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CAS 89391-05-9

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2-(1H-Indol-3-yl)-6-methyl-4-quinolinecarboxylic acid

Description:
2-(1H-Indol-3-yl)-6-methyl-4-quinolinecarboxylic acid, with the CAS number 89391-05-9, is a chemical compound that features a complex structure combining indole and quinoline moieties. This compound typically exhibits characteristics such as being a solid at room temperature, with potential applications in medicinal chemistry due to its bioactive properties. The presence of both indole and quinoline rings suggests that it may possess interesting pharmacological activities, including antimicrobial, anti-inflammatory, or anticancer effects, although specific biological activities would need to be confirmed through empirical studies. The carboxylic acid functional group contributes to its acidity and solubility in polar solvents, which can influence its reactivity and interaction with biological targets. Additionally, the methyl group at the 6-position of the quinoline ring may affect the compound's steric and electronic properties, potentially enhancing its biological activity or selectivity. Overall, this compound represents a valuable scaffold for further research in drug development and organic synthesis.
Formula:C19H14N2O2
InChI:InChI=1S/C19H14N2O2/c1-11-6-7-17-13(8-11)14(19(22)23)9-18(21-17)15-10-20-16-5-3-2-4-12(15)16/h2-10,20H,1H3,(H,22,23)
InChI key:InChIKey=QFRYAJKOOTXZPO-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=CC(C=2C=3C(NC2)=CC=CC3)=NC4=C1C=C(C)C=C4
Synonyms:
  • 2-(1H-Indol-3-yl)-6-methyl-4-quinolinecarboxylic acid
  • 2-Indol-3-yl-6-methyl-quinoline-4-carboxylic acid
  • 4-Quinolinecarboxylic acid, 2-(1H-indol-3-yl)-6-methyl-
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