DEET
- Molecular formula
- C12H17NO2
- CAS Number
- 134-62-3
- IUPAC Name
- ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate
- Molecular Weight
- 271.35g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3290g/cm3
- Synonyms
- DECOQUINATE
Identification
Interesting Facts about Ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate
Ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate is a fascinating compound that falls within the realm of quinoline derivatives, renowned for their diverse range of biological activities. Quinoline compounds, in general, have intrigued scientists due to their role in medicinal chemistry and organic synthesis.
Key Highlights:
- Biological Activity: Quinoline derivatives, including this compound, are often explored for their potential antimicrobial, antimalarial, and anticancer activities, making them important in the field of drug discovery.
- Synthetic Versatility: The unique structure of quinolines allows for various chemical modifications, which can unleash different therapeutic properties and broaden their application spectra.
- Research Applications: Compounds like ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate are valuable in studies related to enzyme inhibition and receptor interaction, giving insights into complex biological processes.
- Quinoline Core: The quinoline skeleton itself is noteworthy since it can facilitate the formation of various heterocycles that are foundational to many natural products and pharmaceuticals.
As we delve deeper into the properties and functionalities of ethyl 6-decoxy-7-ethoxy-4-oxo-1H-quinoline-3-carboxylate, one can't help but appreciate the intricate balance between structure and activity that defines this compound and its potential applications in the realm of chemistry and medicine. The journey towards understanding such compounds not only enhances our chemical knowledge but also serves as a stepping stone towards innovative therapeutic modalities.