
CAS 1246669-45-3
:9-Phenylcarbazole-2-boronic acid pinacol ester
Description:
9-Phenylcarbazole-2-boronic acid pinacol ester is an organic compound characterized by its boronic acid functionality, which is typically used in Suzuki coupling reactions, a key method in organic synthesis for forming carbon-carbon bonds. This compound features a phenylcarbazole moiety, which contributes to its potential applications in organic electronics, particularly in light-emitting diodes (LEDs) and organic photovoltaics due to its favorable electronic properties. The pinacol ester group enhances the stability and solubility of the boronic acid, making it more amenable for various chemical transformations. In terms of physical properties, compounds of this nature often exhibit moderate to high melting points and can be soluble in organic solvents. The presence of both the carbazole and boronic acid functionalities suggests potential reactivity and utility in materials science and medicinal chemistry. Overall, 9-Phenylcarbazole-2-boronic acid pinacol ester is a versatile compound with significant implications in synthetic organic chemistry and materials development.
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Found 4 products.
9-Phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)carbazole
CAS:Formula:C24H24BNO2Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:369.279H-Carbazole, 9-phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-
CAS:Formula:C24H24BNO2Purity:95%Color and Shape:SolidMolecular weight:369.26399-Phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole
CAS:<p>9-Phenyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-9H-carbazole</p>Purity:98%Molecular weight:369.26g/mol9- PHENYL-2-(4,4,5,5-TETRAMETHYL- 1,3,2-DIOXABOROLAN-2-YL)-9H-CARBAZOLE
CAS:Formula:C24H24BNO2Purity:95%Molecular weight:369.27



