Used primarily as an intermediate in organic synthesis, this compound plays a key role in the preparation of heterocyclic compounds and functionalized aromatic derivatives. Its reactivity stems from the presence of both the thiocyanate and nitro groups, enabling transformations such as cyclizations and nucleophilic substitutions. It is particularly valuable in the development of pharmaceuticals and agrochemicals where nitrogen- and sulfur-containing scaffolds are required. The electron-withdrawing nitro group enhances the electrophilicity of adjacent functional groups, facilitating reactions with amines, thiols, and other nucleophiles. Additionally, it has been explored in the synthesis of thiourea derivatives through reaction with amines, which are of interest for their biological activity.