N-heptyl-L-hydroxyproline is an amino acid derivative characterized by its unique structure, which includes a heptyl side chain and a hydroxyproline moiety. This compound features a hydrophobic heptyl group, contributing to its lipophilicity, while the hydroxyproline component introduces a hydroxyl group that can participate in hydrogen bonding, enhancing its solubility in polar solvents. The presence of the proline structure imparts a cyclic conformation that can influence its biological activity and interactions with proteins. N-heptyl-L-hydroxyproline is of interest in various fields, including medicinal chemistry and biochemistry, due to its potential role in peptide synthesis and as a building block for more complex molecules. Its properties may also be explored in the context of drug design, particularly for compounds targeting specific biological pathways. As with many amino acid derivatives, the stereochemistry of N-heptyl-L-hydroxyproline is crucial for its biological function, making it a subject of interest in studies related to chirality and molecular recognition.

N-heptyl-L-hydroxyproline

76666-35-8: N-heptyl-L-hydroxyproline is an amino acid derivative characterized by its unique structure, which includes a heptyl side chain and a hydroxyproline moiety. This compound features a hydrophobic heptyl group, contributing to its lipophilicity, while the hydroxyproline component introduces a hydroxyl group that can participate in hydrogen bonding, enhancing its solubility in polar solvents. The presence of the proline structure imparts a cyclic conformation that can influence its biological activity and interactions with proteins. N-heptyl-L-hydroxyproline is of interest in various fields, including medicinal chemistry and biochemistry, due to its potential role in peptide synthesis and as a building block for more complex molecules. Its properties may also be explored in the context of drug design, particularly for compounds targeting specific biological pathways. As with many amino acid derivatives, the stereochemistry of N-heptyl-L-hydroxyproline is crucial for its biological function, making it a subject of interest in studies related to chirality and molecular recognition.

<p>The synthesis of N-heptyl-hyp-OH is a chiral resolution process for the preparation of the enantiomers of heptanol. The enantioselective synthesis of this compound is achieved by converting the racemic mixture to an optically active form by means of a chiral auxiliary, followed by protection and hydrolysis. This method produces an optically pure product in high yield.</p>

CAS 76666-35-8

N-heptyl-L-hydroxyproline

N-Heptyl-Hyp-OH

Ref: 3D-FH107884