Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its boronate ester group readily reacts with aryl or vinyl halides in the presence of a palladium catalyst, making it valuable in pharmaceutical, agrochemical, and materials science research. Particularly useful for introducing the benzodioxole moiety into target compounds, which is a structural motif found in bioactive molecules and natural products. Stable and easy to handle, it supports efficient and selective transformations in both small-scale discovery and larger-scale synthesis.