Coumarin 6

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Identification

Molecular formula
C14H10N2O2
CAS Number
38215-99-5
IUPAC Name
6-amino-3-(4-pyridyl)chromen-2-one
Molecular Weight
262.28g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.3540g/cm3
Synonyms
3390-71-4
Interesting facts

Interesting Facts about 6-amino-3-(4-pyridyl)chromen-2-one

6-amino-3-(4-pyridyl)chromen-2-one, often associated with pharmacological research, is an intriguing compound that showcases the fascinating intersection of chemistry and biology. Here are some compelling insights:

  • Versatile Structure: This compound features a chromenone backbone, which is known for its ability to participate in various chemical reactions. The presence of the amino and pyridine functional groups contributes to its rich chemical reactivity.
  • Pharmacological Potential: Research shows that derivatives of the chromenone framework have exhibited potential biological activities, including anti-inflammatory, antioxidant, and even anticancer properties. This positions 6-amino-3-(4-pyridyl)chromen-2-one as a candidate for further study in medicinal chemistry.
  • Receptor Interactions: Its structural features suggest potential interactions with various biological receptors, making it an interesting subject for drug design aimed at targeting specific pathways in diseases.
  • Synergistic Effects: The combination of the amino group and the pyridine ring can enhance the activity of this compound in biological systems, often resulting in synergistic effects that improve therapeutic outcomes.
  • Historical Context: Chromenones have been studied for decades, but the exploration of specific derivatives like 6-amino-3-(4-pyridyl)chromen-2-one is relatively new, indicating a growing interest in synthesizing and evaluating novel derivatives to expand their potential applications.

As research in this area continues to evolve, the implications of studying compounds like 6-amino-3-(4-pyridyl)chromen-2-one remain profound, influencing the development of new therapeutic agents and enhancing our understanding of bioactive molecules.

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