FMOC-D-ORN(BOC)-OH

• CAT Number: M019318
• CAS Number: 118476-89-4
• Molecular Formula: C25H30N2O6
• Molecular Weight: 454.52
• Purity: ≥95%
• Storage: Store at +4C
• IUPAC Name: (2R)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-5-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoic acid
• InChI: InChI=1S/C25H30N2O6/c1-25(2,3)33-23(30)26-14-8-13-21(22(28)29)27-24(31)32-15-20-18-11-6-4-9-16(18)17-10-5-7-12-19(17)20/h4-7,9-12,20-21H,8,13-15H2,1-3H3,(H,26,30)(H,27,31)(H,28,29)/t21-/m1/s1
• InChIKey: JOOIZTMAHNLNHE-OAQYLSRUSA-N
• SMILES: CC(C)(C)OC(=O)NCCCC(C(=O)O)NC(=O)OCC1C2=CC=CC=C2C3=CC=CC=C13

Fmoc-D-Orn(Boc)-OH (Cat No.: M019318) is a protected amino acid derivative used in solid-phase peptide synthesis (SPPS). It features a D-ornithine backbone with an Fmoc (9-fluorenylmethyloxycarbonyl) group protecting the α-amino group and a Boc (tert-butoxycarbonyl) group protecting the δ-amino side chain. This dual-protected form ensures orthogonal deprotection during stepwise peptide assembly, allowing selective functionalization. Fmoc-D-Orn(Boc)-OH is especially useful in designing peptides with non-natural stereochemistry, enhancing protease resistance and modulating biological activity in pharmaceutical and biochemical research applications.