AW12776
Packsize | Purity | Availability | Price | Discounted Price | Quantity | |
---|---|---|---|---|---|---|
50mg | 95% | 1 week | $530.00 | $371.00 | - + | |
100mg | 95% | 1 week | $766.00 | $537.00 | - + |
*All products are for research use only and not intended for human or animal use.
*All prices are in USD.
Catalog Number: | AW12776 |
Chemical Name: | Phenylmethanesulfinamide |
CAS Number: | 112599-81-2 |
Molecular Formula: | C7H9NOS |
Molecular Weight: | 155.2175 |
MDL Number: | MFCD28118620 |
SMILES: | NS(=O)Cc1ccccc1 |
Phenylmethanesulfinamide, also known as sulfinylamine or PhSO2NH2, serves as a versatile reagent in chemical synthesis due to its unique properties and reactivity. This compound is widely used in various organic reactions to introduce chiral sulfur-containing functionalities into organic molecules. In asymmetric synthesis, Phenylmethanesulfinamide can act as a chiral auxiliary, allowing for the enantioselective transformation of substrates. By forming diastereomeric complexes, this reagent can steer the stereochemical outcome of reactions, enabling the synthesis of enantiomerically enriched compounds. Additionally, Phenylmethanesulfinamide is employed in the desymmetrization of prochiral substrates, leading to the formation of chiral products with high optical purity. Its ability to transfer chirality under mild conditions makes it a valuable tool for the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Furthermore, Phenylmethanesulfinamide can participate in a range of transformations such as asymmetric hydroamination, asymmetric allylation, and asymmetric reduction reactions. Its unique sulfonamide moiety confers stability and enables selective transformations, contributing to its utility in complex molecule synthesis.