Boc-L-Glutamic acid 5-benzylester

• CAT Number: M066429
• CAS Number: 13574-13-5
• Molecular Formula: C17H23NO6
• Molecular Weight: 337.37
• Purity: ≥95%
• Storage: 2-8°C
• IUPAC Name: (2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-oxo-5-phenylmethoxypentanoic acid
• InChI: InChI=1S/C17H23NO6/c1-17(2,3)24-16(22)18-13(15(20)21)9-10-14(19)23-11-12-7-5-4-6-8-12/h4-8,13H,9-11H2,1-3H3,(H,18,22)(H,20,21)/t13-/m0/s1
• InChIKey: AJDUMMXHVCMISJ-ZDUSSCGKSA-N
• SMILES: CC(C)(C)OC(=O)NC(CCC(=O)OCC1=CC=CC=C1)C(=O)O

Boc-L-Glutamic acid 5-benzyl ester （Cat No.:M066429）, is a compound used in peptide synthesis and organic chemistry. It is derived from L-glutamic acid, an amino acid, by substituting the carboxylic acid group with a Boc (tert-butyloxycarbonyl) protecting group and attaching a benzyl ester at the fifth position. This derivative aids in peptide assembly, offering protection for specific functional groups during synthesis. After the desired sequence is built, these protecting groups can be selectively removed to reveal the unmodified amino acids. This process contributes to the creation of complex peptides and the study of protein structures.