(R)-3-((tert-Butoxycarbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic Acid

• CAT Number: R023668
• CAS Number: 486460-00-8
• Molecular Formula: C15H18F3NO4
• Molecular Weight: 333.31
• Purity: ≥95%
• Synonyms: (βR)-β-[[(1,1-Dimethylethoxy)carbonyl]amino]-2,4,5-trifluoro-benzenebutanoic Acid; 3R)-3-[(1,1-Dimethylethoxycarbonyl)amino]-4-(2,4,5-trifluorophenyl)butanoic Acid; (3R)-3-[(tert-Butoxycarbonyl)amino]-4-(2,4,5-trifluorophenyl)butanoic Acid
• Storage: -20°C
• IUPAC Name: (3R)-3-[(2-methylpropan-2-yl)oxycarbonylamino]-4-(2,4,5-trifluorophenyl)butanoic acid
• InChI: InChI=1S/C15H18F3NO4/c1-15(2,3)23-14(22)19-9(6-13(20)21)4-8-5-11(17)12(18)7-10(8)16/h5,7,9H,4,6H2,1-3H3,(H,19,22)(H,20,21)/t9-/m1/s1
• InChIKey: TUAXCHGULMWHIO-SECBINFHSA-N
• SMILES: CC(C)(C)OC(=O)NC(CC1=CC(=C(C=C1F)F)F)CC(=O)O

(R)-3-((tert-Butoxycarbonyl)amino)-4-(2,4,5-trifluorophenyl)butanoic acid (Cat No.: R023668) is a chiral, Boc-protected amino acid analog featuring a trifluorinated aromatic side chain. This compound is useful in medicinal chemistry and peptide design, where fluorinated residues can enhance metabolic stability, bioavailability, and binding affinity. The tert-butoxycarbonyl (Boc) group allows for acid-labile protection during synthesis, facilitating incorporation into complex peptide sequences. Its (R)-configuration supports stereoselective synthesis of biologically active compounds, including peptidomimetics, enzyme inhibitors, and fluorinated drug candidates in pharmaceutical research.