H-Lys(p-nitro-Z)-OH, also known as L-lysine p-nitrobenzyloxycarbonyl (Z) derivative, is a protected form of the amino acid lysine. This compound features a lysine backbone, which is characterized by its basic amino group and a carboxylic acid group, making it a polar and hydrophilic molecule. The "p-nitro" group indicates the presence of a nitro substituent on the aromatic ring, which can influence the compound's reactivity and solubility. The Z (benzyloxycarbonyl) protection is commonly used in peptide synthesis to prevent the amino group from participating in unwanted reactions, allowing for selective coupling with other amino acids. H-Lys(p-nitro-Z)-OH is typically utilized in the synthesis of peptides and proteins, particularly in solid-phase peptide synthesis, due to its stability and ease of removal of the protecting groups under specific conditions. The compound is soluble in organic solvents and exhibits characteristics typical of amino acids, such as the ability to form hydrogen bonds and participate in various chemical reactions.

H-Lys(p-nitro-Z)-OH

3557-90-2: H-Lys(p-nitro-Z)-OH, also known as L-lysine p-nitrobenzyloxycarbonyl (Z) derivative, is a protected form of the amino acid lysine. This compound features a lysine backbone, which is characterized by its basic amino group and a carboxylic acid group, making it a polar and hydrophilic molecule. The "p-nitro" group indicates the presence of a nitro substituent on the aromatic ring, which can influence the compound's reactivity and solubility. The Z (benzyloxycarbonyl) protection is commonly used in peptide synthesis to prevent the amino group from participating in unwanted reactions, allowing for selective coupling with other amino acids. H-Lys(p-nitro-Z)-OH is typically utilized in the synthesis of peptides and proteins, particularly in solid-phase peptide synthesis, due to its stability and ease of removal of the protecting groups under specific conditions. The compound is soluble in organic solvents and exhibits characteristics typical of amino acids, such as the ability to form hydrogen bonds and participate in various chemical reactions.

CAS 3557-90-2

H-Lys(p-nitro-Z)-OH

Ne-4-Nitro-Z-L-lysine

Ref: 10-F492925