This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic ester intermediate. Its structure, featuring a pyrazole ring with the nitrogen protected by a trimethylsilyl ethoxymethyl (SEM) group, makes it valuable for constructing complex molecules in pharmaceutical and agrochemical research. The SEM protecting group enhances its stability during reactions, allowing for selective deprotection when needed. This compound is often employed in the development of biologically active compounds, including potential drug candidates, due to its ability to facilitate the formation of carbon-carbon bonds in a controlled manner.