Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C16H18O3 |
| Molecular Weight | 258.3129 |
| Optical Activity | UNSPECIFIED |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCOC(=O)[C@@]([H])(C)c1ccc2cc(ccc2c1)OC
InChI
InChIKey=URNAYRDBUUZOIU-NSHDSACASA-N
InChI=1S/C16H18O3/c1-4-19-16(17)11(2)12-5-6-14-10-15(18-3)8-7-13(14)9-12/h5-11H,4H2,1-3H3/t11-/m0/s1
| Molecular Formula | C16H18O3 |
| Molecular Weight | 258.3129 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ABSOLUTE |
| Additional Stereochemistry | No |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Optical Activity | UNSPECIFIED |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Enantioselective hydrolysis of naproxen ethyl ester catalyzed by monoclonal antibodies. | 2002 Jul |
|
| Crystallization and preliminary X-ray diffraction studies of a fungal hydrolase from Ophiostoma novo-ulmi. | 2004 Oct |
|
| Spherezymes: a novel structured self-immobilisation enzyme technology. | 2008 Jan 31 |
|
| Lipase-catalyzed esterification of (S)-naproxen ethyl ester in supercritical carbon dioxide. | 2009 Dec |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Jun 26 02:12:56 UTC 2021
by
admin
on
Sat Jun 26 02:12:56 UTC 2021
|
| Record UNII |
978RJD689Y
|
| Record Status |
Validated (UNII)
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| Record Version |
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711615
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978RJD689Y
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31220-35-6
Created by
admin on Sat Jun 26 02:12:57 UTC 2021 , Edited by admin on Sat Jun 26 02:12:57 UTC 2021
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31220-35-6
Created by
admin on Sat Jun 26 02:12:57 UTC 2021 , Edited by admin on Sat Jun 26 02:12:57 UTC 2021
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UNSPECIFIED
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PARENT -> IMPURITY |
UNSPECIFIED
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