Ethyl 2-ethoxyquinoline-1-carboxylate
- Molecular formula
- C14H15NO3
- CAS Number
- 622-96-8
- IUPAC Name
- ethyl 2-ethoxy-2H-quinoline-1-carboxylate
- Molecular Weight
- 247.28g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.1120g/cm3
- Synonyms
- 16357-59-8
Identification
Interesting Facts about Ethyl 2-Ethoxy-2H-Quinoline-1-Carboxylate
Ethyl 2-ethoxy-2H-quinoline-1-carboxylate is an intriguing compound that belongs to the class of quinolines, known for their diverse biological activities and applications in medicinal chemistry. This compound is notable for its unique chemical structure and properties, making it a subject of interest across various fields of research. Here are some fascinating insights:
- Structural Versatility: The presence of the ethoxy group and the carboxylate functionality in its structure allows for various chemical modifications, enabling scientists to explore a range of derivatives with potentially enhanced activities.
- Biological Activity: Compounds featuring quinoline moieties, such as ethyl 2-ethoxy-2H-quinoline-1-carboxylate, have been studied for various pharmacological activities, including antimalarial, antimicrobial, and anticancer properties.
- Synthesis Techniques: The synthesis of this compound often involves innovative methods, including multicomponent reactions that showcase the versatility of organic chemistry in creating complex molecules from simpler starting materials.
- Research Applications: Due to its quinoline backbone, this compound holds promising implications in drug discovery and development, particularly in the search for new therapies against resistant microbial strains.
As researchers continue to unravel the potential of ethyl 2-ethoxy-2H-quinoline-1-carboxylate, its role could expand within the realms of medicinal chemistry and materials science, affirming the significance of exploring quinoline derivatives and their impact on modern scientific advancements.