(7-nitro-8-quinolyl) 3,4-dichlorobenzoate

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Identification

Molecular formula
C16H8Cl2N2O4
CAS Number
216343-63-6
IUPAC Name
(7-nitro-8-quinolyl) 3,4-dichlorobenzoate
Molecular Weight
396.15g/mol
Melting Point
(Celsius)
Boiling Point
(Celsius)
Density
1.6200g/cm3
Synonyms
BRN 1550763
Interesting facts

Exploring (7-nitro-8-quinolyl) 3,4-dichlorobenzoate

(7-nitro-8-quinolyl) 3,4-dichlorobenzoate is a fascinating compound that attracts attention in various fields of research, particularly in medicinal chemistry and materials science. Here are some key facts that amplify its significance:

  • Aromatic Amine Connections: This compound contains a quinoline structure, characterized by a fused ring system that contributes to its unique chemical properties.
  • Bioactivity: Compounds related to quinolines have been extensively studied for their potential biological activities, including antibacterial, antifungal, and antimalarial properties. This makes (7-nitro-8-quinolyl) 3,4-dichlorobenzoate an exciting candidate for further investigation in drug development.
  • Functional Group Diversity: As a derivative of benzoate, this compound showcases the versatility of functional groups, allowing for a variety of chemical reactions and transformations.
  • Fluorescent Properties: Many quinoline derivatives exhibit fluorescent properties, which could be leveraged in applications like organic light-emitting diodes (OLEDs) and fluorescent probes in biological imaging.

As noted by researchers, “The structural diversity presented by modifications on quinolines leads to a vast array of potential applications, from pharmaceuticals to optoelectronic materials.” This highlights the compound's potential impact across multiple scientific disciplines.

In summary, (7-nitro-8-quinolyl) 3,4-dichlorobenzoate is not just a chemical entity; it embodies a wealth of possibilities for innovation and discovery in the realms of chemistry and beyond.

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