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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 2,7-NAPHTHALENEDIOL

SMILES

OC1=CC2=C(C=C1)C=CC(O)=C2

InChI

InChIKey=DFQICHCWIIJABH-UHFFFAOYSA-N
InChI=1S/C10H8O2/c11-9-3-1-7-2-4-10(12)6-8(7)5-9/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
Covalent titanium aryldioxy one-, two-, and three-dimensional networks and their examination as Ziegler-Natta catalysts.
2001 Apr 23
X-ray structure of beta-cyclodextrin-2,7-dihydroxy-naphthalene.4.6 H(2)O: an unusually distorted macrocycle.
2001 Jul 12
Selective nonpeptidic inhibitors of herpes simplex virus type 1 and human cytomegalovirus proteases.
2001 Mar
Synthesis of 3,5- and 3,6-linked calix[n]naphthalenes.
2002 Feb 8
UV-vis, IR and 1H NMR spectroscopic studies of some mono- and bis-azo-compounds based on 2,7-dihydroxynaphthalene and aniline derivatives.
2005 Dec
Mechanism of cytotoxicity of catechols and a naphthalenediol in PC12-AC cells: the connection between extracellular autoxidation and molecular electronic structure.
2005 Feb 1
Structural basis for the promiscuous biosynthetic prenylation of aromatic natural products.
2005 Jun 16
Naphthalene-2,3-diol-imidazole (1/1).
2008 Aug 13
A new route to obtain high-yield multiple-shaped gold nanoparticles in aqueous solution using microwave irradiation.
2008 Jul 21
Influence of the polymer backbone structure on the properties of aromatic ionomers with pendant sulfobenzoyl side chains for use as proton-exchange membranes.
2010 Dec
Monoclinic CuO nanoflowers on resin support: recyclable catalyst to obtain perylene compound.
2010 Dec 14
2,7-Bis(prop-2-yn-1-yl-oxy)naphthalene.
2010 Jun 9
A new group of aromatic prenyltransferases in fungi, catalyzing a 2,7-dihydroxynaphthalene 3-dimethylallyl-transferase reaction.
2010 May 28
Photoinduced formation of shape-selective Pt nanoparticles.
2010 May 4
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 19:05:06 GMT 2023
Edited
by admin
on Fri Dec 15 19:05:06 GMT 2023
Record UNII
0TO8E448UD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
2,7-NAPHTHALENEDIOL
INCI  
INCI  
Official Name English
2,7-DIHYDROXYNAPHTHALENE
Systematic Name English
2,7-NAPHTHALENEDIOL [INCI]
Common Name English
NSC-407541
Code English
C.I. 76645
Code English
C.I.-76645
Code English
CI-76645
Code English
CI 76645
Code English
Code System Code Type Description
ECHA (EC/EINECS)
209-478-7
Created by admin on Fri Dec 15 19:05:06 GMT 2023 , Edited by admin on Fri Dec 15 19:05:06 GMT 2023
PRIMARY
EPA CompTox
DTXSID2060387
Created by admin on Fri Dec 15 19:05:06 GMT 2023 , Edited by admin on Fri Dec 15 19:05:06 GMT 2023
PRIMARY
NSC
407541
Created by admin on Fri Dec 15 19:05:06 GMT 2023 , Edited by admin on Fri Dec 15 19:05:06 GMT 2023
PRIMARY
PUBCHEM
11397
Created by admin on Fri Dec 15 19:05:06 GMT 2023 , Edited by admin on Fri Dec 15 19:05:06 GMT 2023
PRIMARY
CAS
582-17-2
Created by admin on Fri Dec 15 19:05:06 GMT 2023 , Edited by admin on Fri Dec 15 19:05:06 GMT 2023
PRIMARY
FDA UNII
0TO8E448UD
Created by admin on Fri Dec 15 19:05:06 GMT 2023 , Edited by admin on Fri Dec 15 19:05:06 GMT 2023
PRIMARY
MESH
C107946
Created by admin on Fri Dec 15 19:05:06 GMT 2023 , Edited by admin on Fri Dec 15 19:05:06 GMT 2023
PRIMARY