3-CHLOROPHENYLBORONIC ACID CAS :63503-60-6

3-Chlorophenylboronic acid, as a versatile chemical compound, finds wide-ranging applications in organic synthesis and materials science. It serves as a crucial building block for the creation of various pharmaceuticals, agrochemicals, and advanced materials. This compound enables the formation of carbon-carbon and carbon-heteroatom bonds, facilitating the synthesis of complex molecular structures essential in medicinal chemistry, material science, and the production of fine chemicals. The utility of 3-Chlorophenylboronic acid is particularly prominent in Suzuki-Miyaura cross-coupling reactions and other transition metal-catalyzed processes, which are pivotal in the construction of biaryl compounds. These biaryl compounds represent fundamental structural motifs with extensive applications in drug discovery, development of specialty chemicals, and the creation of functional materials. Furthermore, 3-Chlorophenylboronic acid plays a central role in the development of innovative chemical transformations, supporting advancements in synthetic methodologies and providing valuable tools for academic and industrial research. Its applications extend to the field of catalysis, where it contributes to the design of new catalytic systems and the exploration of efficient chemical processes, thus impacting diverse areas such as pharmaceutical synthesis, agrochemical production, and material science. Overall, the multifaceted uses of 3-Chlorophenylboronic acid underscore its significance as a key component in the synthesis of specialized chemicals, advanced materials, and scientific advancements in fields ranging from pharmaceuticals and agrochemicals to materials science and catalysis.