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CAS 35973-14-9

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6-Chloro-4-hydroxyquinoline-3-carboxylic acid

Description:
6-Chloro-4-hydroxyquinoline-3-carboxylic acid is an organic compound characterized by its quinoline structure, which features a chlorine atom and a hydroxyl group at specific positions on the ring. This compound typically exhibits properties such as being a solid at room temperature, with potential solubility in polar solvents due to the presence of the carboxylic acid and hydroxyl functional groups. It may display acidic behavior due to the carboxylic acid group, allowing it to participate in various chemical reactions, including esterification and amidation. The chlorine substituent can influence the compound's reactivity and biological activity, making it of interest in medicinal chemistry and research. Additionally, its structural features may contribute to its potential applications in pharmaceuticals, agrochemicals, or as a biochemical probe. The compound's stability, reactivity, and interaction with biological systems are influenced by its molecular structure, making it a subject of study in various chemical and biological contexts.
Formula:C10H6ClNO3
InChI:InChI=1/C10H6ClNO3/c11-5-1-2-8-6(3-5)9(13)7(4-12-8)10(14)15/h1-4H,(H,12,13)(H,14,15)
SMILES:c1cc2c(cc1Cl)c(=O)c(c[nH]2)C(=O)O
Synonyms:
  • 6-Chloro-4-Oxo-1,4-Dihydroquinoline-3-Carboxylic Acid
  • 4-Hydroxy-6-chloroquinoline-3-carboxylic acid
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