(3S,4S)-4-((tert-Butoxycarbonyl)amino)-3-hydroxy-6-methylheptanoic acid

The compound (3S,4S)-4-((tert-Butoxycarbonyl)amino)-3-hydroxy-6-methylheptanoic acid, also known by the name $name$, plays a crucial role in chemical synthesis processes. This compound is commonly utilized as a chiral building block due to its unique stereochemistry and functional groups. In chemical synthesis, (3S,4S)-4-((tert-Butoxycarbonyl)amino)-3-hydroxy-6-methylheptanoic acid serves as a key precursor in the production of various pharmaceuticals, agrochemicals, and specialty chemicals.The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective manipulation of the amino group, enabling controlled reactions and facilitating the synthesis of complex molecules. The hydroxy and methyl substituents further contribute to the versatility of this compound in creating diverse chemical structures. By incorporating (3S,4S)-4-((tert-Butoxycarbonyl)amino)-3-hydroxy-6-methylheptanoic acid into synthetic pathways, chemists can access enantiomerically pure compounds essential for drug discovery, material science, and other fields requiring precise molecular design.