Details
| Stereochemistry | ABSOLUTE |
| Molecular Formula | C15H15NO3S |
| Molecular Weight | 289.35 |
| Optical Activity | ( - ) |
| Defined Stereocenters | 1 / 1 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
ONC(=O)C[S@+]([O-])C(C1=CC=CC=C1)C2=CC=CC=C2
InChI
InChIKey=CGNMLOKEMNBUAI-FQEVSTJZSA-N
InChI=1S/C15H15NO3S/c17-14(16-18)11-20(19)15(12-7-3-1-4-8-12)13-9-5-2-6-10-13/h1-10,15,18H,11H2,(H,16,17)/t20-/m0/s1
| Molecular Formula | C15H15NO3S |
| Molecular Weight | 289.35 |
| 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 |
|---|---|---|
| Enantioselective separation and determination of adrafinil and modafinil on Chiralcel OJ-H column in rat serum and urine using solid-phase extraction followed by HPLC. | 2009 Aug |
|
| Development of a validated LC method for enantiomeric separation and determination of adrafinil and its related substances on a Chiralcel OJ-H column connected to PDA and polarimetric detectors in series. | 2010 Nov |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 16:47:52 GMT 2023
by
admin
on
Fri Dec 15 16:47:52 GMT 2023
|
| Record UNII |
7J4NMN2710
|
| Record Status |
Validated (UNII)
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| Record Version |
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-
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DTXSID20654463
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7J4NMN2710
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827603-96-3
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admin on Fri Dec 15 16:47:52 GMT 2023 , Edited by admin on Fri Dec 15 16:47:52 GMT 2023
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| Related Record | Type | Details | ||
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RACEMATE -> ENANTIOMER |
