CAS 911708-01-5
:4-Benzylbenzeneboronic acid pinacol ester
Description:
4-Benzylbenzeneboronic acid pinacol ester is an organoboron compound characterized by the presence of a boronic acid functional group esterified with pinacol. This compound typically exhibits a white to off-white solid appearance and is soluble in organic solvents such as dichloromethane and tetrahydrofuran, while being less soluble in water. The boronic acid moiety allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and medicinal chemistry. Its structure features a benzyl group and a biphenyl system, contributing to its potential applications in the development of pharmaceuticals and agrochemicals. Additionally, the pinacol ester formation enhances the stability of the boronic acid, facilitating its handling and storage. As with many organoboron compounds, it may exhibit unique reactivity patterns, including the ability to form complexes with Lewis bases. Safety data should be consulted for handling, as organoboron compounds can have specific hazards associated with them.
Formula:C19H23BO2
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Found 4 products.
2-(4-benzylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Formula:C19H23BO2Purity:97%Color and Shape:SolidMolecular weight:294.19574-Benzylphenylboronic acid pinacol ester
CAS:<p>4-Benzylphenylboronic acid pinacol ester</p>Purity:97%Molecular weight:294.20g/mol2-(4-Benzylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Purity:97%Molecular weight:294.20001224-Benzylphenylboronic acid pinacol ester
CAS:<p>Versatile small molecule scaffold</p>Formula:C19H23BO2Purity:Min. 95%Molecular weight:294.2 g/mol



