[3-(acetoxymethyl)quinoxalin-2-yl]methyl acetate
- Molecular formula
- C15H16N2O4
- CAS Number
- 161798-01-2
- IUPAC Name
- [3-(acetoxymethyl)quinoxalin-2-yl]methyl acetate
- Molecular Weight
- 288.29g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2686g/cm3
- Synonyms
- 2, 3-Bis(acetoxymethyl)quinoxaline
Identification
Interesting Facts about [3-(acetoxymethyl)quinoxalin-2-yl]methyl acetate
[3-(acetoxymethyl)quinoxalin-2-yl]methyl acetate is a fascinating compound that belongs to the quinoxaline family, which is known for its diverse range of biological activities. Here are some intriguing points about this compound:
- Biomedical Significance: Quinoxaline derivatives have been extensively studied for their potential therapeutic uses, including antibacterial, antifungal, and anticancer properties.
- Synthetic Versatility: The presence of the acetoxymethyl moiety enables the introduction of various functional groups, making it a valuable intermediate for synthetic chemistry.
- Unique Structure: The compound features a quinoxaline ring, which is a bicyclic structure known for its aromatic character. This framework contributes to the stability and reactivity of the compound in chemical reactions.
- Research Applications: Studies involving quinoxaline derivatives explore their role in pharmacology, material science, and organic synthesis, showcasing their wide applicability.
- Potential as a Molecular Probe: Due to its chemical structure, [3-(acetoxymethyl)quinoxalin-2-yl]methyl acetate may serve as a suitable candidate for molecular probes in biological studies, helping researchers understand complex biochemical pathways.
This compound's intriguing properties and structure not only make it essential for academic research but also spark curiosity in its potential applications within therapeutic disciplines. As researchers continue to unlock the secrets of quinoxaline derivatives, compounds like [3-(acetoxymethyl)quinoxalin-2-yl]methyl acetate will play a key role in advancing our understanding of chemical and biological interactions.