(3,5-Diphenylphenyl)boronicacid CAS:128388-54-5
Catalog Number | XD96072 |
Product Name | (3,5-Diphenylphenyl)boronicacid |
CAS | 128388-54-5 |
Molecular Formula | C18H15BO2 |
Molecular Weight | 274.12 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
(3,5-Diphenylphenyl)boronic acid, also known as diphenylphenylboronic acid, is a compound that has been studied for its potential effects in various fields. Here are some of its known or potential effects:One notable application of (3,5-Diphenylphenyl)boronic acid is in organic synthesis. As a boronic acid, it can form stable complexes with various functional groups, making it a valuable building block in the synthesis of complex organic molecules. This compound can undergo reactions such as Suzuki-Miyaura cross-coupling reactions to create new carbon-carbon or carbon-heteroatom bonds. Its unique structure, with two phenyl groups and a boronic acid moiety, contributes to its reactivity and can be harnessed to create diverse organic compounds.Furthermore, (3,5-Diphenylphenyl)boronic acid has shown potential in medicinal chemistry. Boronic acids can inhibit specific protein targets by forming reversible complexes with their active sites. This property makes them useful in developing therapeutics targeting diseases such as cancer. By targeting specific proteins involved in disease pathways, this compound can potentially disrupt their function and contribute to the development of novel drugs.In addition to its application in organic synthesis and medicinal chemistry, (3,5-Diphenylphenyl)boronic acid has demonstrated potential in materials science. Boronic acids have been employed as building blocks for the synthesis of organic semiconductors used in electronic devices. The unique structure of this compound, with its phenyl groups and boronic acid functionality, can contribute to the electronic properties of these materials, such as charge transport and light emission. This makes it useful in the development of organic field-effect transistors (OFETs), organic light-emitting diodes (OLEDs), and organic photovoltaics (OPVs).Additionally, (3,5-Diphenylphenyl)boronic acid has been explored for its potential in chemical sensing applications. The boronic acid group can selectively bind to certain analytes, such as saccharides, forming reversible complexes. This property has been utilized in the development of sensors for detecting specific analytes, particularly glucose in biological samples. By incorporating this compound into suitable platforms, such as polymers or nanomaterials, highly sensitive and selective detection of target analytes can be achieved.In summary, (3,5-Diphenylphenyl)boronic acid exhibits various effects and potential applications in organic synthesis, medicinal chemistry, materials science, and chemical sensing. Its ability to form stable complexes with various functional groups, along with its unique structural features, makes it a valuable compound in these fields. Continued research and exploration of this compound could uncover further applications and optimize its potential effects.