Fmoc-Dap(Z)-OH

• CAT Number: L026323
• CAS Number: 204316-36-9
• Molecular Formula: C26H24N2O6
• Molecular Weight: 460.50
• Purity: ≥95%
• IUPAC Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(phenylmethoxycarbonylamino)propanoic acid
• InChI: InChI=1S/C26H24N2O6/c29-24(30)23(14-27-25(31)33-15-17-8-2-1-3-9-17)28-26(32)34-16-22-20-12-6-4-10-18(20)19-11-5-7-13-21(19)22/h1-13,22-23H,14-16H2,(H,27,31)(H,28,32)(H,29,30)/t23-/m0/s1
• InChIKey: CDAHZCMBWKGJEC-QHCPKHFHSA-N
• SMILES: C1=CC=C(C=C1)COC(=O)NC[C@@H](C(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24

Fmoc-Dap(Z)-OH（Cat No.:L026323）is a protected amino acid derivative used in peptide synthesis. It consists of Fmoc (9-fluorenylmethoxycarbonyl) as a protecting group on the amino group of 2,4-diaminopimelic acid (Dap), with a Z (benzyloxycarbonyl) protection on the ε-amino group. This compound is utilized in solid-phase peptide synthesis (SPPS) to ensure selective deprotection of the Fmoc group and allow for sequential peptide chain elongation. The Z-protection on the side chain amino group ensures stability and prevents undesired reactions. It is widely used for synthesizing peptides that require precise functional group control.