Fmoc-L-3-Trifluoromethylphenylalanine

• CAT Number: L006869
• CAS Number: 205526-27-8
• Molecular Formula: C25H20F3NO4
• Molecular Weight: 455.4
• Purity: ≥95%
• Storage: 2-8°C
• IUPAC Name: (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-[3-(trifluoromethyl)phenyl]propanoic acid
• InChI: InChI=1S/C25H20F3NO4/c26-25(27,28)16-7-5-6-15(12-16)13-22(23(30)31)29-24(32)33-14-21-19-10-3-1-8-17(19)18-9-2-4-11-20(18)21/h1-12,21-22H,13-14H2,(H,29,32)(H,30,31)/t22-/m0/s1
• InChIKey: AJMRBDCOLBEYRZ-QFIPXVFZSA-N
• SMILES: C1=CC=C2C(=C1)C(C3=CC=CC=C32)COC(=O)NC(CC4=CC(=CC=C4)C(F)(F)F)C(=O)O

Fmoc-L-3-trifluoromethylphenylalanine（Cat No.:L006869）, is an important amino acid derivative used in peptide chemistry and solid-phase peptide synthesis. Its molecular structure incorporates a trifluoromethyl phenylalanine moiety protected with a fluorenylmethyloxycarbonyl (Fmoc) group. Researchers utilize this compound to incorporate the trifluoromethyl phenylalanine residue into peptides, enabling the study of structure-activity relationships in biological systems. The Fmoc protecting group ensures selective reactions during peptide synthesis. This compound finds applications in the development of peptide-based drugs and bioactive molecules.