L-Proline, 5-phenyl-, (5R)-, with the CAS number 203645-40-3, is an amino acid derivative characterized by its unique structure that includes a proline backbone with a phenyl group attached at the 5-position. This compound is a chiral molecule, exhibiting optical activity due to the presence of a stereocenter, which is indicated by the (5R) designation. L-Proline itself is a non-essential amino acid, playing a crucial role in protein synthesis and serving as a building block for various peptides. The phenyl substitution enhances its hydrophobic characteristics, potentially influencing its interactions in biological systems. This compound may be utilized in various applications, including pharmaceuticals, where it can serve as a precursor or intermediate in the synthesis of bioactive molecules. Additionally, its structural properties may contribute to its function in biochemical pathways, particularly in the stabilization of protein structures and in the modulation of enzyme activity. Overall, L-Proline, 5-phenyl-, (5R)- is of interest in both research and industrial contexts due to its unique chemical properties and biological relevance.

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

203645-40-3: L-Proline, 5-phenyl-, (5R)-, with the CAS number 203645-40-3, is an amino acid derivative characterized by its unique structure that includes a proline backbone with a phenyl group attached at the 5-position. This compound is a chiral molecule, exhibiting optical activity due to the presence of a stereocenter, which is indicated by the (5R) designation. L-Proline itself is a non-essential amino acid, playing a crucial role in protein synthesis and serving as a building block for various peptides. The phenyl substitution enhances its hydrophobic characteristics, potentially influencing its interactions in biological systems. This compound may be utilized in various applications, including pharmaceuticals, where it can serve as a precursor or intermediate in the synthesis of bioactive molecules. Additionally, its structural properties may contribute to its function in biochemical pathways, particularly in the stabilization of protein structures and in the modulation of enzyme activity. Overall, L-Proline, 5-phenyl-, (5R)- is of interest in both research and industrial contexts due to its unique chemical properties and biological relevance.

CAS 203645-40-3

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

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

Ref: IN-DA00292C