3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide
- Molecular formula
- C6H8ClN7O
- CAS Number
- 82625-39-0
- IUPAC Name
- 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide
- Molecular Weight
- 231.59g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 2.1000g/cm3
- Synonyms
- 3-Amino-6-chloropyrazinamidoguanidine
Identification
Interesting Facts about 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide
3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide is a fascinating compound that attracts attention due to its unique structural features and potential applications. Here are some intriguing aspects:
- Bioactivity: This compound belongs to a class of molecules that exhibit significant biological activity, making them of interest in medicinal chemistry. Its structure suggests potential use as a pharmacological agent in various therapeutic areas.
- Structural Insights: The presence of both amino and guanidino functional groups gives this compound unique reactivity and interaction capabilities that can be crucial in designing new drugs or agrochemicals.
- Research Potential: The compound serves as a lead structure for synthesis and modification, opening the door for researchers to explore derivatives that may enhance efficacy or reduce toxicity.
- Chlorine Atom: The incorporation of a chlorine atom can alter the lipophilicity and metabolic stability of the molecule, factors that are critical in the optimization process of drug development.
As scientists, the exploration of compounds like 3-amino-6-chloro-N-guanidino-pyrazine-2-carboxamide not only broadens our understanding of chemical interactions but also contributes to advancements in therapeutic methodologies. Exploring its interplay within various biological systems continues to inspire ongoing research in the field.
Overall, the journey into the world of this compound exemplifies the intersection of chemistry, biology, and pharmacology, showcasing how fundamental research can lead to groundbreaking discoveries.