3-[(2-Methylpiperidin-1-yl)methyl]aniline, with the CAS number 937669-68-6, is an organic compound characterized by its amine functional group and a piperidine ring. This compound features a phenyl group attached to an aniline structure, which is further substituted with a 2-methylpiperidin-1-ylmethyl group. The presence of the piperidine ring contributes to its potential as a pharmacophore in medicinal chemistry, often enhancing solubility and bioavailability. The compound is likely to exhibit basic properties due to the amine group, making it capable of forming salts with acids. Its molecular structure suggests potential applications in drug development, particularly in areas targeting central nervous system disorders, given the piperidine's known activity in various therapeutic contexts. Additionally, the compound's stability and reactivity can be influenced by the substituents on the aromatic ring and the piperidine, which may affect its interaction with biological targets. Overall, 3-[(2-methylpiperidin-1-yl)methyl]aniline represents a versatile scaffold for further chemical modifications and investigations in pharmaceutical research.

3-[(2-methylpiperidin-1-yl)methyl]aniline

937669-68-6: 3-[(2-Methylpiperidin-1-yl)methyl]aniline, with the CAS number 937669-68-6, is an organic compound characterized by its amine functional group and a piperidine ring. This compound features a phenyl group attached to an aniline structure, which is further substituted with a 2-methylpiperidin-1-ylmethyl group. The presence of the piperidine ring contributes to its potential as a pharmacophore in medicinal chemistry, often enhancing solubility and bioavailability. The compound is likely to exhibit basic properties due to the amine group, making it capable of forming salts with acids. Its molecular structure suggests potential applications in drug development, particularly in areas targeting central nervous system disorders, given the piperidine's known activity in various therapeutic contexts. Additionally, the compound's stability and reactivity can be influenced by the substituents on the aromatic ring and the piperidine, which may affect its interaction with biological targets. Overall, 3-[(2-methylpiperidin-1-yl)methyl]aniline represents a versatile scaffold for further chemical modifications and investigations in pharmaceutical research.

CAS 937669-68-6

3-[(2-methylpiperidin-1-yl)methyl]aniline

3-[(2-methyl-1-piperidinyl)methyl]aniline

Ref: 10-F311032