2-Iodo-3,5-dimethylpyrazine
Names and Identifiers of 2-Iodo-3,5-dimethylpyrazine
CAS Number |
99969-02-5 |
|---|---|
MDL Number |
MFCD25969842 |
IUPAC Name |
2-iodo-3,5-dimethylpyrazine |
InChI |
InChI=1S/C6H7IN2/c1-4-3-8-6(7)5(2)9-4/h3H,1-2H3 |
InChIKey |
QROPUYBEEZUNIK-UHFFFAOYSA-N |
Canonical SMILES |
CC1=CN=C(C(=N1)C)I |
UNSPSC Code |
12352100 |
Physical and chemical properties of 2-Iodo-3,5-dimethylpyrazine
H Bond Acceptors |
2 |
|---|---|
H Bond Donors |
0 |
LogP |
0.762173403333333 |
Molecular Formula |
C6H7IN2 |
Molecular Weight |
234.04 |
Safety Information of 2-Iodo-3,5-dimethylpyrazine
Applications of 2-Iodo-3,5-dimethylpyrazine
2-Iodo-3,5-dimethylpyrazine has potential applications in several areas:
- Pharmaceuticals: Its unique structure may allow it to serve as a lead compound in drug discovery efforts targeting specific diseases.
- Agrochemicals: The compound could be explored for use in developing new pesticides or herbicides due to its biological activity.
- Flavoring Agents: Similar pyrazines are often utilized in food chemistry for their distinctive aromas, suggesting potential applications in flavoring.
Interaction Studies of 2-Iodo-3,5-dimethylpyrazine
Interaction studies involving 2-iodo-3,5-dimethylpyrazine focus on its reactivity with biological macromolecules such as proteins and nucleic acids. Preliminary research indicates that halogenated pyrazines may enhance binding affinity to certain targets compared to their non-halogenated analogs. Further studies are required to fully elucidate these interactions and their implications for drug design.
Biological Activity of 2-Iodo-3,5-dimethylpyrazine
Research indicates that compounds similar to 2-iodo-3,5-dimethylpyrazine may exhibit various biological activities. For instance, pyrazines are known to possess antimicrobial properties and may act as inhibitors of certain enzymes. Additionally, some studies suggest that halogenated pyrazines can display enhanced biological activity due to their ability to interact with biological targets more effectively than their non-halogenated counterparts.
Physical sample testing spectrum (NMR) of 2-Iodo-3,5-dimethylpyrazine
