Pyrrolidine, 3-phenyl-, (S)-, with the CAS number 62624-46-8, is a chiral compound characterized by its pyrrolidine ring, which is a five-membered saturated heterocyclic structure containing one nitrogen atom. The presence of the phenyl group at the third position of the pyrrolidine ring contributes to its unique properties, including its potential as a building block in organic synthesis and pharmaceutical applications. As an enantiomer, the (S)- configuration indicates that it has specific stereochemical properties, which can influence its biological activity and interactions. This compound is typically colorless to pale yellow and may exhibit solubility in organic solvents. Its reactivity can be attributed to the nitrogen atom, which can participate in various chemical reactions, including nucleophilic substitutions and ring-opening reactions. The compound's characteristics make it of interest in medicinal chemistry, particularly in the development of drugs targeting the central nervous system or other therapeutic areas. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

Pyrrolidine, 3-phenyl-, (S)-

62624-46-8: Pyrrolidine, 3-phenyl-, (S)-, with the CAS number 62624-46-8, is a chiral compound characterized by its pyrrolidine ring, which is a five-membered saturated heterocyclic structure containing one nitrogen atom. The presence of the phenyl group at the third position of the pyrrolidine ring contributes to its unique properties, including its potential as a building block in organic synthesis and pharmaceutical applications. As an enantiomer, the (S)- configuration indicates that it has specific stereochemical properties, which can influence its biological activity and interactions. This compound is typically colorless to pale yellow and may exhibit solubility in organic solvents. Its reactivity can be attributed to the nitrogen atom, which can participate in various chemical reactions, including nucleophilic substitutions and ring-opening reactions. The compound's characteristics make it of interest in medicinal chemistry, particularly in the development of drugs targeting the central nervous system or other therapeutic areas. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

CAS 62624-46-8

Pyrrolidine, 3-phenyl-, (S)-

(S)-3-phenylpyrrolidine

Ref: IN-DA00F5G3

(3S)-3-Phenylpyrrolidine

Ref: 54-OR924732

(3S)-3-PHENYLPYRROLIDINE

Ref: 10-F502884