200,000+ products from a single source!
sales@angenechem.com
Home > Other Building Blocks > 235-08-5
235-08-5 | [1,2,4]Triazolo[4,3-a]quinoxaline
CAS No: 235-08-5 Catalog No: AG002NF0 MDL No:
Product Description
Catalog Number:
AG002NF0
Chemical Name:
[1,2,4]Triazolo[4,3-a]quinoxaline
CAS Number:
235-08-5
Molecular Formula:
C9H6N4
Molecular Weight:
170.1707
IUPAC Name:
[1,2,4]triazolo[4,3-a]quinoxaline
InChI:
InChI=1S/C9H6N4/c1-2-4-8-7(3-1)10-5-9-12-11-6-13(8)9/h1-6H
InChI Key:
QNSRYVDGWDXBHV-UHFFFAOYSA-N
SMILES:
c1ccc2c(c1)n1cnnc1cn2
Properties
Complexity:
196
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
170.059g/mol
Formal Charge:
0
Heavy Atom Count:
13
Hydrogen Bond Acceptor Count:
3
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
170.175g/mol
Monoisotopic Mass:
170.059g/mol
Rotatable Bond Count:
0
Topological Polar Surface Area:
43.1A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
1.5
Literature
| Title | Journal |
|---|---|
| Synthesis, ligand-receptor modeling studies and pharmacological evaluation of novel 4-modified-2-aryl-1,2,4-triazolo[4,3-a]quinoxalin-1-one derivatives as potent and selective human A3 adenosine receptor antagonists. | Bioorganic & medicinal chemistry 20080601 |
| Synthesis of some new quinoxalines and 1,2,4-triazolo[4,3-a]-quinoxalines for evaluation of in vitro antitumor and antimicrobial activities. | Archiv der Pharmazie 20061001 |
| Synthesis and antibacterial activity of fused 1, 2, 4-triazolo[4, 3-a]quinoxaline and oxopyrimido[2', 1':5, 1]-1, 2, 4-triazolo[4, 3-a]quinoxaline derivatives. | Archiv der Pharmazie 20020801 |
Related Products
Featured Products
© 2019 Angene International Limited. All rights Reserved.