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-HXUWFJFHSA-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-/m1/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 16:47:27 GMT 2023
by
admin
on
Fri Dec 15 16:47:27 GMT 2023
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Record UNII |
Z61JQF40LJ
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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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RACEMATE -> ENANTIOMER |