H-Asp(OBzl)-NH2·HCL CAS:199118-68-8

H-Asp(OBzl)-NH2·HCl plays a crucial role in peptide synthesis, where the benzyl ester protecting group helps prevent undesired side reactions during the assembly of peptides containing aspartic acid residues, while the amino group introduces versatility in modifying peptide properties. It is extensively utilized in the preparation of modified peptides for studying protein-protein interactions, enzyme-substrate relationships, and structure-activity correlations. Researchers also employ H-Asp(OBzl)-NH2·HCl in the development of peptide-based pharmaceuticals and as a key building block for constructing novel peptides and peptidomimetics with potential therapeutic applications. Furthermore, this reagent finds application in solid-phase peptide synthesis, a fundamental method in peptide chemistry and drug discovery efforts. Its utility extends to investigations in bioconjugation and chemical biology, facilitating the conjugation of peptides to other molecules for targeted delivery or diagnostic purposes. Moreover, H-Asp(OBzl)-NH2·HCl contributes to advancing our understanding of peptide structure-function relationships and serves as a critical component in exploring diverse aspects of peptide science. Overall, it stands as an indispensable tool, enabling researchers to delve into the intricacies of peptide chemistry and its implications for biomedical research, drug development, and potential therapeutic interventions.