sales@angenesci.com
Login | Register
logo
Structures Search
Home Other Building Blocks Quinoxaline, 2,3-diphenyl-

Quinoxaline, 2,3-diphenyl-

CAS No.:
1684-14-6
Catalog Number:
AG001Y1N
Molecular Formula:
C20H14N2
Molecular Weight:
282.3386
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
98%
1 week
United States
$59
- +
25g
1 week
United States
$228
- +
Product Description
Catalog Number:
AG001Y1N
Chemical Name:
Quinoxaline, 2,3-diphenyl-
CAS Number:
1684-14-6
Molecular Formula:
C20H14N2
Molecular Weight:
282.3386
MDL Number:
MFCD00014659
IUPAC Name:
2,3-diphenylquinoxaline
InChI:
InChI=1S/C20H14N2/c1-3-9-15(10-4-1)19-20(16-11-5-2-6-12-16)22-18-14-8-7-13-17(18)21-19/h1-14H
InChI Key:
RSNQVABHABAKEZ-UHFFFAOYSA-N
SMILES:
c1ccc(cc1)c1nc2ccccc2nc1c1ccccc1
EC Number:
216-865-4
NSC Number:
15232
Properties
Complexity:
310  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
282.116g/mol
Formal Charge:
0
Heavy Atom Count:
22  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
282.346g/mol
Monoisotopic Mass:
282.116g/mol
Rotatable Bond Count:
2  
Topological Polar Surface Area:
25.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
4.5  
Literature
Title Journal
2,3-Diphenyl-quinoxalin-1-ium chloride. Acta crystallographica. Section E, Structure reports online 20100701
Synthesis and photophysical studies of iridium complexes of new 2,3-diphenylquinoxaline derivatives for organic light-emitting diodes. Journal of nanoscience and nanotechnology 20091201
DNA oxidative cleavage induced by the novel peptide derivatives of 3-(quinoxalin-6-yl)alanine in combination with Cu(II) or Fe(II) ions. Bioinorganic chemistry and applications 20090101
Expression of the prohelicity of bis-cyclomanganated 2,3-diphenylquinoxaline through reactions with diaryldiazomethanes. Chemical communications (Cambridge, England) 20020321
Properties