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