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
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
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
Title | Date | PubMed |
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Line shapes and satellites in high-resolution x-ray photoelectron spectra of large pi-conjugated organic molecules. | 2004 Nov 22 |
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Synthesis and evaluation of antioxidative properties of a series of organoselenium compounds. | 2005 Oct 15 |
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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 |
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Prevention of cadmium induced lipid peroxidation, depletion of some antioxidative enzymes and glutathione by a series of novel organoselenocyanates. | 2006 Nov |
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N-(4-Amino-phen-yl)-1,8-naphthalimide hemihydrate. | 2007 Dec 12 |
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6-Oxobenz[de]isoquinolino[2,1-a]benzimidazolium chloride monohydrate. | 2007 Dec 6 |
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N-(2-Hydroxy-ethyl)-1,8-naphthalimide. | 2009 May 7 |
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6-Nitro-2-(3-hydroxypropyl)-1H-benz[de]isoquinoline-1,3-dione, a potent antitumor agent, induces cell cycle arrest and apoptosis. | 2010 Dec 31 |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 02:15:46 GMT 2023
by
admin
on
Sat Dec 16 02:15:46 GMT 2023
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Record UNII |
32RS852X55
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Record Status |
Validated (UNII)
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Record Version |
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Code | English |
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81-84-5
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naphthalic anhydride
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C012514
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DTXSID4026505
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32RS852X55
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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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6693
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201-380-2
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7371
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5747
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