CAS 96201-52-4

2-(biphenyl-4-yl)-5-chloro-3-methylquinoline-4-carboxylic acid

Description:

2-(Biphenyl-4-yl)-5-chloro-3-methylquinoline-4-carboxylic acid is a chemical compound characterized by its complex structure, which includes a quinoline core substituted with a biphenyl group and a carboxylic acid functional group. This compound typically exhibits properties associated with both aromatic and heterocyclic compounds, such as stability and potential for π-π stacking interactions due to its extended conjugated system. The presence of the chlorine atom introduces additional reactivity and can influence the compound's solubility and biological activity. As a carboxylic acid, it can participate in acid-base reactions and may form salts or esters. The compound's unique structure suggests potential applications in pharmaceuticals, particularly in the development of biologically active molecules, as quinoline derivatives are known for their diverse biological activities, including antimicrobial and anticancer properties. Its specific characteristics, such as melting point, solubility, and spectral data, would typically be determined through experimental methods and may vary based on the conditions of synthesis and purification.

Formula: C₂₃H₁₆ClNO₂

InChI: InChI=1/C23H16ClNO2/c1-14-20(23(26)27)21-18(24)8-5-9-19(21)25-22(14)17-12-10-16(11-13-17)15-6-3-2-4-7-15/h2-13H,1H3,(H,26,27)

Synonyms:

• 4-quinolinecarboxylic acid, 2-[1,1'-biphenyl]-4-yl-5-chloro-3-methyl-

S 8660

CAS: 96201-52-4

S 8660 is an analogue of brequinar sodium that inhibits the pyrimidine biosynthetic pathway.

Formula: C₂₃H₁₆ClNO₂

Color and Shape: Solid

Molecular weight: 373.83

Ref: TM-T68218