Piperidine, 3-methyl-, (3R)- is a chiral amine characterized by its six-membered ring structure containing five carbon atoms and one nitrogen atom. The specific configuration at the third carbon (3R) indicates that it has a particular stereochemistry, which can influence its reactivity and interactions in biological systems. This compound is a derivative of piperidine, a saturated heterocyclic compound commonly used as a building block in organic synthesis and pharmaceuticals. The presence of the methyl group at the third position can affect the compound's physical properties, such as boiling point and solubility, as well as its biological activity. Piperidine derivatives are often explored for their potential applications in medicinal chemistry, particularly in the development of drugs targeting various neurological and psychiatric conditions. Additionally, the compound may exhibit basic properties due to the nitrogen atom, allowing it to participate in various chemical reactions, including alkylation and acylation. Overall, Piperidine, 3-methyl-, (3R)- is significant in both synthetic and medicinal chemistry contexts.

Piperidine, 3-methyl-, (3R)-

16078-25-4: Piperidine, 3-methyl-, (3R)- is a chiral amine characterized by its six-membered ring structure containing five carbon atoms and one nitrogen atom. The specific configuration at the third carbon (3R) indicates that it has a particular stereochemistry, which can influence its reactivity and interactions in biological systems. This compound is a derivative of piperidine, a saturated heterocyclic compound commonly used as a building block in organic synthesis and pharmaceuticals. The presence of the methyl group at the third position can affect the compound's physical properties, such as boiling point and solubility, as well as its biological activity. Piperidine derivatives are often explored for their potential applications in medicinal chemistry, particularly in the development of drugs targeting various neurological and psychiatric conditions. Additionally, the compound may exhibit basic properties due to the nitrogen atom, allowing it to participate in various chemical reactions, including alkylation and acylation. Overall, Piperidine, 3-methyl-, (3R)- is significant in both synthetic and medicinal chemistry contexts.

CAS 16078-25-4

Piperidine, 3-methyl-, (3R)-

Piperidine, 3-methyl-, (3R)-

Ref: IN-DA001VCH

(R)-3-Methyl-piperidine

Ref: 10-F095326