Z-D-allo-Ile-OH, also known as Z-D-allo-isoleucine hydroxylamine, is a chemical compound characterized by its structure as a derivative of the amino acid isoleucine. The "Z" prefix indicates the presence of a benzyloxycarbonyl (Z) protecting group, which is commonly used in peptide synthesis to protect the amino group. The "D" signifies that the isomer is in the D-form, which is the enantiomer of the naturally occurring L-isoleucine. The hydroxyl group (-OH) suggests that this compound may participate in hydrogen bonding, influencing its solubility and reactivity. The presence of DCHA (dihydrochloride salt) indicates that the compound is in a salt form, which can enhance its stability and solubility in various solvents. This compound is often utilized in biochemical research and peptide synthesis due to its specific stereochemistry and functional groups, making it valuable for studying protein interactions and enzymatic processes. As with many amino acid derivatives, its properties can be influenced by pH, temperature, and the presence of other chemical species.

Z-D-allo-Ile-OH . DCHA

55723-45-0: Z-D-allo-Ile-OH, also known as Z-D-allo-isoleucine hydroxylamine, is a chemical compound characterized by its structure as a derivative of the amino acid isoleucine. The "Z" prefix indicates the presence of a benzyloxycarbonyl (Z) protecting group, which is commonly used in peptide synthesis to protect the amino group. The "D" signifies that the isomer is in the D-form, which is the enantiomer of the naturally occurring L-isoleucine. The hydroxyl group (-OH) suggests that this compound may participate in hydrogen bonding, influencing its solubility and reactivity. The presence of DCHA (dihydrochloride salt) indicates that the compound is in a salt form, which can enhance its stability and solubility in various solvents. This compound is often utilized in biochemical research and peptide synthesis due to its specific stereochemistry and functional groups, making it valuable for studying protein interactions and enzymatic processes. As with many amino acid derivatives, its properties can be influenced by pH, temperature, and the presence of other chemical species.

CAS 55723-45-0

Z-D-allo-Ile-OH . DCHA

D-Alloisoleucine, N-[(phenylmethoxy)carbonyl]-

Ref: IN-DA00I9XU

Cbz-D-Allo-Isoleucine

Ref: 54-OR1012628

Benzyloxycarbonyl-D-alloisoleucine

Ref: 10-F986695