Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H8N2 |
| Molecular Weight | 108.1411 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CCC1=NC=CN=C1
InChI
InChIKey=KVFIJIWMDBAGDP-UHFFFAOYSA-N
InChI=1S/C6H8N2/c1-2-6-5-7-3-4-8-6/h3-5H,2H2,1H3
| Molecular Formula | C6H8N2 |
| Molecular Weight | 108.1411 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Degradation of 2,5-dimethylpyrazine by Rhodococcus erythropolis strain DP-45 isolated from a waste gas treatment plant of a fishmeal processing company. | 2007-10 |
|
| Pyrazine derivatives in cigarette smoke inhibit hamster oviductal functioning. | 2004-05-12 |
|
| Thermochemical study of the ethylpyridine and ethylpyrazine isomers. | 2003-12-07 |
|
| Growth and angiogenesis are inhibited in vivo in developing tissues by pyrazine and its derivatives. | 2003-10 |
|
| Mechanisms responsible for the in vitro relaxation of ligustrazine on porcine left anterior descending coronary artery. | 2003-05-16 |
|
| Structure-activity relationship of ligands of uracil phosphoribosyltransferase from Toxoplasma gondii. | 1994-08-17 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 19:14:55 GMT 2025
by
admin
on
Mon Mar 31 19:14:55 GMT 2025
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| Record UNII |
0QO4LUV16Z
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| Record Status |
Validated (UNII)
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| Record Version |
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| Classification Tree | Code System | Code | ||
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JECFA EVALUATION |
2-ETHYLPYRAZINE
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