The Chemical Properties and Synthesis Applications of Boc-D-Asp(OMe)-OH
Boc-D-Asp(OMe)-OH is a specialized amino acid derivative characterized by its unique protective groups, which are integral to its utility in various synthetic applications. The tert-butyloxycarbonyl (Boc) group protects the alpha-amino function, making it stable under a range of reaction conditions but easily removable under mild acidic treatment. Concurrently, the methyl ester at the beta-carboxyl position of D-aspartic acid provides selective protection, allowing for controlled reactions primarily at the alpha-carboxyl group.
These chemical properties make Boc-D-Asp(OMe)-OH an essential component in peptide synthesis. Its incorporation into a peptide chain requires standard coupling reagents and conditions, followed by deprotection steps that selectively remove the Boc group when needed, enabling further chain elongation. This strategic protection scheme is fundamental to achieving high yields and purity in complex peptide synthesis building blocks. Many research efforts depend on obtaining this compound from reliable manufacturers to ensure consistent results.
The synthesis applications of Boc-D-Asp(OMe)-OH extend beyond simple peptide chains. It serves as a valuable chiral building block in asymmetric synthesis, contributing to the creation of enantiomerically pure compounds. Pharmaceutical chemists utilize it in the development of chiral drugs, where the specific stereochemistry of the aspartic acid residue is critical for biological activity and safety. Understanding the precise Boc-D-Asp(OMe)-OH price is often a consideration for large-scale synthesis projects.
Ningbo Inno Pharmchem Co., Ltd. is committed to supplying researchers with high-purity Boc-D-Asp(OMe)-OH, meeting the rigorous demands of advanced organic synthesis. Our manufacturing processes are designed to yield a product that excels in both chemical integrity and consistency, supporting a wide array of research endeavors. Whether for intricate peptide sequences or complex chiral molecule construction, our materials provide a reliable foundation.
By providing access to well-characterized intermediates like Boc-D-Asp(OMe)-OH, we aim to accelerate scientific discovery. Researchers who need to buy Boc-D-Asp(OMe)-OH can rely on our expertise as a manufacturer to deliver products that meet their exacting requirements for purity and performance in synthesis.
Perspectives & Insights
Agile Reader One
“The tert-butyloxycarbonyl (Boc) group protects the alpha-amino function, making it stable under a range of reaction conditions but easily removable under mild acidic treatment.”
Logic Vision Labs
“Concurrently, the methyl ester at the beta-carboxyl position of D-aspartic acid provides selective protection, allowing for controlled reactions primarily at the alpha-carboxyl group.”
Molecule Origin 88
“These chemical properties make Boc-D-Asp(OMe)-OH an essential component in peptide synthesis.”