D-Phenylalanine, N-[N-[(1,1-dimethylethoxy)carbonyl]-D-leucyl]-, phenylmethyl ester

• CAT Number: I043085
• CAS Number: 159549-97-0
• Molecular Formula: C27H36N2O5
• Molecular Weight: 468.59
• Purity: ≥95%
• Synonyms: benzyl (2R)-2-[[(2R)-4-methyl-2-[(2-methylpropan-2-yl)oxycarbonylamino]pentanoyl]amino]-3-phenylpropanoate
• InChI: InChI=1S/C27H36N2O5/c1-19(2)16-22(29-26(32)34-27(3,4)5)24(30)28-23(17-20-12-8-6-9-13-20)25(31)33-18-21-14-10-7-11-15-21/h6-15,19,22-23H,16-18H2,1-5H3,(H,28,30)(H,29,32)/t22-,23-/m1/s1
• InChIKey: IKZFNIAMQFYRSM-DHIUTWEWSA-N
• SMILES: CC(C)C[C@H](C(=O)N[C@H](CC1=CC=CC=C1)C(=O)OCC2=CC=CC=C2)NC(=O)OC(C)(C)C

D-Phenylalanine, N-[N-[(1,1-dimethylethoxy)carbonyl]-D-leucyl]-, phenylmethyl ester（Cat No.:I043085）is a peptide derivative consisting of D-phenylalanine and D-leucine, with a protective carbamate group (1,1-dimethylethoxy) to prevent unwanted reactions during synthesis. The phenylmethyl ester group is added to enhance solubility and stability in certain chemical environments. This compound is commonly used in peptide synthesis and drug development research, where it can serve as a building block or intermediate in the creation of bioactive peptides. The structure allows for studies in proteomics, enzymology, and for exploring novel therapeutic peptide formulations.