Fmoc-(R)-3-Amino-4-(4-methoxy-phenyl)-butyric acid

• CAT Number: L007264
• CAS Number: 1421258-65-2
• Molecular Formula: C26H25NO5
• Molecular Weight: 431.5
• Purity: ≥95%
• IUPAC Name: (3R)-3-(9H-fluoren-9-ylmethoxycarbonylamino)-4-(4-methoxyphenyl)butanoic acid
• InChI: InChI=1S/C26H25NO5/c1-31-19-12-10-17(11-13-19)14-18(15-25(28)29)27-26(30)32-16-24-22-8-4-2-6-20(22)21-7-3-5-9-23(21)24/h2-13,18,24H,14-16H2,1H3,(H,27,30)(H,28,29)/t18-/m1/s1
• InChIKey: CJDCTKLQKDWTLG-GOSISDBHSA-N
• SMILES: COC1=CC=C(C=C1)CC(CC(=O)O)NC(=O)OCC2C3=CC=CC=C3C4=CC=CC=C24

Fmoc-(R)-3-Amino-4-(4-methoxyphenyl)butyric acid（Cat No.:L007264）, is a key compound in peptide chemistry. This derivative is widely used as a building block in solid-phase peptide synthesis (SPPS). Researchers utilize it in the creation of peptides for various applications, including drug development and biochemical studies. Its Fmoc (9-fluorenyl methoxycarbonyl) protection group allows for selective deprotection and subsequent peptide chain elongation, making it invaluable in the production of complex peptides. This compound’s role in peptide synthesis contributes significantly to advancements in the field of biochemistry and pharmaceutical research.