6-HYDROXY-2-NAPHTHALENEBORONICACID CAS:173194-95-1

6-Hydroxy-2-naphthaleneboronic acid serves various purposes across different fields: Medicinal Chemistry: It is extensively utilized in medicinal chemistry for the synthesis of boron-containing compounds with potential pharmaceutical applications, including anticancer agents, protease inhibitors, and enzyme inhibitors. Organic Synthesis: This compound acts as a valuable building block in organic synthesis, particularly in the preparation of complex molecules and biologically active compounds. Chemical Biology: It finds application as a tool in chemical biology research, facilitating the study of biomolecular interactions and cellular processes due to its ability to bind to biological targets such as proteins and nucleic acids. Catalysis: 6-Hydroxy-2-naphthaleneboronic acid is employed as a catalyst or ligand in various catalytic transformations, including cross-coupling reactions, Suzuki-Miyaura coupling, and C-H activation reactions. Fluorescent Probes: It is used in the development of fluorescent probes for imaging biological systems and studying cellular processes, owing to its fluorescent properties and biocompatibility. Analytical Chemistry: This compound serves as a reference material and a standard in analytical methods such as chromatography and spectroscopy for the detection and quantification of boron-containing compounds. Materials Science: Its boronic acid functionality makes it useful in the design and synthesis of functional materials for applications in sensors, electronics, and optoelectronics. In summary, 6-Hydroxy-2-naphthaleneboronic acid's versatility and reactivity make it a valuable tool in medicinal chemistry, organic synthesis, chemical biology, catalysis, and materials science, contributing to advancements in various scientific and industrial fields.