Fmoc-R-3-amino-4-(3,5-difluorophenyl)-butyric acid

• CAT Number: L007332
• CAS Number: 2349961-66-4
• Molecular Formula: C25H21F2NO4
• Molecular Weight: 437.4
• Purity: ≥95%
• IUPAC Name: (3R)-4-(3,5-difluorophenyl)-3-(9H-fluoren-9-ylmethoxycarbonylamino)butanoic acid
• InChI: InChI=1S/C25H21F2NO4/c26-16-9-15(10-17(27)12-16)11-18(13-24(29)30)28-25(31)32-14-23-21-7-3-1-5-19(21)20-6-2-4-8-22(20)23/h1-10,12,18,23H,11,13-14H2,(H,28,31)(H,29,30)/t18-/m1/s1
• InChIKey: FDRZOMBFYOMDNR-GOSISDBHSA-N
• SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC(=CC(=C4)F)F)CC(=O)O

Fmoc-R-3-amino-4-(3,5-difluorophenyl)butyric acid（Cat No.:L007332）, is a specialized compound widely used in peptide synthesis and medicinal chemistry. This compound features a Fmoc (Fluorenylmethyloxycarbonyl) protective group attached to the amino group, a 3-amino group, and a 3,5-fluorophenyl substituent on the butyric acid side chain. The Fmoc protective group temporarily shields the amine, allowing precise control over chemical reactions during peptide synthesis. The 3,5-difluorophenyl moiety introduces specific chemical properties, making this compound valuable in the development of bioactive peptides and peptidomimetics used in drug discovery research and the creation of specialized materials.