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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=C3C(C=CC=C13)=CC=C2

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
6-Nitro-2-(3-hydroxypropyl)-1H-benz[de]isoquinoline-1,3-dione, a potent antitumor agent, induces cell cycle arrest and apoptosis.
2010-12-31
cyclo-Tetra-kis(μ-naphthalene-1,8-dicarboxyl-ato)tetra-kis-[diaqua-(2,2'-bipyridine)-manganese(II)] tetra-hydrate.
2010-11-30
Naphthalene-1,8-dicarb-oxy-lic anhydride: a monoclinic polymorph.
2010-09-25
Bis(μ-naphthalene-1,8-dicarboxyl-ato-κO:O)bis-[aqua-bis-(N,N'-dimethyl-formamide-κO)copper(II)].
2010-07-24
2-(tert-Butoxy-carbonyl-amino)-6-(1,3-dioxo-1H-2,3-dihydro-benzo[de]isoquinolin-2-yl)hexa-noic acid.
2010-04-28
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.
2009-07-21
N-(4-Chloro-phenyl)-1,8-naphthalimide.
2009-06-13
N-(2-Hydroxy-ethyl)-1,8-naphthalimide.
2009-05-07
Synthesis of new amonafide analogues via coupling reaction and their cytotoxic evaluation and DNA-binding studies.
2009-01-15
N-(4-Amino-phen-yl)-1,8-naphthalimide hemihydrate.
2007-12-12
6-Oxobenz[de]isoquinolino[2,1-a]benzimidazolium chloride monohydrate.
2007-12-06
Use of fourier transform infrared spectroscopy to follow the heterocumulene aided thermal dehydration of phthalic and naphthalic acids.
2006-12
Prevention of cadmium induced lipid peroxidation, depletion of some antioxidative enzymes and glutathione by a series of novel organoselenocyanates.
2006-11
Transformation of PAHs during ethanol-Fenton treatment of an aged gasworks' soil.
2006-11
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.
2005-10-28
Synthesis and evaluation of antioxidative properties of a series of organoselenium compounds.
2005-10-15
A comparison of fine structures in high-resolution x-ray-absorption spectra of various condensed organic molecules.
2005-07-22
Line shapes and satellites in high-resolution x-ray photoelectron spectra of large pi-conjugated organic molecules.
2004-11-22
Inosine protects against the development of diabetes in multiple-low-dose streptozotocin and nonobese diabetic mouse models of type 1 diabetes.
2003-07-17
Molecular complexes of antipsychotic pharmaceutical parent molecule phenothiazine and unsaturated acid anhydrides.
2003-05
Efficiency and cytotoxicity of resin-based desensitizing agents.
2002-10
Evaluation of naphthal-NU, a 2-chloroethylnitrosourea derivative of naphthalimide, as a mixed-function anticancer agent.
2002-03
Involvement of cytochrome P-450 enzyme activity in the selectivity and safening action of pyrazosulfuron-ethyl.
2001-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:11:32 GMT 2025
Edited
by admin
on Mon Mar 31 21:11:32 GMT 2025
Record UNII
32RS852X55
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NAPHTHALIC ANHYDRIDE
Systematic Name English
NSC-5747
Preferred Name English
Code System Code Type Description
CAS
81-84-5
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
PRIMARY
ALANWOOD
naphthalic anhydride
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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MESH
C012514
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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EPA CompTox
DTXSID4026505
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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FDA UNII
32RS852X55
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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WIKIPEDIA
1,8-Naphthalic anhydride
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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PUBCHEM
6693
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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ECHA (EC/EINECS)
201-380-2
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
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HSDB
7371
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
PRIMARY
NSC
5747
Created by admin on Mon Mar 31 21:11:32 GMT 2025 , Edited by admin on Mon Mar 31 21:11:32 GMT 2025
PRIMARY