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CAS 218156-60-6

:

6-chloro-8-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Description:
6-Chloro-8-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid is a synthetic organic compound belonging to the class of quinolines, which are bicyclic aromatic compounds. This substance features a chloro substituent at the 6-position and a methyl group at the 8-position, contributing to its unique chemical properties. The presence of a carboxylic acid functional group at the 3-position enhances its acidity and solubility in polar solvents. The compound exhibits potential biological activity, making it of interest in medicinal chemistry, particularly for its possible antibacterial or antifungal properties. Its structure includes a diketone moiety, which may participate in various chemical reactions, such as condensation or cyclization. The compound's stability and reactivity can be influenced by the electron-withdrawing effects of the chloro group and the electron-donating effects of the methyl group. Overall, 6-chloro-8-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid is a versatile compound with potential applications in pharmaceuticals and organic synthesis.
Formula:C11H8ClNO3
InChI:InChI=1/C11H8ClNO3/c1-5-2-6(12)3-7-9(5)13-4-8(10(7)14)11(15)16/h2-4H,1H3,(H,13,14)(H,15,16)
SMILES:Cc1cc(cc2c1[nH]cc(c2=O)C(=O)O)Cl
Synonyms:
  • 3-Quinolinecarboxylic acid, 6-chloro-1,4-dihydro-8-methyl-4-oxo-
  • 3-Quinolinecarboxylic acid, 6-chloro-4-hydroxy-8-methyl-
  • 6-Chloro-1,4-dihydro-8-methyl-4-oxo-3-quinolinecarboxylic acid
  • 6-Chloro-4-hydroxy-8-methylquinoline-3-carboxylic acid
  • T66 Bm Evj Dvq Hg J1
  • T66 Bnj Dvq Eq Hg J1
  • 6-Chloro-8-methyl-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
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