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Details

Stereochemistry ACHIRAL
Molecular Formula C12H6O3
Molecular Weight 198.1742
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NAPHTHALIC ANHYDRIDE

SMILES

O=C1OC(=O)C2=CC=CC3=C2C1=CC=C3

InChI

InChIKey=GRSMWKLPSNHDHA-UHFFFAOYSA-N
InChI=1S/C12H6O3/c13-11-8-5-1-3-7-4-2-6-9(10(7)8)12(14)15-11/h1-6H

HIDE SMILES / InChI

Molecular Formula C12H6O3
Molecular Weight 198.1742
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Evaluation of naphthal-NU, a 2-chloroethylnitrosourea derivative of naphthalimide, as a mixed-function anticancer agent.
2002 Mar
Inosine protects against the development of diabetes in multiple-low-dose streptozotocin and nonobese diabetic mouse models of type 1 diabetes.
2003 Mar-Apr
Line shapes and satellites in high-resolution x-ray photoelectron spectra of large pi-conjugated organic molecules.
2004 Nov 22
A comparison of fine structures in high-resolution x-ray-absorption spectra of various condensed organic molecules.
2005 Jul 22
Cloning, functional expression, and characterization of CYP709C1, the first sub-terminal hydroxylase of long chain fatty acid in plants. Induction by chemicals and methyl jasmonate.
2005 Oct 28
Use of fourier transform infrared spectroscopy to follow the heterocumulene aided thermal dehydration of phthalic and naphthalic acids.
2006 Dec
Prevention of cadmium induced lipid peroxidation, depletion of some antioxidative enzymes and glutathione by a series of novel organoselenocyanates.
2006 Nov
Transformation of PAHs during ethanol-Fenton treatment of an aged gasworks' soil.
2006 Nov
6-Oxobenz[de]isoquinolino[2,1-a]benzimidazolium chloride monohydrate.
2007 Dec 6
Synthesis of new amonafide analogues via coupling reaction and their cytotoxic evaluation and DNA-binding studies.
2009 Jan 15
Gas phase and bulk ultraviolet photoemission spectroscopy of 3,4,9,10-perylene-tetracarboxylic dianhydride, 1,4,5,8-naphthalene-tetracarboxylic dianhydride, and 1,8-naphthalene-dicarboxylic anhydride.
2009 Jul 21
cyclo-Tetra-kis(μ-naphthalene-1,8-dicarboxyl-ato)tetra-kis-[diaqua-(2,2'-bipyridine)-manganese(II)] tetra-hydrate.
2010 Nov 30
Patents
Substance Class Chemical
Created
by admin
on Sat Dec 16 02:15:46 GMT 2023
Edited
by admin
on Sat Dec 16 02:15:46 GMT 2023
Record UNII
32RS852X55
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NAPHTHALIC ANHYDRIDE
Systematic Name English
NSC-5747
Code English
Code System Code Type Description
CAS
81-84-5
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
PRIMARY
ALANWOOD
naphthalic anhydride
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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MESH
C012514
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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EPA CompTox
DTXSID4026505
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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FDA UNII
32RS852X55
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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WIKIPEDIA
1,8-Naphthalic anhydride
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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PUBCHEM
6693
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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ECHA (EC/EINECS)
201-380-2
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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HSDB
7371
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
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NSC
5747
Created by admin on Sat Dec 16 02:15:46 GMT 2023 , Edited by admin on Sat Dec 16 02:15:46 GMT 2023
PRIMARY