tert-butyl 4-ethyl-2,2-dimethyl-3-oxopiperazine-1-carboxylate CAS:1936596-50-7

As a versatile building block, this molecule enables efficient medicinal chemistry and materials science. Reactions at the piperazine nitrogen systematically generate analog libraries. Additionally, reductions and additions to the carbonyl furnish targeted compounds. These transformations produce focused sets applicable for biological screening and property analysis. The tert-butyl group ensures good stability and solubility. It also serves as a monomer for tailorable polymers. Moreover, agrochemical prototypes may be developed through strategic derivatizations. Therefore, with multiple reactive sites, this synthon supports versatile synthesis of pharmaceuticals, advanced materials and agricultural chemicals via manipulations of its functional handles.