(7-nitro-8-quinolyl) naphthalene-2-carboxylate
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- Molecular formula
- C20H11N2O4
- CAS Number
- 99580-09-5
- IUPAC Name
- (7-nitro-8-quinolyl) naphthalene-2-carboxylate
- Molecular Weight
- 392.37g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.3823g/cm3
- Synonyms
- BRN 1550729
Identification
Interesting facts
Interesting Facts about (7-nitro-8-quinolyl) naphthalene-2-carboxylate
(7-nitro-8-quinolyl) naphthalene-2-carboxylate is a fascinating compound with numerous applications in the realm of chemistry and material science. Here are some intriguing aspects that showcase its unique properties:
- Fluorescent Properties: This compound exhibits strong fluorescence, making it a valuable indicator in various analytical methods. Its emission characteristics are often utilized in biological imaging and sensing applications.
- Intermolecular Interactions: The compound's molecular structure allows it to form extensive hydrogen bonding networks. This can enhance its stability and influence its solvation properties in different environments.
- Versatility in Synthesis: It can be synthesized through a series of reactions involving commercially available starting materials, allowing for flexibility in laboratory settings. This makes it a popular choice among researchers.
- Biological Relevance: Its derivatives have been studied for potential applications in pharmacology. The quinoline moiety is particularly noteworthy for its **bioactivity** against various pathogens.
- Innovative Applications: Beyond biological studies, it is also investigated for use in organic light-emitting diodes (OLEDs) and organic photovoltaic cells, contributing to advancements in sustainable energy technologies.
As noted by one researcher, "the unique arrangement of functional groups in this compound makes it a prime candidate for both theoretical research and practical applications." With ongoing studies, (7-nitro-8-quinolyl) naphthalene-2-carboxylate continues to inspire innovations across diverse scientific fields.