3-(2-Methylpiperidin-1-yl)propanoic acid is an organic compound characterized by its structure, which includes a propanoic acid moiety attached to a 2-methylpiperidine ring. This compound features a carboxylic acid functional group (-COOH), which imparts acidic properties, allowing it to participate in various chemical reactions, such as esterification and amidation. The presence of the piperidine ring contributes to its potential as a pharmacophore in medicinal chemistry, as piperidine derivatives are often associated with biological activity. The compound is likely to be a white to off-white solid at room temperature and may exhibit moderate solubility in polar solvents due to the hydrophilic nature of the carboxylic acid group. Its molecular structure suggests that it could engage in hydrogen bonding, influencing its physical properties and reactivity. Additionally, the presence of the methyl group on the piperidine ring may affect its steric and electronic properties, potentially impacting its interactions in biological systems. Overall, this compound may have applications in drug development and synthesis.

3-(2-methylpiperidin-1-yl)propanoic acid

773108-59-1: 3-(2-Methylpiperidin-1-yl)propanoic acid is an organic compound characterized by its structure, which includes a propanoic acid moiety attached to a 2-methylpiperidine ring. This compound features a carboxylic acid functional group (-COOH), which imparts acidic properties, allowing it to participate in various chemical reactions, such as esterification and amidation. The presence of the piperidine ring contributes to its potential as a pharmacophore in medicinal chemistry, as piperidine derivatives are often associated with biological activity. The compound is likely to be a white to off-white solid at room temperature and may exhibit moderate solubility in polar solvents due to the hydrophilic nature of the carboxylic acid group. Its molecular structure suggests that it could engage in hydrogen bonding, influencing its physical properties and reactivity. Additionally, the presence of the methyl group on the piperidine ring may affect its steric and electronic properties, potentially impacting its interactions in biological systems. Overall, this compound may have applications in drug development and synthesis.

CAS 773108-59-1

3-(2-methylpiperidin-1-yl)propanoic acid

3-(2-Methylpiperidin-1-yl)propanoic acid

Ref: 54-OR1064417