5,7-Dichloro-4-oxo-1H-quinoline-2-carboxylic acid
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- Molecular formula
- C10H4Cl2NO3
- CAS Number
- 84087-01-4
- IUPAC Name
- 5,7-dichloro-4-oxo-1H-quinoline-2-carboxylic acid
- Molecular Weight
- 286.05g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.7000g/cm3
- Synonyms
- 5, 7-Dichlorokynurenic acid
Identification
Interesting facts
Interesting Facts About 5,7-Dichloro-4-oxo-1H-quinoline-2-carboxylic Acid
5,7-Dichloro-4-oxo-1H-quinoline-2-carboxylic acid is a fascinating compound that falls within the quinoline family, known for its diverse applications and biological properties. Here are some important points and intriguing facts about this compound:
- Quinoline Derivative: The compound is a derivative of quinoline, which is a nitrogen-containing heterocyclic aromatic organic compound. Quinoline and its derivatives have been extensively studied for their antibacterial, antifungal, and anti-inflammatory activities.
- Chlorine Atoms: The presence of two chlorine atoms (dihalo substitution) enhances the compound's biological activity. Chlorine is often employed in medicinal chemistry to improve the pharmacokinetic properties of pharmaceuticals.
- Biological Activity: Compounds related to 5,7-dichloro-4-oxo-1H-quinoline-2-carboxylic acid have shown promise in *antimicrobial* and *antiviral* agents. This highlights the potential applicability of the compound in drug development.
- Structure-Activity Relationship (SAR): Researchers often investigate the structure-activity relationship of such compounds to understand how changes in structure affect biological activity. The incorporation of various functional groups can significantly alter the compound's effects.
- Research Applications: Its utility in research is notable, particularly in studying various biochemical pathways and mechanisms. It can also serve as a building block for synthesizing more complex molecules and pharmaceuticals.
- Environmental Aspect: As with many synthetic compounds, understanding the environmental impact of 5,7-dichloro-4-oxo-1H-quinoline-2-carboxylic acid is crucial. Studies on its stability and degradation in environmental samples are essential to assess its ecological footprint.
In conclusion, the compound 5,7-dichloro-4-oxo-1H-quinoline-2-carboxylic acid is a promising subject of study due to its unique structure and potential applications in medicinal chemistry. Continuous research could unravel further insights into its properties and uses, making it a noteworthy compound in the field of chemistry.