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Details

Stereochemistry RACEMIC
Molecular Formula C15H11ClN2O2
Molecular Weight 286.713
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-DEHYDROXY-3-OXO-4,5-DIHYDRO OXAZEPAM

SMILES

ClC1=CC=C2NC(=O)C(=O)NC(C3=CC=CC=C3)C2=C1

InChI

InChIKey=ZPRNOXLABKLWNP-UHFFFAOYSA-N
InChI=1S/C15H11ClN2O2/c16-10-6-7-12-11(8-10)13(9-4-2-1-3-5-9)18-15(20)14(19)17-12/h1-8,13H,(H,17,19)(H,18,20)

HIDE SMILES / InChI

Molecular Formula C15H11ClN2O2
Molecular Weight 286.713
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

Substance Class Chemical
Created
by admin
on Sat Dec 16 10:03:25 GMT 2023
Edited
by admin
on Sat Dec 16 10:03:25 GMT 2023
Record UNII
G2X40KX8CK
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-DEHYDROXY-3-OXO-4,5-DIHYDRO OXAZEPAM
Common Name English
OXAZEPAM RELATED COMPOUND A [USP-RS]
Common Name English
OXAZEPAM RELATED COMPOUND A
USP   USP-RS  
Common Name English
1H-1,4-BENZODIAZEPINE-2,3-DIONE, 7-CHLORO-4,5-DIHYDRO-5-PHENYL-
Systematic Name English
OXAZEPAM RELATED COMPOUND A [USP IMPURITY]
Common Name English
(5RS)-7-CHLORO-5-PHENYL-4,5-DIHYDRO-1H-1,4-BENZODIAZEPINE-2,3-DIONE
Systematic Name English
(±)-3-DEHYDROXY-3-OXO-4,5-DIHYDRO OXAZEPAM
Common Name English
OXAZEPAM IMPURITY A [EP IMPURITY]
Common Name English
Code System Code Type Description
FDA UNII
G2X40KX8CK
Created by admin on Sat Dec 16 10:03:25 GMT 2023 , Edited by admin on Sat Dec 16 10:03:25 GMT 2023
PRIMARY
RS_ITEM_NUM
1483017
Created by admin on Sat Dec 16 10:03:25 GMT 2023 , Edited by admin on Sat Dec 16 10:03:25 GMT 2023
PRIMARY
CAS
19554-95-1
Created by admin on Sat Dec 16 10:03:25 GMT 2023 , Edited by admin on Sat Dec 16 10:03:25 GMT 2023
PRIMARY
PUBCHEM
4196951
Created by admin on Sat Dec 16 10:03:25 GMT 2023 , Edited by admin on Sat Dec 16 10:03:25 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
For the calculation of contents, multiply the peak areas by 4.0
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP