CAS 210755-31-0: FMOC-D-HIS(BOC)-OH CHA

Description: FMOC-D-HIS(BOC)-OH CHA is a chemical compound commonly used in peptide synthesis and research. It is a derivative of histidine, an essential amino acid, and features a fluorenylmethyloxycarbonyl (FMOC) protecting group, which is widely utilized to protect amino groups during peptide synthesis. The BOC (tert-butyloxycarbonyl) group further protects the side chain of the histidine residue, enhancing stability and preventing unwanted reactions. This compound is typically characterized by its solid state, and it is soluble in organic solvents such as dimethylformamide (DMF) and dimethyl sulfoxide (DMSO), but less soluble in water. Its molecular structure allows for selective deprotection under mild conditions, making it valuable in the synthesis of complex peptides and proteins. The presence of the histidine moiety contributes to the compound's ability to participate in metal coordination and catalysis, which is significant in biochemical applications. Overall, FMOC-D-HIS(BOC)-OH CHA is an important reagent in the field of organic and medicinal chemistry.

Synonyms:

• Fmoc-N-Im-Boc-D-Histidine Cyclohexylammonium Salt
• N-Alpha-Fmoc-N-Im-T-Boc-D-Histidine Cyclohexylammonium Salt
• Fmoc-D-His(Boc)-OH・CHA

D-Histidine, 1-[(1,1-dimethylethoxy)carbonyl]-N-[(9H-fluoren-9-ylmethoxy)carbonyl]-, compd. with cyclohexanamine (1:1) (9CI)

CAS: 210755-31-0

• Formula: C₃₂H₄₀N₄O₆
• Purity: 98%
• Molecular weight: 576.6832

N-α-Fmoc-Nim-Boc-D-histidine cyclohexylammonium salt

CAS: 210755-31-0

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• Formula: C₃₂H₄₀N₄O₆
• Purity: Min. 95%
• Molecular weight: 576.68 g/mol