Rel-Phenylmethyl (3R,4S)-3-fluoro-4-hydroxy-4-methyl-1-piperidinecarboxylate is a chemical compound characterized by its specific stereochemistry and functional groups. It features a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and includes a carboxylate group that contributes to its potential as a bioactive molecule. The presence of a fluorine atom at the 3-position and a hydroxyl group at the 4-position indicates that this compound may exhibit unique reactivity and biological activity, possibly influencing its pharmacological properties. The methyl group at the 4-position further adds to its steric and electronic characteristics. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that could interact with biological targets. Its specific stereochemistry (3R,4S) suggests that it may have distinct enantiomeric properties, which can significantly affect its efficacy and safety in biological systems. As with many compounds, its solubility, stability, and reactivity would depend on the surrounding conditions and the presence of other functional groups.

rel-Phenylmethyl (3R,4S)-3-fluoro-4-hydroxy-4-methyl-1-piperidinecarboxylate

1612176-01-8: Rel-Phenylmethyl (3R,4S)-3-fluoro-4-hydroxy-4-methyl-1-piperidinecarboxylate is a chemical compound characterized by its specific stereochemistry and functional groups. It features a piperidine ring, which is a six-membered nitrogen-containing heterocycle, and includes a carboxylate group that contributes to its potential as a bioactive molecule. The presence of a fluorine atom at the 3-position and a hydroxyl group at the 4-position indicates that this compound may exhibit unique reactivity and biological activity, possibly influencing its pharmacological properties. The methyl group at the 4-position further adds to its steric and electronic characteristics. This compound may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that could interact with biological targets. Its specific stereochemistry (3R,4S) suggests that it may have distinct enantiomeric properties, which can significantly affect its efficacy and safety in biological systems. As with many compounds, its solubility, stability, and reactivity would depend on the surrounding conditions and the presence of other functional groups.

CAS 1612176-01-8

rel-Phenylmethyl (3R,4S)-3-fluoro-4-hydroxy-4-methyl-1-piperidinecarboxylate

Trans-Benzyl 3-Fluoro-4-Hydroxy-4-Methylpiperidine-1-Carboxylate

Ref: IN-DA00HYNI