Boc-Phe-Gly-OH

• CAT Number: I043239
• CAS Number: 25616-33-5
• Molecular Formula: C16H22N2O5
• Molecular Weight: 322.36
• Purity: ≥95%
• Synonyms: 2-[[(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-phenylpropanoyl]amino]acetic acid
• InChI: InChI=1S/C16H22N2O5/c1-16(2,3)23-15(22)18-12(14(21)17-10-13(19)20)9-11-7-5-4-6-8-11/h4-8,12H,9-10H2,1-3H3,(H,17,21)(H,18,22)(H,19,20)/t12-/m0/s1
• InChIKey: MJRWXIQFTMLYFG-LBPRGKRZSA-N
• SMILES: CC(C)(C)OC(=O)N[C@@H](CC1=CC=CC=C1)C(=O)NCC(=O)O

Boc-Phe-Gly-OH（Cat No.:I043239）is a dipeptide derivative in which the phenylalanine (Phe) residue is protected at the N-terminal by a tert-butoxycarbonyl (Boc) group, while the glycine (Gly) residue remains free at the C-terminal. The Boc group prevents side reactions during peptide synthesis, particularly in solid-phase peptide synthesis (SPPS), allowing for controlled deprotection when needed. This compound is used in the synthesis of peptides, especially for introducing phenylalanine and glycine into sequences where aromatic and small amino acids are required. It is valuable in pharmaceutical, biochemical, and research applications.