U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry RACEMIC
Molecular Formula C17H13ClN2O3
Molecular Weight 328.75
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of OXAZEPAM ACETATE

SMILES

CC(=O)OC1N=C(C2=CC=CC=C2)C3=C(NC1=O)C=CC(Cl)=C3

InChI

InChIKey=FYRWUTOZBRWYCS-UHFFFAOYSA-N
InChI=1S/C17H13ClN2O3/c1-10(21)23-17-16(22)19-14-8-7-12(18)9-13(14)15(20-17)11-5-3-2-4-6-11/h2-9,17H,1H3,(H,19,22)

HIDE SMILES / InChI

Molecular Formula C17H13ClN2O3
Molecular Weight 328.75
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Patents

Patents

Substance Class Chemical
Created
by admin
on Fri Dec 15 15:32:40 GMT 2023
Edited
by admin
on Fri Dec 15 15:32:40 GMT 2023
Record UNII
611V4315UA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
OXAZEPAM ACETATE
Common Name English
(±)-OXAZEPAM ACETATE
Common Name English
OXAZEPAM RELATED COMPOUND B
USP   USP-RS  
Common Name English
(3RS)-7-CHLORO-2-OXO-5-PHENYL-2,3-DIHYDRO-1H-1,4-BENZODIAZEPIN-3-YL ACETATE
Systematic Name English
OXAZEPAM IMPURITY B [EP IMPURITY]
Common Name English
OXAZEPAM RELATED COMPOUND B [USP IMPURITY]
Common Name English
3-ACETOXY-7-CHLORO-1,3-DIHYDRO-5-PHENYL-2H-1,4-BENZODIAZEPIN-2-ONE
Systematic Name English
(±)-OXAZEPAM 3-ACETATE
Common Name English
2H-1,4-BENZODIAZEPIN-2-ONE, 3-(ACETYLOXY)-7-CHLORO-1,3-DIHYDRO-5-PHENYL-
Systematic Name English
OXAZEPAM RELATED COMPOUND B [USP-RS]
Common Name English
Code System Code Type Description
ECHA (EC/EINECS)
217-359-6
Created by admin on Fri Dec 15 15:32:40 GMT 2023 , Edited by admin on Fri Dec 15 15:32:40 GMT 2023
PRIMARY
FDA UNII
611V4315UA
Created by admin on Fri Dec 15 15:32:40 GMT 2023 , Edited by admin on Fri Dec 15 15:32:40 GMT 2023
PRIMARY
PUBCHEM
102697
Created by admin on Fri Dec 15 15:32:40 GMT 2023 , Edited by admin on Fri Dec 15 15:32:40 GMT 2023
PRIMARY
CAS
1824-74-4
Created by admin on Fri Dec 15 15:32:40 GMT 2023 , Edited by admin on Fri Dec 15 15:32:40 GMT 2023
PRIMARY
DRUG BANK
DB14672
Created by admin on Fri Dec 15 15:32:40 GMT 2023 , Edited by admin on Fri Dec 15 15:32:40 GMT 2023
PRIMARY
RS_ITEM_NUM
1483028
Created by admin on Fri Dec 15 15:32:40 GMT 2023 , Edited by admin on Fri Dec 15 15:32:40 GMT 2023
PRIMARY
EPA CompTox
DTXSID40939582
Created by admin on Fri Dec 15 15:32:40 GMT 2023 , Edited by admin on Fri Dec 15 15:32:40 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
For the calculation of contents, multiply the peak areas by 1.1
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP