Details
Stereochemistry | ACHIRAL |
Molecular Formula | C13H12O2 |
Molecular Weight | 200.2332 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=CC2=CC=C(C=C2C=C1)C(C)=O
InChI
InChIKey=GGWCZBGAIGGTDA-UHFFFAOYSA-N
InChI=1S/C13H12O2/c1-9(14)10-3-4-12-8-13(15-2)6-5-11(12)7-10/h3-8H,1-2H3
Molecular Formula | C13H12O2 |
Molecular Weight | 200.2332 |
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 |
---|---|---|
High-performance liquid chromatographic method development and validation for the simultaneous quantitation of naproxen sodium and pseudoephedrine hydrochloride impurities. | 2001 Mar |
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Enantioselective hydrolysis of naproxen ethyl ester catalyzed by monoclonal antibodies. | 2002 Jul |
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Simultaneous determination of naproxen and related compounds by HPLC using porous graphitic carbon column. | 2003 Aug 8 |
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Biodegradation of the analgesic naproxen by Trametes versicolor and identification of intermediates using HPLC-DAD-MS and NMR. | 2010 Apr |
Patents
Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 08:35:26 GMT 2023
by
admin
on
Sat Dec 16 08:35:26 GMT 2023
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Record UNII |
61VBH3537C
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Record Status |
Validated (UNII)
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Record Version |
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Related Record | Type | Details | ||
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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