Fmoc-D-His(Fmoc)-OH, with the CAS number 200926-18-7, is a protected derivative of the amino acid histidine, specifically designed for use in peptide synthesis. The "Fmoc" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective reactions during peptide assembly. This compound features a D-enantiomer of histidine, which is significant in studies involving peptide conformation and biological activity. The presence of two Fmoc groups indicates that it is a double-protected form, enhancing stability and preventing premature reactions. Fmoc-D-His(Fmoc)-OH is typically utilized in solid-phase peptide synthesis, where the Fmoc group can be easily removed under basic conditions, facilitating the sequential addition of amino acids. Its characteristics include good solubility in organic solvents, stability under standard laboratory conditions, and compatibility with various coupling reagents. This compound is valuable in the synthesis of peptides for research in biochemistry, pharmacology, and drug development, particularly in the study of histidine's role in biological systems.

Fmoc-D-His(Fmoc)-OH

200926-18-7: Fmoc-D-His(Fmoc)-OH, with the CAS number 200926-18-7, is a protected derivative of the amino acid histidine, specifically designed for use in peptide synthesis. The "Fmoc" (9-fluorenylmethoxycarbonyl) group serves as a protective group for the amino functionality, allowing for selective reactions during peptide assembly. This compound features a D-enantiomer of histidine, which is significant in studies involving peptide conformation and biological activity. The presence of two Fmoc groups indicates that it is a double-protected form, enhancing stability and preventing premature reactions. Fmoc-D-His(Fmoc)-OH is typically utilized in solid-phase peptide synthesis, where the Fmoc group can be easily removed under basic conditions, facilitating the sequential addition of amino acids. Its characteristics include good solubility in organic solvents, stability under standard laboratory conditions, and compatibility with various coupling reagents. This compound is valuable in the synthesis of peptides for research in biochemistry, pharmacology, and drug development, particularly in the study of histidine's role in biological systems.

D-Histidine, N,1-bis[(9H-fluoren-9-ylmethoxy)carbonyl]-

<p>(R)-3-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-1H-imidazol-4-yl)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoic acid</p>

CAS 200926-18-7

Fmoc-D-His(Fmoc)-OH

D-Histidine, N,1-bis[(9H-fluoren-9-ylmethoxy)carbonyl]-

Ref: IN-DA002D2T

(R)-3-(1-(((9H-Fluoren-9-yl)methoxy)carbonyl)-1H-imidazol-4-yl)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)propanoic acid

Ref: 54-OR1053452

N,1-Bis[(9H-fluoren-9-ylmethoxy)carbonyl]-D-histidine

Ref: 10-F771797