7-Aminoquinoline-5-carboxylic acid is an organic compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. This compound features an amino group (-NH2) at the 7-position and a carboxylic acid group (-COOH) at the 5-position of the quinoline ring. These functional groups contribute to its polar nature, enhancing its solubility in polar solvents. The presence of the amino group allows for potential interactions in biological systems, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The carboxylic acid group can participate in acid-base reactions, influencing the compound's reactivity and stability. Additionally, 7-aminoquinoline-5-carboxylic acid may exhibit biological activity, including antimicrobial or antimalarial properties, due to its structural similarity to other biologically active quinoline derivatives. Its unique combination of functional groups and structural features makes it a valuable compound for research in various fields, including organic synthesis and drug development.

7-aminoquinoline-5-carboxylic acid

1956341-10-8: 7-Aminoquinoline-5-carboxylic acid is an organic compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. This compound features an amino group (-NH2) at the 7-position and a carboxylic acid group (-COOH) at the 5-position of the quinoline ring. These functional groups contribute to its polar nature, enhancing its solubility in polar solvents. The presence of the amino group allows for potential interactions in biological systems, making it of interest in medicinal chemistry, particularly in the development of pharmaceuticals. The carboxylic acid group can participate in acid-base reactions, influencing the compound's reactivity and stability. Additionally, 7-aminoquinoline-5-carboxylic acid may exhibit biological activity, including antimicrobial or antimalarial properties, due to its structural similarity to other biologically active quinoline derivatives. Its unique combination of functional groups and structural features makes it a valuable compound for research in various fields, including organic synthesis and drug development.

CAS 1956341-10-8

7-aminoquinoline-5-carboxylic acid

7-Aminoquinoline-5-carboxylic acid

Ref: IN-DA00I3GV

7-Aminoquinoline-5-carboxylic acid

Ref: 54-OR1068978

7-AMINOQUINOLINE-5-CARBOXYLIC ACID

Ref: 10-F501702