Products

(S)-(+)-2-Amino-2-phenylethanol is the enantiomer of (R)-(-)-2-Phenylglycinol, with the same molecular formula but a different spatial arrangement. Here are some of the effects and benefits associated with (S)-(+)-2-Amino-2-phenylethanol:Asymmetric Synthesis: (S)-(+)-2-Amino-2-phenylethanol is commonly used as a chiral auxiliary or resolving agent in asymmetric synthesis. It can be employed to selectively convert prochiral compounds into enantiomerically pure products. By utilizing this compound, chemists can access single enantiomers, which are crucial in the production of pharmaceuticals and fine chemicals.Ligand in Coordination Chemistry: (S)-(+)-2-Amino-2-phenylethanol can serve as a ligand in coordination chemistry and catalytic reactions. It can coordinate to metal centers and influence the stereochemistry of the resulting complexes. This compound's presence can enhance the selectivity and efficiency of metal-catalyzed reactions, such as asymmetric hydrogenation or asymmetric epoxidation.Chiral Solvent: Due to its chiral nature, (S)-(+)-2-Amino-2-phenylethanol is often used as a chiral solvent in various organic reactions. It can provide a chiral environment, affecting the reaction outcome and allowing for enantioselective transformations.Pharmaceutical Applications: (S)-(+)-2-Amino-2-phenylethanol is used in the synthesis of pharmaceuticals and biologically active compounds. Its chiral framework is beneficial for the development of enantiopure drugs. This compound can be utilized as a building block or intermediate in the synthesis of chiral pharmaceutical molecules.Resolving Agent: (S)-(+)-2-Amino-2-phenylethanol can be employed as a resolving agent to separate racemic mixtures into their individual enantiomers. Through the formation of diastereomeric salts or complexes, it can facilitate the isolation and purification of enantiopure compounds.Biological Activity: (S)-(+)-2-Amino-2-phenylethanol has exhibited biological activities, including antihypertensive and antiviral effects. It has been studied for its potential therapeutic application in the treatment of hypertension and viral infections.Like any chemical compound, (S)-(+)-2-Amino-2-phenylethanol should be handled with care, following appropriate safety protocols and regulations. As with its (R)-enantiomer, it is advisable to consult with experts or professionals in the field before utilizing it in research or pharmaceutical development.