CAS 139051-78-8: trans-2-Carboxy-5,7-dichloro-4-phenylaminocarbonyl amino-1,2,3,4-tetrahydroquinoline

Description:Trans-2-Carboxy-5,7-dichloro-4-phenylaminocarbonyl amino-1,2,3,4-tetrahydroquinoline is a complex organic compound characterized by its multi-functional groups and a bicyclic structure. The presence of a carboxylic acid group (-COOH) indicates potential acidity and reactivity, while the dichloro substituents suggest enhanced biological activity or specificity in interactions, possibly influencing its pharmacological properties. The phenylamino group contributes to the compound's ability to engage in π-π stacking interactions, which can be significant in biological systems. The tetrahydroquinoline framework provides a rigid structure that may affect the compound's conformation and, consequently, its reactivity and binding affinity to biological targets. This compound may exhibit various properties, including solubility in organic solvents, potential for hydrogen bonding due to the amino and carboxylic acid groups, and possible applications in medicinal chemistry, particularly in the development of pharmaceuticals. Its specific characteristics, such as melting point, boiling point, and spectral data, would require empirical measurement or literature reference for precise values.

Formula:C₁₇H₁₅Cl₂N₃O₃

InChI:InChI=1/C17H15Cl2N3O3/c18-9-6-11(19)15-12(7-9)21-14(16(23)24)8-13(15)22-17(25)20-10-4-2-1-3-5-10/h1-7,13-14,21H,8H2,(H,23,24)(H2,20,22,25)/t13-,14+/m0/s1

Synonyms:
L 689560
4-trans-2-Carboxy-5,7-dichloro-4-phenylaminocarbonylamino-1,2,3,4-tetrahydroquinoline
trans-2-Carboxy-5,7-dichloro-4-(((phenylamino)carbonyl)amino)-1,2,3,4-tetrahydroquinoline
2-Quinolinecarboxylic acid, 5,7-dichloro-1,2,3,4-tetrahydro-4-(((phenylamino)carbonyl)amino)-, trans-(+-)-
(2S,4R)-5,7-dichloro-4-[(phenylcarbamoyl)amino]-1,2,3,4-tetrahydroquinoline-2-carboxylic acid
(2R,4S)-5,7-dichloro-4-[(phenylcarbamoyl)amino]-1,2,3,4-tetrahydroquinoline-2-carboxylic acid