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Details

Stereochemistry ACHIRAL
Molecular Formula C10H8O2
Molecular Weight 160.1693
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 2,3-NAPHTHALENEDIOL

SMILES

OC1=CC2=CC=CC=C2C=C1O

InChI

InChIKey=JRNGUTKWMSBIBF-UHFFFAOYSA-N
InChI=1S/C10H8O2/c11-9-5-7-3-1-2-4-8(7)6-10(9)12/h1-6,11-12H

HIDE SMILES / InChI

Molecular Formula C10H8O2
Molecular Weight 160.1693
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
OXIDATIVE METABOLISM OF PHENANTHRENE AND ANTHRACENE BY SOIL PSEUDOMONADS. THE RING-FISSION MECHANISM.
1965 Jun
[The synthesis, 1H NMR and IR study of [(n-Bu)4N]2[Mo2O5(OC10H6O)2] and [(n-Bu)4N]2[Mo4O10 (OC10H6O)2(OCH3)2]].
2002 Feb
Enhancing chemi-mechanical transduction in microcantilever chemical sensing by surface modification.
2003 Oct-Nov
(2,2'-bipyridine-kappa(2)N,N')(2,3-naphthalenediolato-kappa(2)O,O')palladium(II) and (2,2'-biquinoline-kappa(2)N,N')(2,3-naphthalenediolato-kappa(2)O,O')palladium(II).
2004 Apr
Assessment of catechol induction and glucuronidation in rat liver microsomes.
2004 Dec
Chemical speciation of iron in seawater by cathodic stripping voltammetry with dihydroxynaphthalene.
2006 Jan 1
Structurally diverse aggregating condensations of Ti(IV) catecholates.
2007 Oct 29
Degradation of phenanthrene and anthracene by Nocardia otitidiscaviarum strain TSH1, a moderately thermophilic bacterium.
2008 Aug
Impact of estrogenic compounds on DNA integrity in human spermatozoa: evidence for cross-linking and redox cycling activities.
2008 May 10
Inhibition of serine beta-lactamases by vanadate-catechol complexes.
2008 Sep 9
Bile acid-derived mono- and diketals--synthesis, structural characterization and self-assembling properties.
2010 Jun 21
Bicyclic compounds repress membrane vesicle production and Pseudomonas quinolone signal synthesis in Pseudomonas aeruginosa.
2010 Mar
Comparative developmental toxicity of environmentally relevant oxygenated PAHs.
2013 Sep 1
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 07:14:17 GMT 2023
Edited
by admin
on Sat Dec 16 07:14:17 GMT 2023
Record UNII
O9U131030Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,3-NAPHTHALENEDIOL
INCI  
INCI  
Official Name English
NSC-8707
Code English
2,3-NAPHTHALENEDIOL [INCI]
Common Name English
DIHYDROXYNAPHTHALENE, 2,3-
Systematic Name English
2,3-DIHYDROXYNAPHTHALENE
Systematic Name English
Code System Code Type Description
CAS
92-44-4
Created by admin on Sat Dec 16 07:14:17 GMT 2023 , Edited by admin on Sat Dec 16 07:14:17 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-156-7
Created by admin on Sat Dec 16 07:14:17 GMT 2023 , Edited by admin on Sat Dec 16 07:14:17 GMT 2023
PRIMARY
CHEBI
38135
Created by admin on Sat Dec 16 07:14:17 GMT 2023 , Edited by admin on Sat Dec 16 07:14:17 GMT 2023
PRIMARY
PUBCHEM
7091
Created by admin on Sat Dec 16 07:14:17 GMT 2023 , Edited by admin on Sat Dec 16 07:14:17 GMT 2023
PRIMARY
NSC
8707
Created by admin on Sat Dec 16 07:14:17 GMT 2023 , Edited by admin on Sat Dec 16 07:14:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID2043903
Created by admin on Sat Dec 16 07:14:17 GMT 2023 , Edited by admin on Sat Dec 16 07:14:17 GMT 2023
PRIMARY
FDA UNII
O9U131030Z
Created by admin on Sat Dec 16 07:14:17 GMT 2023 , Edited by admin on Sat Dec 16 07:14:17 GMT 2023
PRIMARY