(αS,3S)-α-[(tert-Butyloxycarbonyl)aMino]-2-oxo-3-pyrrolidinepropanoic acid Methyl Ester CAS: 328086-60-8
Catalog Number | XD93394 |
Product Name | (αS,3S)-α-[(tert-Butyloxycarbonyl)aMino]-2-oxo-3-pyrrolidinepropanoic acid Methyl Ester |
CAS | 328086-60-8 |
Molecular Formula | C13H22N2O5 |
Molecular Weight | 286.33 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
(αS,3S)-α-[(tert-Butyloxycarbonyl)amino]-2-oxo-3-pyrrolidinepropanoic acid methyl ester, also known as Boc-Amino acid methyl ester, is an important compound in the field of organic synthesis and peptide chemistry.Boc-Amino acid methyl ester serves as a protected form of amino acids, where the Boc (tert-butyloxycarbonyl) group is used to protect the amino group during reactions. This compound is primarily utilized in peptide synthesis to introduce specific amino acids into peptide chains.Peptides are short chains of amino acids that play critical roles in biological systems. They are involved in various processes such as signaling, enzyme regulation, and structural support. Peptide synthesis involves the stepwise assembly of amino acids to create specific sequences that mimic natural peptides or create novel structures with desired properties.Boc-Amino acid methyl ester is commonly used as a building block in solid-phase peptide synthesis (SPPS), which is one of the most widely employed methods to construct peptides. In SPPS, the peptide chain is synthesized in a stepwise manner on a solid support, typically using an amino acid derivative with a temporary protecting group. Boc-Amino acid methyl ester is an ideal starting material for SPPS because of its stability, solubility, and compatibility with other peptide synthesis reagents.During peptide synthesis, Boc-Amino acid methyl ester is added to the growing peptide chain through amide bond formation. The Boc protecting group prevents unwanted side reactions and ensures selective coupling of the amino acid to the peptide chain. Once the desired sequence is achieved, the Boc group is removed under mild conditions, revealing the free amino group for further modifications or peptide characterization.In addition to peptide synthesis, Boc-Amino acid methyl ester can also be used in the preparation of various pharmaceutical intermediates, agrochemicals, and other organic compounds. Its easy handling, stability, and compatibility with standard reaction conditions make it a versatile building block for organic synthesis.Overall, Boc-Amino acid methyl ester is a valuable tool in peptide synthesis and organic chemistry. Its role as a protected form of amino acids allows for the efficient assembly of peptide chains and the creation of diverse peptide structures for research, drug discovery, and therapeutic applications.