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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=C(C=C1)C=C(O)C=C2

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

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
A light-controlled molecular brake with complete ON-OFF rotation.
2010-03-15
Synthesis, properties, crystal structures, and semiconductor characteristics of naphtho[1,2-b:5,6-b']dithiophene and -diselenophene derivatives.
2010-02-19
New thermal and microbial resistant metal-containing epoxy polymers.
2010
Chromane derivatives of small aromatic molecules: Chemoenzymatic synthesis and growth inhibitory activity on human tumor cell line LoVo WT.
2009-08-15
Experimental and theoretical studies on constitutional isomers of 2,6-dihydroxynaphthalene carbaldehydes. Effects of resonance-assisted hydrogen bonding on the electronic absorption spectra.
2009-01-16
4,4'-(2,6-Dihydroxy-naphthalene-1,5-diyldimethyl-ene)dipyridinium bis-(per-chlorate).
2008-05-30
Toward high-generation rotaxane dendrimers that incorporate a ring component on every branch: noncovalent synthesis of a dendritic [10]pseudorotaxane with 13 molecular components.
2007-06-04
The influence of aromatic residues in hydraphile spacer units: assay by ion selective electrode methods and in bacteria.
2005-05-02
Hydroxynaphthaldehyde phosphate derivatives as potent covalent Schiff base inhibitors of fructose-1,6-bisphosphate aldolase.
2005-04-12
Regiospecific oxidation of naphthalene and fluorene by toluene monooxygenases and engineered toluene 4-monooxygenases of Pseudomonas mendocina KR1.
2005-04-05
Oxidase enzyme immobilisation through electropolymerised films to assemble biosensors for batch and flow injection analysis.
2003-05
Novel solid-state polycondensation I. Oxidative-coupling polymerization of 2,6-dihydroxynaphthalene.
2002-01-21
A covalent vanadium(III) 2-dimensional network and vanadyl chains linked by aryldioxides.
2001-01-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:31:50 GMT 2025
Edited
by admin
on Mon Mar 31 19:31:50 GMT 2025
Record UNII
4XX2ND0257
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,6-NAPHTHOHYDROQUINONE
Common Name English
NSC-62687
Preferred 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
Code System Code Type Description
MESH
C483528
Created by admin on Mon Mar 31 19:31:50 GMT 2025 , Edited by admin on Mon Mar 31 19:31:50 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-465-6
Created by admin on Mon Mar 31 19:31:50 GMT 2025 , Edited by admin on Mon Mar 31 19:31:50 GMT 2025
PRIMARY
CAS
581-43-1
Created by admin on Mon Mar 31 19:31:50 GMT 2025 , Edited by admin on Mon Mar 31 19:31:50 GMT 2025
PRIMARY
EPA CompTox
DTXSID7060384
Created by admin on Mon Mar 31 19:31:50 GMT 2025 , Edited by admin on Mon Mar 31 19:31:50 GMT 2025
PRIMARY
FDA UNII
4XX2ND0257
Created by admin on Mon Mar 31 19:31:50 GMT 2025 , Edited by admin on Mon Mar 31 19:31:50 GMT 2025
PRIMARY
NSC
62687
Created by admin on Mon Mar 31 19:31:50 GMT 2025 , Edited by admin on Mon Mar 31 19:31:50 GMT 2025
PRIMARY
PUBCHEM
93552
Created by admin on Mon Mar 31 19:31:50 GMT 2025 , Edited by admin on Mon Mar 31 19:31:50 GMT 2025
PRIMARY
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