Home Other Building Blocks 2-Ethylpyrazine

2-Ethylpyrazine

CAS No.:
13925-00-3
Catalog Number:
AG003H6O
Molecular Formula:
C6H8N2
Molecular Weight:
108.1411
Pack Size
Purity
Availability
Location
Price(USD)
Quantity
  
1g
97%
In Stock USA
United States
$47
- +
5g
97%
In Stock USA
United States
$107
- +
Product Description
Catalog Number:
AG003H6O
Chemical Name:
2-Ethylpyrazine
CAS Number:
13925-00-3
Molecular Formula:
C6H8N2
Molecular Weight:
108.1411
MDL Number:
MFCD00006149
IUPAC Name:
2-ethylpyrazine
InChI:
InChI=1S/C6H8N2/c1-2-6-5-7-3-4-8-6/h3-5H,2H2,1H3
InChI Key:
KVFIJIWMDBAGDP-UHFFFAOYSA-N
SMILES:
CCc1cnccn1
EC Number:
237-691-5
UNII:
0QO4LUV16Z
FEMA Number:
3281
Properties
Complexity:
63.5  
Compound Is Canonicalized:
Yes
Covalently-Bonded Unit Count:
1  
Defined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Exact Mass:
108.069g/mol
Formal Charge:
0
Heavy Atom Count:
8  
Hydrogen Bond Acceptor Count:
2  
Hydrogen Bond Donor Count:
0
Isotope Atom Count:
0
Molecular Weight:
108.144g/mol
Monoisotopic Mass:
108.069g/mol
Rotatable Bond Count:
1  
Topological Polar Surface Area:
25.8A^2
Undefined Atom Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
XLogP3:
0.7  
Literature
Title Journal
Effect of sugars on liquid-vapour partition of volatile compounds in ready-to-drink coffee beverages. Journal of mass spectrometry : JMS 20120901
Similar odorants elicit different behavioral and physiological responses, some supersustained. The Journal of neuroscience : the official journal of the Society for Neuroscience 20110525
Degradation of 2,5-dimethylpyrazine by Rhodococcus erythropolis strain DP-45 isolated from a waste gas treatment plant of a fishmeal processing company. Biodegradation 20071001
Pyrazine derivatives in cigarette smoke inhibit hamster oviductal functioning. Reproductive biology and endocrinology : RB&E 20040101
Thermochemical study of the ethylpyridine and ethylpyrazine isomers. Organic & biomolecular chemistry 20031207
Growth and angiogenesis are inhibited in vivo in developing tissues by pyrazine and its derivatives. Toxicological sciences : an official journal of the Society of Toxicology 20031001
Mechanisms responsible for the in vitro relaxation of ligustrazine on porcine left anterior descending coronary artery. European journal of pharmacology 20030516
Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii. Biochemical pharmacology 19940817
Properties