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Details

Stereochemistry RACEMIC
Molecular Formula C18H15ClN2O3
Molecular Weight 342.776
Optical Activity ( + / - )
Defined Stereocenters 0 / 1
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of TEMAZEPAM ACETATE

SMILES

CN1C2=C(C=C(Cl)C=C2)C(=NC(OC(C)=O)C1=O)C3=CC=CC=C3

InChI

InChIKey=PTWWAHZQIATUFG-UHFFFAOYSA-N
InChI=1S/C18H15ClN2O3/c1-11(22)24-17-18(23)21(2)15-9-8-13(19)10-14(15)16(20-17)12-6-4-3-5-7-12/h3-10,17H,1-2H3

HIDE SMILES / InChI

Molecular Formula C18H15ClN2O3
Molecular Weight 342.776
Charge 0
Count
Stereochemistry RACEMIC
Additional Stereochemistry No
Defined Stereocenters 0 / 1
E/Z Centers 0
Optical Activity ( + / - )

Description

Information related to the biological or to the pharmacological activity of temazepam acetate is absent.

Approval Year

Conditions

Conditions

ConditionModalityTargetsHighest PhaseProduct

Sample Use Guides

In Vivo Use Guide
Unknown
Route of Administration: Unknown
In Vitro Use Guide
Unknown
Substance Class Chemical
Created
by admin
on Mon Mar 31 23:29:40 GMT 2025
Edited
by admin
on Mon Mar 31 23:29:40 GMT 2025
Record UNII
9F3H3E4BIM
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
TEMAZEPAM ACETATE
Common Name English
3-ACETOXYDIAZEPAM
Preferred Name English
2H-1,4-BENZODIAZEPIN-2-ONE, 3-(ACETYLOXY)-7-CHLORO-1,3-DIHYDRO-1-METHYL-5-PHENYL
Systematic Name English
TEMAZEPAM ACETATE, (RS)-
Common Name English
(3RS)-7-CHLORO-1-METHYL-2-OXO-5-PHENYL-2,3-DIHYDRO-1H-1,4-BENZODIAZEPIN-3-YL ACETATE
Systematic Name English
TEMAZEPAM IMPURITY C [EP IMPURITY]
Common Name English
TEMAZEPAM IMPURITY, O-ACETYL TEMAZEPAM- [USP IMPURITY]
Common Name English
Code System Code Type Description
PUBCHEM
86793
Created by admin on Mon Mar 31 23:29:40 GMT 2025 , Edited by admin on Mon Mar 31 23:29:40 GMT 2025
PRIMARY
EPA CompTox
DTXSID00940311
Created by admin on Mon Mar 31 23:29:40 GMT 2025 , Edited by admin on Mon Mar 31 23:29:40 GMT 2025
PRIMARY
ECHA (EC/EINECS)
242-597-2
Created by admin on Mon Mar 31 23:29:40 GMT 2025 , Edited by admin on Mon Mar 31 23:29:40 GMT 2025
PRIMARY
DRUG BANK
DB14671
Created by admin on Mon Mar 31 23:29:40 GMT 2025 , Edited by admin on Mon Mar 31 23:29:40 GMT 2025
PRIMARY
CAS
18818-64-9
Created by admin on Mon Mar 31 23:29:40 GMT 2025 , Edited by admin on Mon Mar 31 23:29:40 GMT 2025
PRIMARY
FDA UNII
9F3H3E4BIM
Created by admin on Mon Mar 31 23:29:40 GMT 2025 , Edited by admin on Mon Mar 31 23:29:40 GMT 2025
PRIMARY
Related Record Type Details
ENANTIOMER -> RACEMATE
ENANTIOMER -> RACEMATE
Related Record Type Details
PARENT -> IMPURITY