2-Acetylphenylboronic acid (CAS 308103-40-4)

The scientific community has been captivated by the unique properties of 2-Acetylphenylboronic acid (2-APBA), a chemical compound of great interest. This intriguing boronic acid harbors a phenyl group attached to its carbon atom, distinguishing it from its counterparts. At room temperature, it takes the form of a white solid with a melting point hovering around 145-146°C. Notably, 2-Acetylphenylboronic acid finds extensive use in organic synthesis, proving invaluable in the creation of a wide array of compounds, including agrochemicals and biopolymers. The exceptional properties of 2-Acetylphenylboronic acid have positioned it as a prominent player in scientific research. Its versatile applications encompass the synthesis of compounds ranging from pharmaceuticals to agrochemicals and biopolymers. Moreover, it has played a vital role in the creation of small molecules like peptides and nucleotides. Delving deeper into its impact, 2-Acetylphenylboronic acid has proved instrumental in the synthesis of organic compounds, spanning carbohydrates, lipids, and proteins. Operating as an electrophilic reagent, 2-Acetylphenylboronic acid exerts its mechanism of action by forming covalent bonds with electron-rich molecules. Its reactivity extends to a broad range of organic compounds, including amines, alcohols, and carboxylic acids. Typically, the reaction commences with the addition of a proton to the carbon atom of the boronic acid, culminating in the formation of a sturdy boron-oxygen bond.