4-Chlorophenylboronic acid CAS:1679-18-1

4-Chlorophenylboronic acid, often denoted as CPBA, plays a crucial role in the synthesis of biaryl compounds through Suzuki-Miyaura cross-coupling reactions. This synthetic method allows for the efficient construction of complex molecular architectures, making CPBA a key building block in organic chemistry. In medicinal chemistry, derivatives of 4-chlorophenylboronic acid have exhibited promising pharmacological activities. Researchers have explored their potential as inhibitors of various enzymes and receptors implicated in disease pathways, including kinases and proteases. The ability of CPBA derivatives to modulate biological processes makes them attractive candidates for drug discovery efforts. Furthermore, 4-chlorophenylboronic acid derivatives have found applications in materials science, particularly in the development of functional polymers and molecular recognition systems. By incorporating CPBA moieties into polymer matrices, researchers have created materials with stimuli-responsive behavior, enabling applications in drug delivery, sensing, and molecular separations. The versatility of 4-chlorophenylboronic acid extends to supramolecular chemistry, where it participates in the assembly of complex structures through non-covalent interactions. These supramolecular assemblies exhibit tunable properties, making them suitable for diverse applications, from catalysis to molecular sensing. In summary, 4-chlorophenylboronic acid represents a versatile building block with wide-ranging applications in organic synthesis, medicinal chemistry, and materials science. Its unique chemical properties make it a valuable tool for the design and development of functional molecules and materials with applications in pharmaceuticals, diagnostics, and beyond. Continued research into the synthetic methodologies and applications of CPBA derivatives is expected to yield further insights into their potential in various scientific and technological fields.