(7-nitro-8-quinolyl) naphthalene-2-carboxylate

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Identification

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
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.

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