This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of biaryl or styryl structures. The 1H-pyrrol-1-yl substituent at the 2-position provides electronic modulation to the pyridine ring, potentially enhancing solubility, reactivity, or biological interactions in the resulting compounds. Additionally, its fluorine substituent can enhance the biological activity and metabolic stability of the resulting compounds, making it useful in drug discovery and medicinal chemistry research.