4-(N-Boc-amino)-1,6-heptanedioic acid is primarily used in organic synthesis as a building block for the preparation of more complex molecules. It is particularly valuable in peptide chemistry, where the Boc (tert-butyloxycarbonyl) group serves as a protective group for amines during the synthesis process. This compound allows for the controlled introduction of amino functionalities into target molecules, ensuring that reactions proceed with high specificity and yield. Additionally, it is employed in the development of pharmaceutical intermediates, where its dual carboxylic acid groups enable the formation of amide bonds, essential for constructing bioactive compounds. Its stability and reactivity make it a versatile reagent in medicinal chemistry and drug discovery.