CAS 136871-75-5

3-Piperidinamine, 2-phenyl-, (2S,3S)-

Description:

3-Piperidinamine, 2-phenyl-, (2S,3S)-, also known by its CAS number 136871-75-5, is a chiral organic compound characterized by its piperidine ring structure, which is a six-membered nitrogen-containing heterocycle. This compound features a phenyl group attached to the second carbon of the piperidine ring and an amine functional group at the third carbon, contributing to its basicity and potential reactivity. The (2S,3S) designation indicates its specific stereochemistry, which can influence its biological activity and interactions with other molecules. Typically, such compounds may exhibit properties relevant to medicinal chemistry, including potential applications in drug development due to their ability to interact with biological targets. The presence of both a piperidine and a phenyl group suggests that it may have lipophilic characteristics, which can affect its solubility and permeability in biological systems. Overall, the unique structural features of 3-Piperidinamine, 2-phenyl-, (2S,3S)- make it a compound of interest in various chemical and pharmaceutical research contexts.

Formula: C₁₁H₁₆N₂

(2S,3S)-(-)-3-Amino-2-phenylpiperidine

CAS: 136871-75-5

The process of asymmetric epoxidation is used to convert alkenes into epoxides in a single step. This reaction is catalyzed by the use of a chiral catalyst with an enantiomeric excess (ee) greater than 50%. The reactants are added to the catalyst and hydrogen peroxide, which oxidizes the alkenes. The resulting epoxides can be isolated from the reaction mixture by distillation or extraction. Factors that affect this reaction include the type of reactant, solvent, temperature, and pressure.

Formula: C₁₁H₁₆N₂

Purity: Min. 95%

Molecular weight: 176.26 g/mol

Ref: 3D-FA166489