(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-hydroxy-3-iodophenyl)propanoic acid, commonly referred to as $name$, is a valuable compound in chemical synthesis due to its versatile applications. This compound serves as a key building block in the creation of peptide-based structures, particularly in the field of peptide synthesis. When used in chemical reactions, $name$ acts as a protected amino acid derivative, providing a stable platform for the selective modification of peptides. Its tert-butoxycarbonyl (Boc) protecting group shields the amino group, allowing for controlled peptide bond formation without interference. The hydroxyl and iodine functionalities in the molecule also offer opportunities for further derivatization and diversification of the peptide chain.In peptide synthesis, the strategic incorporation of (S)-2-((tert-Butoxycarbonyl)amino)-3-(4-hydroxy-3-iodophenyl)propanoic acid enables the construction of structurally complex and biologically relevant peptides. By carefully manipulating the reactive sites of the compound, chemists can tailor the properties of the peptides for various applications, such as drug development, biochemical studies, and materials science.Overall, (S)-2-((tert-Butoxycarbonyl)amino)-3-(4-hydroxy-3-iodophenyl)propanoic acid plays a crucial role in the synthesis of intricate peptide structures, offering chemists a powerful tool for designing and engineering novel molecules with specific functions and properties.
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