Home Aldehydes Pyrazine-2-carbaldehyde

Pyrazine-2-carbaldehyde

CAS No.:
5780-66-5
Catalog Number:
AG0038MJ
Molecular Formula:
C5H4N2O
Molecular Weight:
108.0981
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
95%
In Stock USA
United States
$138
- +
5g
95%
In Stock USA
United States
$413
- +
10g
95%
In Stock USA
United States
$750
- +
25g
95%
In Stock USA
United States
$1500
- +
Product Description
Catalog Number:
AG0038MJ
Chemical Name:
Pyrazine-2-carbaldehyde
CAS Number:
5780-66-5
Molecular Formula:
C5H4N2O
Molecular Weight:
108.0981
MDL Number:
MFCD02179278
IUPAC Name:
pyrazine-2-carbaldehyde
InChI:
InChI=1S/C5H4N2O/c8-4-5-3-6-1-2-7-5/h1-4H
InChI Key:
DXBWJLDFSICTIH-UHFFFAOYSA-N
SMILES:
O=Cc1cnccn1
UNII:
EX42FX5JBS
Properties
Complexity:
84.5  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
108.032g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
3  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
108.1g/mol
Monoisotopic Mass:
108.032g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
42.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
-0.4  
Literature
Title Journal
Dichlorido[2-(3,5-dimethyl-1H-pyrazol-1-yl-κN(2))quinoline-κN]zinc. Acta crystallographica. Section E, Structure reports online 20120501
Discovery of a novel chemotype of potent human ENaC blockers using a bioisostere approach. Part 2: α-Branched quaternary amines. Bioorganic & medicinal chemistry letters 20120415
Discovery of a novel chemotype of potent human ENaC blockers using a bioisostere approach. Part 1: quaternary amines. Bioorganic & medicinal chemistry letters 20120115
Synthesis and characterization of organic impurities in bortezomib anhydride produced by a convergent technology. Scientia pharmaceutica 20120101
tert-Butyl 4-{[5-(4-chloro-phen-yl)-1-(4-fluoro-phen-yl)-1H-pyrazol-3-yl]carbon-yl}piperazine-1-carboxyl-ate. Acta crystallographica. Section E, Structure reports online 20101001
Characterization of a new series of non-covalent proteasome inhibitors with exquisite potency and selectivity for the 20S beta5-subunit. The Biochemical journal 20100915
Properties