(2S,4S)-1-Boc-4-Aminopyrrolidine-2-carboxylic acid CAS:132622-66-3
(2S,4S)-1-Boc-4-aminopyrrolidine-2-carboxylic acid serves as a vital intermediate in the synthesis of complex, bioactive compounds with potential pharmaceutical applications. Its chiral nature and unique structural features position it as a key component for the creation of enantiopure compounds, which are essential in drug development. By incorporating this building block into molecular frameworks, researchers can explore new drug candidates targeting therapeutic areas such as antivirals, antineoplastics, or central nervous system disorders. In medicinal chemistry, this compound may serve as a starting point for designing potential drug candidates, leveraging its stereochemistry to modulate biological activity and pharmacokinetic properties. The Boc protection of the amino group provides control over reactivity and selectivity during subsequent synthetic transformations, enabling the construction of diverse chemical structures. Furthermore, in academic and industrial settings, researchers can utilize this building block to prepare libraries of diverse derivatives for structure-activity relationship studies, facilitating the identification of lead compounds with desired biological effects. Its role in chemical synthesis extends to the production of pharmaceutical intermediates and the development of novel synthetic methodologies, showcasing its broad utility across scientific disciplines. Overall, (2S,4S)-1-Boc-4-aminopyrrolidine-2-carboxylic acid plays a crucial role in the pursuit of innovative drug discovery and asymmetric synthesis, providing a platform for the development of diverse biologically active molecules and pharmaceutical intermediates.
Composition | C10H18N2O4 |
Assay | 99% |
Appearance | White power |
CAS No. | 132622-66-3 |
Packing | Small and bulk |
Shelf Life | 2 years |
Storage | Store in cool and dry area |
Certification | ISO. |