(S)-(+)-N-(2,3-Epoxypropyl)phthalimide CAS: 161596-47-0
Catalog Number | XD93828 |
Product Name | (S)-(+)-N-(2,3-Epoxypropyl)phthalimide |
CAS | 161596-47-0 |
Molecular Formula | C11H9NO3 |
Molecular Weight | 203.19 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
(S)-(+)-N-(2,3-Epoxypropyl)phthalimide, also known as (S)-(+)-2,3-epoxypropylphthalimide, is a specific enantiomer of a compound with potential applications in various fields, particularly in the realm of organic synthesis and chiral chemistry.One of the primary uses of (S)-(+)-N-(2,3-Epoxypropyl)phthalimide is its role as a chiral building block in organic synthesis. Chirality refers to the property of molecules to exist in mirror-image forms, known as enantiomers. As an enantiomerically pure compound, (S)-(+)-N-(2,3-Epoxypropyl)phthalimide can be used to selectively introduce chirality into other molecules during chemical reactions. This is essential in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals where chirality plays a crucial role in their biological activity.The epoxypropyl group in the compound's structure allows for the formation of new carbon-carbon or carbon-heteroatom bonds in a controlled and stereochemically precise manner. This characteristic makes (S)-(+)-N-(2,3-Epoxypropyl)phthalimide a versatile reagent for the synthesis of enantiopure epoxides, amino alcohols, or other highly functionalized derivatives. These compounds can then be employed as key intermediates or building blocks in the preparation of complex organic molecules.Additionally, the phthalimide group in the compound structure can serve as a temporary protecting group for various functional groups. Through selective deprotection, chemists can manipulate the reaction pathways and control the stereochemistry of the reactions. This allows for the synthesis of highly selective and stereospecific compounds, which is important in drug discovery and the development of novel chemical entities.Beyond organic synthesis, (S)-(+)-N-(2,3-Epoxypropyl)phthalimide may also find application in other fields. For example, it can be used as a ligand for metal catalysts, enabling asymmetric catalysis in organic reactions. It may also serve as a starting material for the synthesis of chiral auxiliaries or chiral ligands used in asymmetric synthesis, which is a valuable tool for the production of pharmaceuticals, natural products, or other biologically active compounds.In conclusion, (S)-(+)-N-(2,3-Epoxypropyl)phthalimide is a valuable compound with diverse applications in organic synthesis and chiral chemistry. Its ability to introduce chirality into molecules selectively, along with its role as a protecting group, makes it a crucial reagent for the synthesis of chiral compounds. Additionally, its potential as a ligand for asymmetric catalysis expands its utility in various chemical transformations. Further research and exploration are needed to fully uncover and utilize the compound's capabilities in different areas of science and technology.