Kynurenic acid
- Molecular formula
- C10H7NO3
- CAS Number
- 492-27-3
- IUPAC Name
- 6-methyl-2-(3-pyridyl)quinoline-4-carboxylic acid
- Molecular Weight
- 189.17g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.5290g/cm3
- Appearance
- when powdered.
- Synonyms
- 5110-02-1
Identification
Interesting Facts about 6-methyl-2-(3-pyridyl)quinoline-4-carboxylic acid
6-methyl-2-(3-pyridyl)quinoline-4-carboxylic acid is a fascinating compound that belongs to the family of quinoline derivatives, which are known for their diverse biological activities. This compound has captured the attention of scientists due to its role in various fields, including pharmaceuticals and material science. Here are some interesting aspects of this compound:
- Pharmacological Potential: Quinoline derivatives are often investigated for their potential as antimicrobial, anticancer, and anti-inflammatory agents. 6-methyl-2-(3-pyridyl)quinoline-4-carboxylic acid may exhibit similar biological properties.
- Synthetic Applications: The compact structure of this compound enables it to serve as a valuable intermediate in the synthesis of more complex molecules. Researchers utilize it as a building block for developing novel compounds.
- Role in Coordination Chemistry: This compound can form coordination complexes with metals, enhancing its utility in catalysis and materials science. These metal complexes can display improved physical properties that make them suitable for various applications.
- Environmental Impact: Quinoline derivatives, including this compound, can serve as environmental indicators due to their stability and reactivity. They are often studied for their degradation products in ecological assessments.
- Multiple Functionalities: The presence of both carboxylic acid and pyridine groups in its structure opens doors to a variety of reactions, showcasing the multifaceted nature of this compound in chemical research.
In conclusion, the compound 6-methyl-2-(3-pyridyl)quinoline-4-carboxylic acid exemplifies the rich potential of quinoline-based compounds. As research unfolds, its applications may lead to significant advancements in medicinal chemistry, material science, and environmental studies.