H-Ala-OBzl·Tos CAS:42854-62-6
H-Ala-OBzl·Tos is widely employed as a key component in peptide synthesis due to its ability to protect the amine group of L-alanine. This protection allows for selective reactions with other functional groups, facilitating the precise construction of peptide sequences and enabling the study of structure-activity relationships in biologically active peptides. In the field of drug discovery and development, H-Ala-OBzl·Tos contributes to the creation of peptide-based pharmaceuticals and bioconjugates. Its role in peptide protection and subsequent deprotection processes is integral to the design and production of novel therapeutic agents. Furthermore, in biochemical research, H-Ala-OBzl·Tos enables scientists to study the functions and interactions of peptides and proteins. By providing a means to selectively protect the amine group of L-alanine, researchers can elucidate biological processes and investigate potential targets for drug development, thereby expanding the understanding of molecular mechanisms in living organisms. When working with H-Ala-OBzl·Tos, adherence to established laboratory safety protocols and handling guidelines is essential to ensure proper usage and minimize risks associated with chemical reagents. Understanding the specific reactivity and applications of H-Ala-OBzl·Tos within the context of peptide synthesis and modification is imperative for conducting successful experiments and achieving desired scientific outcomes.
Composition | C17H21NO5S |
Assay | 99% |
Appearance | white powder |
CAS No. | 42854-62-6 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |