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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 2,6-NAPHTHOHYDROQUINONE

SMILES

OC1=CC2=CC=C(O)C=C2C=C1

InChI

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

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
A covalent vanadium(III) 2-dimensional network and vanadyl chains linked by aryldioxides.
2001 Jan 15
Novel solid-state polycondensation I. Oxidative-coupling polymerization of 2,6-dihydroxynaphthalene.
2002 Jan 21
Oxidase enzyme immobilisation through electropolymerised films to assemble biosensors for batch and flow injection analysis.
2003 May
Hydroxynaphthaldehyde phosphate derivatives as potent covalent Schiff base inhibitors of fructose-1,6-bisphosphate aldolase.
2005 Apr 12
Regiospecific oxidation of naphthalene and fluorene by toluene monooxygenases and engineered toluene 4-monooxygenases of Pseudomonas mendocina KR1.
2005 Apr 5
The influence of aromatic residues in hydraphile spacer units: assay by ion selective electrode methods and in bacteria.
2005 May 2
Toward high-generation rotaxane dendrimers that incorporate a ring component on every branch: noncovalent synthesis of a dendritic [10]pseudorotaxane with 13 molecular components.
2007 Jun 4
4,4'-(2,6-Dihydroxy-naphthalene-1,5-diyldimethyl-ene)dipyridinium bis-(per-chlorate).
2008 May 30
Chromane derivatives of small aromatic molecules: Chemoenzymatic synthesis and growth inhibitory activity on human tumor cell line LoVo WT.
2009 Aug 15
Experimental and theoretical studies on constitutional isomers of 2,6-dihydroxynaphthalene carbaldehydes. Effects of resonance-assisted hydrogen bonding on the electronic absorption spectra.
2009 Jan 16
New thermal and microbial resistant metal-containing epoxy polymers.
2010
Synthesis, properties, crystal structures, and semiconductor characteristics of naphtho[1,2-b:5,6-b']dithiophene and -diselenophene derivatives.
2010 Feb 19
A light-controlled molecular brake with complete ON-OFF rotation.
2010 Mar 15
Patents
Name Type Language
2,6-NAPHTHOHYDROQUINONE
Common Name English
6-HYDROXY-2-NAPHTHOL
Systematic Name English
2,6-NAPHTHALENEDIOL
Systematic Name English
2-HYDROXY-6-NAPHTHOL
Systematic Name English
2,6-DIHYDROXYNAPHTHALINE
Common Name English
2,6-DIHYDROXYNAPHTHALENE
Systematic Name English
NSC-62687
Code English
Code System Code Type Description
MESH
C483528
Created by admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-465-6
Created by admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
PRIMARY
CAS
581-43-1
Created by admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
PRIMARY
EPA CompTox
DTXSID7060384
Created by admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
PRIMARY
FDA UNII
4XX2ND0257
Created by admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
PRIMARY
NSC
62687
Created by admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
PRIMARY
PUBCHEM
93552
Created by admin on Fri Dec 15 19:05:05 GMT 2023 , Edited by admin on Fri Dec 15 19:05:05 GMT 2023
PRIMARY