h2-5,9-10H,1H2

HIDE SMILES / InChI

Molecular Formula C8H8O2
Molecular Weight 136.1479
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Quantitative studies on the influence of the bean roasting parameters and hot water percolation on the concentrations of bitter compounds in coffee brew.
2010-03-24
New urinary metabolites formed from ring-oxidized metabolic intermediates of styrene.
2010-01
Chemistry of secondary polyphenols produced during processing of tea and selected foods.
2009-12-28
Quantitative studies on the formation of phenol/2-furfurylthiol conjugates in coffee beverages toward the understanding of the molecular mechanisms of coffee aroma staling.
2007-05-16
Structure determination and sensory analysis of bitter-tasting 4-vinylcatechol oligomers and their identification in roasted coffee by means of LC-MS/MS.
2007-03-07
Effect of copigments and grape cultivar on the color of red wines fermented after the addition of copigments.
2005-10-19
Characterization of anthocyanins and pyranoanthocyanins from blood orange [Citrus sinensis (L.) Osbeck] juice.
2004-12-01
Occurrence of pyranoanthocyanins in sparkling wines manufactured with red grape varieties.
2004-03-10
Tissue histopathology, clinical chemistry and behaviour of adult Comt-gene-disrupted mice.
2003-07-29
Pathway leading to the formation of anthocyanin-vinylphenol adducts and related pigments in red wines.
2003-06-04
Isolation from a shea cake digester of a tannin-degrading Streptococcus gallolyticus strain that decarboxylates protocatechuic and hydroxycinnamic acids, and emendation of the species.
2002-05
Norepinephrine reuptake is impaired in skeletal muscle of hypertensive rats in vivo.
2001-02
Patents

Patents

Substance Class Chemical
Created
by admin
on Mon Mar 31 19:02:11 GMT 2025
Edited
by admin
on Mon Mar 31 19:02:11 GMT 2025
Record UNII
28C0I29E70
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3,4-DIHYDROXYSTYRENE
Preferred Name English
Code System Code Type Description
FDA UNII
28C0I29E70
Created by admin on Mon Mar 31 19:02:11 GMT 2025 , Edited by admin on Mon Mar 31 19:02:11 GMT 2025
PRIMARY
PUBCHEM
151398
Created by admin on Mon Mar 31 19:02:11 GMT 2025 , Edited by admin on Mon Mar 31 19:02:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID20209275
Created by admin on Mon Mar 31 19:02:11 GMT 2025 , Edited by admin on Mon Mar 31 19:02:11 GMT 2025
PRIMARY
MESH
C042750
Created by admin on Mon Mar 31 19:02:11 GMT 2025 , Edited by admin on Mon Mar 31 19:02:11 GMT 2025
PRIMARY
WIKIPEDIA
3,4-DIHYDROXYSTYRENE
Created by admin on Mon Mar 31 19:02:11 GMT 2025 , Edited by admin on Mon Mar 31 19:02:11 GMT 2025
PRIMARY
CAS
6053-02-7
Created by admin on Mon Mar 31 19:02:11 GMT 2025 , Edited by admin on Mon Mar 31 19:02:11 GMT 2025
PRIMARY