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

Details

Stereochemistry RACEMIC
Molecular Formula C17H12Cl2N2O3
Molecular Weight 363.195
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Lorazepam acetate

SMILES

CC(=O)OC1N=C(C2=CC=CC=C2Cl)C3=CC(Cl)=CC=C3NC1=O

InChI

InChIKey=CYDZMDOLVUBPNL-UHFFFAOYSA-N
InChI=1S/C17H12Cl2N2O3/c1-9(22)24-17-16(23)20-14-7-6-10(18)8-12(14)15(21-17)11-4-2-3-5-13(11)19/h2-8,17H,1H3,(H,20,23)

HIDE SMILES / InChI

Molecular Formula C17H12Cl2N2O3
Molecular Weight 363.195
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Approval Year

PubMed

PubMed

TitleDatePubMed
Stereoselective kinetics of warfarin binding to human serum albumin: effect of an allosteric interaction.
2002-05-15
Recurrent complex partial status epilepticus associated with tiagabine rechallenge.
2002-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:07:26 GMT 2025
Edited
by admin
on Mon Mar 31 18:07:26 GMT 2025
Record UNII
Y4HA6DWZ18
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
Lorazepam acetate
Common Name English
LORAZEPAM RELATED COMPOUND A
USP   USP-RS  
Preferred Name English
2H-1,4-BENZODIAZEPIN-2-ONE, 3-(ACETYLOXY)-7-CHLORO-5-(2-CHLOROPHENYL)-1,3-DIHYDRO-
Systematic Name English
LORAZEPAM IMPURITY B [EP IMPURITY]
Common Name English
(3RS)-7-CHLORO-5-(2-CHLOROPHENYL)-2-OXO-2,3-DIHYDRO-1H-1,4-BENZODIAZEPIN-3-YL ACETATE
Systematic Name English
2H-1,4-BENZODIAZEPIN-2-ONE, 7-CHLORO-5-(O-CHLOROPHENYL)-1,3-DIHYDRO-3-HYDROXY-, ACETATE
Systematic Name English
RO-7-8407
Code English
LORAZEPAM RELATED COMPOUND A [USP-RS]
Common Name English
LORAZEPAM ACETATE, (±)-
Common Name English
LORAZEPAM RELATED COMPOUND A [USP IMPURITY]
Common Name English
Code System Code Type Description
PUBCHEM
17836
Created by admin on Mon Mar 31 18:07:26 GMT 2025 , Edited by admin on Mon Mar 31 18:07:26 GMT 2025
PRIMARY
MESH
C028245
Created by admin on Mon Mar 31 18:07:26 GMT 2025 , Edited by admin on Mon Mar 31 18:07:26 GMT 2025
PRIMARY
CAS
2848-96-6
Created by admin on Mon Mar 31 18:07:26 GMT 2025 , Edited by admin on Mon Mar 31 18:07:26 GMT 2025
PRIMARY
RS_ITEM_NUM
1370327
Created by admin on Mon Mar 31 18:07:26 GMT 2025 , Edited by admin on Mon Mar 31 18:07:26 GMT 2025
PRIMARY
ECHA (EC/EINECS)
220-653-7
Created by admin on Mon Mar 31 18:07:26 GMT 2025 , Edited by admin on Mon Mar 31 18:07:26 GMT 2025
PRIMARY
FDA UNII
Y4HA6DWZ18
Created by admin on Mon Mar 31 18:07:26 GMT 2025 , Edited by admin on Mon Mar 31 18:07:26 GMT 2025
PRIMARY
EPA CompTox
DTXSID00951169
Created by admin on Mon Mar 31 18:07:26 GMT 2025 , Edited by admin on Mon Mar 31 18:07:26 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> IMPURITY