L-Proline, 5-phenyl-, (5S)-, with the CAS number 917615-20-4, is a chiral amino acid derivative characterized by its unique structure, which includes a proline backbone with a phenyl group attached at the 5-position. This compound is notable for its role in various biochemical processes and potential applications in pharmaceuticals and materials science. As a proline derivative, it retains the cyclic structure typical of proline, contributing to its stability and ability to participate in peptide formation. The (5S) designation indicates the specific stereochemistry of the molecule, which is crucial for its biological activity and interactions. L-Proline derivatives are often studied for their influence on protein folding and stability, as well as their potential as building blocks in the synthesis of more complex organic compounds. Additionally, the presence of the phenyl group may enhance its hydrophobic interactions, influencing solubility and reactivity in various environments. Overall, L-Proline, 5-phenyl-, (5S)- is a compound of interest in both synthetic and biological chemistry.

L-Proline, 5-phenyl-, (5S)-

917615-20-4: L-Proline, 5-phenyl-, (5S)-, with the CAS number 917615-20-4, is a chiral amino acid derivative characterized by its unique structure, which includes a proline backbone with a phenyl group attached at the 5-position. This compound is notable for its role in various biochemical processes and potential applications in pharmaceuticals and materials science. As a proline derivative, it retains the cyclic structure typical of proline, contributing to its stability and ability to participate in peptide formation. The (5S) designation indicates the specific stereochemistry of the molecule, which is crucial for its biological activity and interactions. L-Proline derivatives are often studied for their influence on protein folding and stability, as well as their potential as building blocks in the synthesis of more complex organic compounds. Additionally, the presence of the phenyl group may enhance its hydrophobic interactions, influencing solubility and reactivity in various environments. Overall, L-Proline, 5-phenyl-, (5S)- is a compound of interest in both synthetic and biological chemistry.

(2S,5S)-5-Phenylpyrrolidine-2-Carboxylic Acid

(2S,5S)-5-Phenylpyrrolidine-2-carboxylic acid

CAS 917615-20-4

L-Proline, 5-phenyl-, (5S)-

(2S,5S)-5-Phenylpyrrolidine-2-Carboxylic Acid

Ref: IN-DA01BG09

(2S,5S)-5-Phenylpyrrolidine-2-carboxylic acid

Ref: 54-OR1033849

(2S,5S)-5-Phenylpyrrolidine-2-carboxylic acid

Ref: 10-F615844