Boc-(R,S)-3-amino-3-(2-naphthyl)propionic acid

• CAT Number: L007063
• CAS Number: 268542-15-0
• Molecular Formula: C18H21NO4
• Molecular Weight: 315.4
• Purity: ≥95%
• Storage: Store at 0-5°C
• IUPAC Name: 3-[(2-methylpropan-2-yl)oxycarbonylamino]-3-naphthalen-2-ylpropanoic acid
• InChI: InChI=1S/C18H21NO4/c1-18(2,3)23-17(22)19-15(11-16(20)21)14-9-8-12-6-4-5-7-13(12)10-14/h4-10,15H,11H2,1-3H3,(H,19,22)(H,20,21)
• InChIKey: NCQJBPXXRXOIJD-UHFFFAOYSA-N
• SMILES: CC(C)(C)OC(=O)NC(CC(=O)O)C1=CC2=CC=CC=C2C=C1

Boc-(R, S)-3-amino-3-(2-naphthyl)propionic Acid（Cat No.:L007063）, is a chiral compound used in peptide synthesis and pharmaceutical research. It consists of a protected amino acid derivative with a test-butoxy carbonyl (Boc) group on the amino group and a 2-naphthyl substituent on the alpha carbon. The chiral center in this compound allows for the creation of diverse peptide structures for drug development. The Boc protecting group temporarily shields the amino group during synthesis, preventing undesired reactions. This compound serves as a crucial building block in the production of peptides with specific biological activities, contributing to advancements in medicinal chemistry.