Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate
- Molecular formula
- C14H12O5
- CAS Number
- 3333-23-7
- IUPAC Name
- ethyl 3-acetyl-2-oxo-chromene-6-carboxylate
- Molecular Weight
- 275.26g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.2970g/cm3
- Synonyms
- 6468-75-3
Identification
Interesting Facts About Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate
Ethyl 3-acetyl-2-oxo-chromene-6-carboxylate is a fascinating compound that showcases the intricate world of organic chemistry. This compound belongs to the chromene family, which are derivatives of chromen-4-one, a naturally occurring structure that plays significant roles in various biological processes.
Key Characteristics
- Biological Activity: Compounds like ethyl 3-acetyl-2-oxo-chromene-6-carboxylate often exhibit remarkable biological activities, including antioxidant, anti-inflammatory, and even anticancer properties, making them subjects of intense research.
- Synthetic Utility: This compound serves as a precursor in the synthesis of more complex organic molecules. Its versatile structure enables it to participate in multiple reactions, thus expanding its applicability in various fields.
- Research Interest: The study of chromenes is significant in medicinal chemistry, as scientists explore their potential in drug development due to their diverse pharmacological profiles.
Quote from Chemistry Insight
"Every compound tells a story—unfolding layers of reactivity, biological significance, and potential applications." This statement resonates profoundly within the context of ethyl 3-acetyl-2-oxo-chromene-6-carboxylate, inviting both scientists and students alike to delve deeper into its wonders.
In summary, ethyl 3-acetyl-2-oxo-chromene-6-carboxylate not only highlights the complexity of organic molecules but also paves the way for innovative research in chemistry and beyond. Its potential applications and biological significance are truly what make chemistry an exciting field to explore!