
CAS 884336-44-1
:9,9-Spirodifluorene-2-Boronic acid pinacol ester
Description:
9,9-Spirodifluorene-2-boronic acid pinacol ester is an organoboron compound characterized by its unique spiro structure, which consists of a boronic acid moiety attached to a spiro-difluorene framework. This compound typically exhibits properties associated with both boron and aromatic systems, including potential applications in organic electronics, such as in the development of organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). The presence of the boronic acid functionality allows for versatile reactivity, particularly in Suzuki coupling reactions, making it valuable in synthetic organic chemistry. Additionally, the pinacol ester group enhances its stability and solubility in organic solvents. The compound's molecular structure contributes to its electronic properties, which can be tuned for specific applications in materials science. Overall, 9,9-Spirodifluorene-2-boronic acid pinacol ester is notable for its potential in advanced materials and its role in facilitating various chemical transformations.
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Found 4 products.
2-(9,9'-Spirobi[fluoren]-7-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C31H27BO2Purity:>98.0%(T)(HPLC)Color and Shape:White to Almost white powder to crystalMolecular weight:442.379,9-Spirodifluorene-2-Boronic acid pinacol ester
CAS:Formula:C31H27BO2Purity:97%Color and Shape:SolidMolecular weight:442.35592-(9,9’-Spirobi[Fluoren]-7-yl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane
CAS:<p>2-(9,9’-Spirobi[Fluoren]-7-yl)-4,4,5,5-Tetramethyl-1,3,2-Dioxaborolane</p>Purity:98%Molecular weight:442.36g/mol2-(9,9′-Spirobi[fluoren]-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Purity:97%Molecular weight:442.3699951



