Dinitroquinoxaline
ADVERTISEMENT
- Molecular formula
- C8H2N4O6
- CAS Number
- 2168-92-9
- IUPAC Name
- 6,7-dinitroquinoxaline-2,3-dione
- Molecular Weight
- 236.12g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.6500g/cm3
- Synonyms
- 6, 7-Dinitro-2, 3-quinoxalinedione
Identification
Interesting facts
Interesting Facts about 6,7-Dinitroquinoxaline-2,3-dione
6,7-Dinitroquinoxaline-2,3-dione is a fascinating compound extensively studied in the field of biochemistry and pharmacology. Here are some noteworthy points:
- Chemical Structure: This compound belongs to the quinoxaline family, characterized by a fused aromatic ring structure. The presence of electron-withdrawing nitro (-NO2) groups significantly impacts its chemical reactivity and biological activity.
- Biological Activity: It is known for its role as a potent inhibitor of certain enzymes and receptors. Research shows that derivatives of this compound exhibit neuroprotective effects and potential applications in treating neurological disorders.
- Research Applications: Scientists often utilize 6,7-dinitroquinoxaline-2,3-dione in neuropharmacological studies. For example, it acts as an antagonist for specific receptors, making it instrumental in dissecting neurotransmission pathways.
- Toxicology: Like many nitro compounds, it is vital to handle this chemical with care due to its potential toxic effects. Investigations into its safety profile reveal important considerations for laboratory practices.
- Historical Significance: The compound has contributed to various scientific advancements, particularly in understanding the mechanisms of synaptic transmission in the brain. Its study has uncovered important insights into how neurotransmitters affect cognitive functions.
Overall, 6,7-dinitroquinoxaline-2,3-dione exemplifies the intersection of chemistry and biology, highlighting the power of small molecules in influencing complex biological systems. As research continues, the potential for new therapeutic applications remains promising.