9-Phenyl-9H-carbazol-3-ylboronic acid CAS: 854952-58-2
Catalog Number | XD93523 |
Product Name | 9-Phenyl-9H-carbazol-3-ylboronic acid |
CAS | 854952-58-2 |
Molecular Formula | C18H14BNO2 |
Molecular Weight | 287.12 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
9-Phenyl-9H-carbazol-3-ylboronic acid is a chemical compound that plays a crucial role in several areas of organic chemistry, medicinal chemistry, and materials science.One significant use of 9-Phenyl-9H-carbazol-3-ylboronic acid is in the synthesis of various pharmaceuticals. The boronic acid functionality on the carbazole ring enables it to participate in important cross-coupling reactions, such as Suzuki-Miyaura coupling. This reaction is widely used in the pharmaceutical industry to create carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. By incorporating 9-Phenyl-9H-carbazol-3-ylboronic acid into the reaction, the resulting products can possess enhanced biological activity. This compound acts as a valuable intermediate for the preparation of biologically active molecules, including anticancer agents, antiviral drugs, and other therapeutic agents.Moreover, 9-Phenyl-9H-carbazol-3-ylboronic acid also finds applications in materials science. Its boronic acid group can participate in cross-linking reactions, allowing for the synthesis of polymers and dendrimers. These materials exhibit unique properties such as high thermal stability, good mechanical strength, and interesting optical properties, making them suitable for use in various industrial applications. The carbazole moiety in 9-Phenyl-9H-carbazol-3-ylboronic acid also provides the potential for electroluminescent properties, making it useful in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices.Additionally, this compound can be used as a building block for the synthesis of functional materials, such as liquid crystals and conjugated polymers. These materials have applications in the field of display technology, organic electronics, and photovoltaics. The functional groups present in 9-Phenyl-9H-carbazol-3-ylboronic acid allow for the modification and tailoring of the resulting materials to achieve desired properties, such as high charge carrier mobility or efficient energy transfer.In conclusion, 9-Phenyl-9H-carbazol-3-ylboronic acid is a versatile compound with significant applications in pharmaceuticals and materials science. Its boronic acid functionality enables the construction of biologically active molecules, expanding the range of therapeutic options. Furthermore, its use in the synthesis of polymers, dendrimers, and functional materials allows for the development of innovative products in the fields of organic electronics, optoelectronics, and energy-related technologies. The unique properties of 9-Phenyl-9H-carbazol-3-ylboronic acid make it a valuable tool for researchers and chemists working in various scientific disciplines.