N-Boc-glycine isopropylester is widely used in organic synthesis, particularly in peptide chemistry. It serves as a protected form of glycine, where the Boc (tert-butoxycarbonyl) group safeguards the amino functionality during reactions. This compound is often employed in the stepwise construction of peptides, allowing for selective deprotection and coupling with other amino acids or intermediates. Additionally, it is utilized in the preparation of modified peptides or peptidomimetics for pharmaceutical research. Its isopropyl ester group enhances solubility in organic solvents, making it suitable for various synthetic procedures. This chemical is also valuable in the development of bioactive molecules and drug candidates, where controlled amino acid incorporation is essential.