Fmoc-D-Lys(Boc)-OH
$250.00
CAS No.: 92122-45-7
Catalog No.: 195291
Purity: 95%
MF: C26H32N2O6
MW: 468.55
Storage: 2-8 degree Celsius
SMILES: C1=CC=CC=2C3=CC=CC=C3C(C12)COC(=O)N[C@H](CCCCNC(=O)OC(C)(C)C)C(=O)O
Catalog No.: 195291
Purity: 95%
MF: C26H32N2O6
MW: 468.55
Storage: 2-8 degree Celsius
SMILES: C1=CC=CC=2C3=CC=CC=C3C(C12)COC(=O)N[C@H](CCCCNC(=O)OC(C)(C)C)C(=O)O
Fmoc-D-Lys(Boc)-OH; N2-(((9H-fluoren-9-yl)methoxy)carbonyl)-N6-(tert-butoxycarbonyl)-D-lysine; CAS No.: 92122-45-7; Fmoc-D-Lys(Boc)-OH. PROPERTIES: Fmoc-D-Lys(Boc)-OH is a protected amino acid derivative used in peptide synthesis. This compound has a molecular weight of 417.48 g/mol and appears as a white to off-white solid. It demonstrates limited water solubility but dissolves in common organic solvents. Fmoc-D-Lys(Boc)-OH should be stored at room temperature in a dry, dark environment. It is sensitive to moisture and light. Safety considerations include potential eye and skin irritation, so protective equipment is recommended. APPLICATIONS: Fmoc-D-Lys(Boc)-OH serves as a monomer in the synthesis of peptides containing D-lysine residues with Boc protection on the side chain amino group. In medicinal chemistry, it is used to create peptidomimetics with enhanced stability. In research applications, Fmoc-D-Lys(Boc)-OH facilitates the preparation of peptides for studying conformational effects on bioactivity and enzyme recognition. These applications are referenced in peptide synthesis protocols and medicinal chemistry literature.
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