(7-nitro-8-quinolyl) 4-chlorobenzoate
- Molecular formula
- C16H9ClNO4
- CAS Number
- 467458-09-7
- IUPAC Name
- (7-nitro-8-quinolyl) 4-chlorobenzoate
- Molecular Weight
- 314.70g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.4000g/cm3
- Appearance
- can vary depending on the form, such as crystalline or powder, and might exhibit a light color, often related to its aromatic structure combined with nitro groups.
- Synonyms
- BENZOIC ACID, p-CHLORO-, 7-NITRO-8-QUINOLYL ESTER
Identification
Interesting Facts about (7-nitro-8-quinolyl) 4-chlorobenzoate
(7-nitro-8-quinolyl) 4-chlorobenzoate is a fascinating compound that blends the properties of quinoline and benzoate derivatives. Its unique structure lends it specific characteristics and potential applications that intrigue chemists and researchers alike.
Key Features
- Bioactivity: This compound is often studied for its potential biological activities, including anti-bacterial and anti-fungal properties. Such activities are attributed to its ability to interact with various biological targets.
- Photophysical Properties: The compound exhibits interesting photophysical characteristics, making it useful in fields like fluorescent probes and sensors.
- Versatile Synthesis: The synthesis of (7-nitro-8-quinolyl) 4-chlorobenzoate can be achieved using various methods, highlighting its versatility in chemical synthesis.
Researchers have reported intriguing findings regarding its reactivity and utility. For instance, it has been noted that compounds containing the quinoline moiety can partake in *metal coordination* and *ligand exchange* processes, which can be of significant interest in coordination chemistry.
Applications
- Pharmaceutical Development: Its structure positions it as a candidate for drug development, particularly in the realm of anti-infective agents.
- Material Science: This compound's unique properties may also find applications in the development of advanced materials, such as organic light-emitting diodes (OLEDs).
In conclusion, the exploration of (7-nitro-8-quinolyl) 4-chlorobenzoate not only sheds light on its functional capabilities but also emphasizes the broader significance of quinoline derivatives in modern chemistry. This compound is a prime example of how specific chemical structures can lead to innovative applications and deepen our understanding of biological processes.