Boc-D-His(1-Me)-OH, with the CAS number 200871-52-9, is a protected derivative of the amino acid histidine. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, facilitating the synthesis of peptides by preventing unwanted reactions during coupling processes. The "D" indicates that this compound is the D-enantiomer of histidine, which is important in specific biochemical contexts. The "1-Me" denotes a methyl group attached to the nitrogen of the imidazole ring, which can influence the compound's properties, such as solubility and reactivity. This compound is typically used in peptide synthesis and research involving histidine derivatives, as it retains the essential characteristics of histidine while providing stability and ease of handling. Its solubility in organic solvents and its ability to participate in various chemical reactions make it a valuable intermediate in the synthesis of more complex molecules. Overall, Boc-D-His(1-Me)-OH is significant in the field of medicinal chemistry and peptide research.

Boc-D-His(1-Me)-OH

200871-52-9: Boc-D-His(1-Me)-OH, with the CAS number 200871-52-9, is a protected derivative of the amino acid histidine. The "Boc" (tert-butyloxycarbonyl) group serves as a protective group for the amino functionality, facilitating the synthesis of peptides by preventing unwanted reactions during coupling processes. The "D" indicates that this compound is the D-enantiomer of histidine, which is important in specific biochemical contexts. The "1-Me" denotes a methyl group attached to the nitrogen of the imidazole ring, which can influence the compound's properties, such as solubility and reactivity. This compound is typically used in peptide synthesis and research involving histidine derivatives, as it retains the essential characteristics of histidine while providing stability and ease of handling. Its solubility in organic solvents and its ability to participate in various chemical reactions make it a valuable intermediate in the synthesis of more complex molecules. Overall, Boc-D-His(1-Me)-OH is significant in the field of medicinal chemistry and peptide research.

CAS 200871-52-9

Boc-D-His(1-Me)-OH

Boc-D-His(1-Me)-OH

Ref: 01-4026737

Boc-D-His(1-Me)-OH Boc-D-His(t-Me)-OH

Ref: 54-OR36384