H-D-Ala-OBzl ·Tos CAS:41036-32-2
H-D-Ala-OBzl·Tos plays a critical role in peptide synthesis and modification due to its ability to selectively protect the amine group of D-alanine. This protection enables precise manipulation of peptide sequences by allowing selective reactions with other functional groups, facilitating the construction of complex peptide structures essential for studying structure-activity relationships in biologically active peptides. In drug discovery and development, H-D-Ala-OBzl·Tos contributes to the creation of peptide-based pharmaceuticals and bioconjugates. Its role in protecting the amine group of D-alanine and subsequent deprotection processes is integral to the design and production of novel therapeutic agents with potential applications in targeted drug delivery and precision medicine. Furthermore, in biochemical research, H-D-Ala-OBzl·Tos provides scientists with a tool to study the functions and interactions of peptides and proteins. By enabling selective protection of the amine group of D-alanine, researchers can investigate biological processes and explore potential targets for drug development, thereby contributing to the broader understanding of molecular mechanisms in living organisms. When working with H-D-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-D-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. | 41036-32-2 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |