Fmoc-D-Lys(Me,Boc)-OH

• CAT Number: L018376
• CAS Number: 2044709-77-3
• Molecular Formula: C27H34N2O6
• Molecular Weight: 482.60
• Purity: ≥95%
• IUPAC Name: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-6-[methyl-[(2-methylpropan-2-yl)oxycarbonyl]amino]hexanoic acid
• InChI: InChI=1S/C27H34N2O6/c1-27(2,3)35-26(33)29(4)16-10-9-15-23(24(30)31)28-25(32)34-17-22-20-13-7-5-11-18(20)19-12-6-8-14-21(19)22/h5-8,11-14,22-23H,9-10,15-17H2,1-4H3,(H,28,32)(H,30,31)/t23-/m1/s1
• InChIKey: JHMSFOFHTAYQLS-HSZRJFAPSA-N
• SMILES: CC(C)(C)OC(=O)N(C)CCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

Fmoc-D-Lys(Me,Boc)-OH（Cat No.:L018376）is a high-purity protected amino acid derivative commonly used in peptide synthesis and pharmaceutical research. This compound features a D-lysine residue with a methylated side chain and a Boc (tert-butoxycarbonyl) protecting group, along with an Fmoc (fluorenylmethyloxycarbonyl) group at the N-terminus. Its unique structure allows for selective incorporation into peptide sequences, facilitating the synthesis of complex peptides and proteins. Fmoc-D-Lys(Me,Boc)-OH is ideal for precise synthetic applications in medicinal chemistry, enabling the development of novel therapeutics and research in peptide science.