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Details

Stereochemistry ACHIRAL
Molecular Formula C17H13ClN4
Molecular Weight 308.765
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 7-CHLORO-1-METHYL-5-PHENYL(1,2,4)TRIAZOLO(4,3-A)QUINOLIN-4-AMINE

SMILES

CC1=NN=C2N1C3=C(C=C(Cl)C=C3)C(C4=CC=CC=C4)=C2N

InChI

InChIKey=UZCOFCPJYLEACT-UHFFFAOYSA-N
InChI=1S/C17H13ClN4/c1-10-20-21-17-16(19)15(11-5-3-2-4-6-11)13-9-12(18)7-8-14(13)22(10)17/h2-9H,19H2,1H3

HIDE SMILES / InChI

Molecular Formula C17H13ClN4
Molecular Weight 308.765
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
CE as orthogonal technique to HPLC for alprazolam degradation product identification.
2006 Jun
Isolation, identification and determination of the major degradation product in alprazolam tablets during their stability assay.
2007 Jun 28
Patents

Patents

Substance Class Chemical
Created
by admin
on Sat Dec 16 06:52:46 UTC 2023
Edited
by admin
on Sat Dec 16 06:52:46 UTC 2023
Record UNII
R6K8F234S5
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
7-CHLORO-1-METHYL-5-PHENYL(1,2,4)TRIAZOLO(4,3-A)QUINOLIN-4-AMINE
Systematic Name English
(1,2,4)TRIAZOLO(4,3-A)QUINOLIN-4-AMINE, 7-CHLORO-1-METHYL-5-PHENYL-
Systematic Name English
ALPRAZOLAM IMPURITY G [EP IMPURITY]
Common Name English
Code System Code Type Description
CAS
448950-89-8
Created by admin on Sat Dec 16 06:52:46 UTC 2023 , Edited by admin on Sat Dec 16 06:52:46 UTC 2023
PRIMARY
EPA CompTox
DTXSID00196331
Created by admin on Sat Dec 16 06:52:46 UTC 2023 , Edited by admin on Sat Dec 16 06:52:46 UTC 2023
PRIMARY
PUBCHEM
69567153
Created by admin on Sat Dec 16 06:52:46 UTC 2023 , Edited by admin on Sat Dec 16 06:52:46 UTC 2023
PRIMARY
FDA UNII
R6K8F234S5
Created by admin on Sat Dec 16 06:52:46 UTC 2023 , Edited by admin on Sat Dec 16 06:52:46 UTC 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
total: not more than the area of the principal peak in the chromatogram obtained with reference solution (b) (0.25 per cent)
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP