U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS
This repository is under review for potential modification in compliance with Administration directives.

Details

Stereochemistry ABSOLUTE
Molecular Formula C16H17F3N2O5
Molecular Weight 374.3118
Optical Activity UNSPECIFIED
Defined Stereocenters 1 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SL-251188

SMILES

COC[C@@H]1CN(C(=O)O1)C2=NOC3=C2C=CC(OCCCC(F)(F)F)=C3

InChI

InChIKey=SQMNCLANJWZZOG-NSHDSACASA-N
InChI=1S/C16H17F3N2O5/c1-23-9-11-8-21(15(22)25-11)14-12-4-3-10(7-13(12)26-20-14)24-6-2-5-16(17,18)19/h3-4,7,11H,2,5-6,8-9H2,1H3/t11-/m0/s1

HIDE SMILES / InChI

Molecular Formula C16H17F3N2O5
Molecular Weight 374.3118
Charge 0
Count
Stereochemistry ABSOLUTE
Additional Stereochemistry No
Defined Stereocenters 1 / 1
E/Z Centers 0
Optical Activity UNSPECIFIED

Approval Year

Substance Class Chemical
Created
by admin
on Tue Apr 01 16:41:14 GMT 2025
Edited
by admin
on Tue Apr 01 16:41:14 GMT 2025
Record UNII
A8C48J5JCP
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SL-25.1188
Preferred Name English
SL-251188
Code English
SL251188
Code English
2-OXAZOLIDINONE, 5-(METHOXYMETHYL)-3-(6-(4,4,4-TRIFLUOROBUTOXY)-1,2-BENZISOXAZOL-3-YL)-, (5S)-
Systematic Name English
(5S)-5-(METHOXYMETHYL)-3-(6-(4,4,4-TRIFLUOROBUTOXY)-1,2-BENZISOXAZOL-3-YL)-2-OXAZOLIDINONE
Systematic Name English
2-OXAZOLIDINONE, 5-(METHOXYMETHYL)-3-(6-(4,4,4-TRIFLUOROBUTOXY)-1,2-BENZISOXAZOL-3-YL)-, (S)-
Systematic Name English
Code System Code Type Description
MANUFACTURER PRODUCT INFORMATION
SL-251188
Created by admin on Tue Apr 01 16:41:14 GMT 2025 , Edited by admin on Tue Apr 01 16:41:14 GMT 2025
PRIMARY 26 Aug 2004 Aventis has merged with Sanofi-Synthelabo to form Sanofi-Aventis 25 Sep 2002 Discontinued - Phase-I for Alzheimer's disease in Europe (unspecified route) 06 Dec 1999 New profile
EPA CompTox
DTXSID00430924
Created by admin on Tue Apr 01 16:41:14 GMT 2025 , Edited by admin on Tue Apr 01 16:41:14 GMT 2025
PRIMARY
FDA UNII
A8C48J5JCP
Created by admin on Tue Apr 01 16:41:14 GMT 2025 , Edited by admin on Tue Apr 01 16:41:14 GMT 2025
PRIMARY
PUBCHEM
9799696
Created by admin on Tue Apr 01 16:41:14 GMT 2025 , Edited by admin on Tue Apr 01 16:41:14 GMT 2025
PRIMARY
CAS
185835-97-6
Created by admin on Tue Apr 01 16:41:14 GMT 2025 , Edited by admin on Tue Apr 01 16:41:14 GMT 2025
PRIMARY
Related Record Type Details
LABELED -> NON-LABELED
Related Record Type Details
ACTIVE MOIETY