
CAS 849681-64-7
:Diphenylacetylene-4,4'-diboronic acid bis(pinacol) ester
Description:
Diphenylacetylene-4,4'-diboronic acid bis(pinacol) ester is a specialized organic compound characterized by its boronic acid ester functionality, which plays a crucial role in various chemical reactions, particularly in Suzuki coupling reactions. This compound features a diphenylacetylene backbone, contributing to its rigidity and potential for π-π stacking interactions. The presence of two boronic acid moieties allows for the formation of stable complexes with diols and other Lewis bases, enhancing its utility in organic synthesis and materials science. The pinacol ester groups provide increased stability and solubility, making the compound easier to handle in laboratory settings. Typically, this compound is used in the development of organic electronic materials, such as OLEDs and organic photovoltaics, due to its ability to form conjugated systems. Additionally, its structural characteristics may facilitate the formation of polymers or coordination complexes, expanding its applicability in various fields of research, including medicinal chemistry and catalysis. Overall, Diphenylacetylene-4,4'-diboronic acid bis(pinacol) ester is a versatile compound with significant implications in modern organic chemistry.
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Found 3 products.
4,4'-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)diphenylacetylene
CAS:Formula:C26H32B2O4Purity:%Color and Shape:SolidMolecular weight:430.15194,4,5,5-Tetramethyl-2-(4-{2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethynyl}phenyl)-1,3,2-dioxaborolane
CAS:<p>4,4,5,5-Tetramethyl-2-(4-{2-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]ethynyl}phenyl)-1,3,2-dioxaborolane</p>Purity:95%Color and Shape:SolidMolecular weight:430.15g/mol1,2-Bis(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)ethyne
CAS:Purity:95+%Molecular weight:430.1600037


