2-(2-Ethenylphenyl)-1,3,2-dioxaborinane, identified by its CAS number 850567-61-2, is an organoboron compound characterized by the presence of a dioxaborinane ring and a vinyl-substituted phenyl group. This compound typically exhibits a boron atom coordinated to two oxygen atoms within a cyclic structure, contributing to its unique reactivity and stability. The vinyl group enhances its potential for polymerization and cross-linking reactions, making it of interest in materials science and organic synthesis. The presence of the boron atom also suggests potential applications in catalysis and as a reagent in various chemical transformations, particularly in Suzuki coupling reactions. Additionally, the compound may exhibit interesting optical properties due to the conjugated system formed by the vinyl and phenyl groups. Overall, 2-(2-Ethenylphenyl)-1,3,2-dioxaborinane represents a versatile building block in organic chemistry, with implications for both academic research and industrial applications.

2-(2-Ethenylphenyl)-1,3,2-dioxaborinane

850567-61-2: 2-(2-Ethenylphenyl)-1,3,2-dioxaborinane, 2-(2-Vinylphenyl)-1,3,2-dioxaborinane, 1,3,2-Dioxaborinane, 2-(2-ethenylphenyl)-

2-(2-Vinylphenyl)-1,3,2-dioxaborinane

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CAS 850567-61-2: 2-(2-Ethenylphenyl)-1,3,2-dioxaborinane

2-(2-Vinylphenyl)-1,3,2-dioxaborinane

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(2-Vinylphenylboronic acid, propanediol cyclic ester

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