(R)-2-methyl-1-((S)-1-phenylethyl)piperidin-4-one, with the CAS number 103539-61-3, is a chiral piperidinone derivative known for its potential applications in medicinal chemistry. This compound features a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and is substituted with a methyl group and a phenylethyl group, contributing to its stereochemical complexity. The presence of the chiral centers in both the piperidine and the phenylethyl moieties imparts specific stereochemical properties that can influence its biological activity and interaction with biological targets. Typically, such compounds may exhibit properties relevant to neurotransmitter modulation, making them of interest in the development of pharmaceuticals, particularly in the treatment of neurological disorders. The compound's solubility, stability, and reactivity can vary based on its stereochemistry and functional groups, which are critical for its potential therapeutic applications. Overall, (R)-2-methyl-1-((S)-1-phenylethyl)piperidin-4-one represents a significant structure in the field of organic and medicinal chemistry.

(R)-2-methyl-1-((s)-1-phenylethyl)piperidin-4-one

103539-61-3: (R)-2-methyl-1-((S)-1-phenylethyl)piperidin-4-one, with the CAS number 103539-61-3, is a chiral piperidinone derivative known for its potential applications in medicinal chemistry. This compound features a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and is substituted with a methyl group and a phenylethyl group, contributing to its stereochemical complexity. The presence of the chiral centers in both the piperidine and the phenylethyl moieties imparts specific stereochemical properties that can influence its biological activity and interaction with biological targets. Typically, such compounds may exhibit properties relevant to neurotransmitter modulation, making them of interest in the development of pharmaceuticals, particularly in the treatment of neurological disorders. The compound's solubility, stability, and reactivity can vary based on its stereochemistry and functional groups, which are critical for its potential therapeutic applications. Overall, (R)-2-methyl-1-((S)-1-phenylethyl)piperidin-4-one represents a significant structure in the field of organic and medicinal chemistry.

CAS 103539-61-3

(R)-2-methyl-1-((s)-1-phenylethyl)piperidin-4-one

(R)-2-Methyl-1-((S)-1-phenylethyl)piperidin-4-one

Ref: 10-F043029