U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

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=C(C=CC=C2)C=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
Comparative developmental toxicity of environmentally relevant oxygenated PAHs.
2013-09-01
(η-Cyclo-penta-dien-yl)[(1,2,3,4,4a,12a-η)-naphtho-[2,3-b][1,4]benzodioxine]iron(II) hexa-fluoridophosphate.
2010-08-21
N-(1,5-Dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazol-4-yl)acetamide-naphthalene-2,3-diol (1/1).
2010-06-26
Bile acid-derived mono- and diketals--synthesis, structural characterization and self-assembling properties.
2010-06-21
Bicyclic compounds repress membrane vesicle production and Pseudomonas quinolone signal synthesis in Pseudomonas aeruginosa.
2010-03
Oxidative modification of citrate synthase by peroxyl radicals and protection with novel antioxidants.
2009-12
Hydrolytic metal with a hydrophobic periphery: titanium(IV) complexes of naphthalene-2,3-diolate and interactions with serum albumin.
2008-09-15
Inhibition of serine beta-lactamases by vanadate-catechol complexes.
2008-09-09
Naphthalene-2,3-diol-imidazole (1/1).
2008-08-13
Degradation of phenanthrene and anthracene by Nocardia otitidiscaviarum strain TSH1, a moderately thermophilic bacterium.
2008-08
Impact of estrogenic compounds on DNA integrity in human spermatozoa: evidence for cross-linking and redox cycling activities.
2008-05-10
Structurally diverse aggregating condensations of Ti(IV) catecholates.
2007-10-29
Which is reactive in alkaline solution, boronate ion or boronic acid? Kinetic evidence for reactive trigonal boronic acid in an alkaline solution.
2007-01-22
Terminal group effects on the fluorescence spectra of europium(III) nitrate complexes with a family of amide-based 2,3-dihydroxynaphthalene derivatives.
2006-09
Synthesis, structure, and characterization of molybdenum(VI) imido complexes with N-salicylidene-2-aminophenol.
2006-07-10
Chemical speciation of iron in seawater by cathodic stripping voltammetry with dihydroxynaphthalene.
2006-01-01
The multidrug efflux regulator TtgV recognizes a wide range of structurally different effectors in solution and complexed with target DNA: evidence from isothermal titration calorimetry.
2005-05-27
(Di-2-pyridylamine-kappa2N,N')(naphthalene-2,3-diolato-kappa2O,O')palladium(II) monohydrate and (di-2-pyridylamine-kappa2N,N')(3-oxidonaphthalene-2-carboxylato-kappa2O,O')palladium(II).
2005-02
Evidence for the existence of PAH-quinone reductase and catechol-O-methyltransferase in Mycobacterium vanbaalenii PYR-1.
2004-12
Assessment of catechol induction and glucuronidation in rat liver microsomes.
2004-12
(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).
2004-04
Enhancing chemi-mechanical transduction in microcantilever chemical sensing by surface modification.
2003-06-13
Enhancement of the ETS-10 titanosilicate activity in the shape-selective photocatalytic degradation of large aromatic molecules by controlled defect production.
2003-02-26
Naphthalene diols: a new class of antioxidants intramolecular hydrogen bonding in catechols, naphthalene diols, and their aryloxyl radicals.
2002-07-26
Nanostructured microcantilevers with functionalized cyclodextrin receptor phases: self-assembled monolayers and vapor-deposited films.
2002-07-01
[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]].
2002-02
Selective nonpeptidic inhibitors of herpes simplex virus type 1 and human cytomegalovirus proteases.
2001-03
Molecular mechanisms controlling the rate and specificity of catechol O-methylation by human soluble catechol O-methyltransferase.
2001-02
Naphthalene degradation and incorporation of naphthalene-derived carbon into biomass by the thermophile Bacillus thermoleovorans.
2000-02
OXIDATIVE METABOLISM OF PHENANTHRENE AND ANTHRACENE BY SOIL PSEUDOMONADS. THE RING-FISSION MECHANISM.
1965-06
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:40:54 GMT 2025
Edited
by admin
on Mon Mar 31 21:40:54 GMT 2025
Record UNII
O9U131030Z
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-8707
Preferred Name English
2,3-NAPHTHALENEDIOL
INCI  
INCI  
Official 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 Mon Mar 31 21:40:54 GMT 2025 , Edited by admin on Mon Mar 31 21:40:54 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-156-7
Created by admin on Mon Mar 31 21:40:54 GMT 2025 , Edited by admin on Mon Mar 31 21:40:54 GMT 2025
PRIMARY
CHEBI
38135
Created by admin on Mon Mar 31 21:40:54 GMT 2025 , Edited by admin on Mon Mar 31 21:40:54 GMT 2025
PRIMARY
PUBCHEM
7091
Created by admin on Mon Mar 31 21:40:54 GMT 2025 , Edited by admin on Mon Mar 31 21:40:54 GMT 2025
PRIMARY
NSC
8707
Created by admin on Mon Mar 31 21:40:54 GMT 2025 , Edited by admin on Mon Mar 31 21:40:54 GMT 2025
PRIMARY
EPA CompTox
DTXSID2043903
Created by admin on Mon Mar 31 21:40:54 GMT 2025 , Edited by admin on Mon Mar 31 21:40:54 GMT 2025
PRIMARY
FDA UNII
O9U131030Z
Created by admin on Mon Mar 31 21:40:54 GMT 2025 , Edited by admin on Mon Mar 31 21:40:54 GMT 2025
PRIMARY