Boc-D-His(3-Me)-OH, with the CAS number 200871-84-7, 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 the amino acid is in its D-enantiomer form, which is less common than the L-form typically found in proteins. The "His" refers to histidine, an amino acid known for its role in enzyme catalysis and metal ion coordination due to its imidazole side chain. The "(3-Me)" denotes a methyl group substitution at the third position of the imidazole ring, which can influence the compound's properties, such as solubility and reactivity. This compound is often utilized in peptide synthesis and research applications, particularly in studies involving histidine's role in biological systems. Its characteristics include stability under standard laboratory conditions, but it may require specific conditions for deprotection and further reactions.

Boc-D-His(3-Me)-OH

200871-84-7: Boc-D-His(3-Me)-OH, with the CAS number 200871-84-7, 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 the amino acid is in its D-enantiomer form, which is less common than the L-form typically found in proteins. The "His" refers to histidine, an amino acid known for its role in enzyme catalysis and metal ion coordination due to its imidazole side chain. The "(3-Me)" denotes a methyl group substitution at the third position of the imidazole ring, which can influence the compound's properties, such as solubility and reactivity. This compound is often utilized in peptide synthesis and research applications, particularly in studies involving histidine's role in biological systems. Its characteristics include stability under standard laboratory conditions, but it may require specific conditions for deprotection and further reactions.

CAS 200871-84-7

Boc-D-His(3-Me)-OH

Boc-D-His(3-Me)-OH

Ref: 01-4017899

Boc-D-His(3-Me)-OH

Ref: IN-DA002D2D

Boc-D-His(3-Me)-OH Boc-D His(p-Me)-OH

Ref: 54-OR36383

Boc-d-his(3-me)-oh

Ref: 10-F475407