CAS 264144-59-4
:cis-Stilbeneboronic acid pinacol cyclic ester
Description:
Cis-Stilbeneboronic acid pinacol cyclic ester, identified by its CAS number 264144-59-4, is a boronic acid derivative characterized by its unique structural features. This compound typically exhibits a pinacol cyclic ester formation, which contributes to its stability and reactivity. The presence of the boronic acid functional group allows for participation in various chemical reactions, particularly in Suzuki coupling reactions, making it valuable in organic synthesis and materials science. The cis configuration of the stilbene moiety imparts specific stereochemical properties, influencing its interactions and reactivity. Additionally, this compound may exhibit solubility in organic solvents, which is common for boronic acids and their derivatives. Its applications can extend to medicinal chemistry, where boronic acids are often explored for their potential in drug development and as molecular probes. Overall, cis-Stilbeneboronic acid pinacol cyclic ester is a versatile compound with significant implications in synthetic organic chemistry and related fields.
Formula:C20H23BO2
InChI:InChI=1/C20H23BO2/c1-19(2)20(3,4)23-21(22-19)18(17-13-9-6-10-14-17)15-16-11-7-5-8-12-16/h5-15H,1-4H3/b18-15+
Synonyms:- cis-(1,2-Diphenylethenyl)boronic acid pinacol cyclic ester
- 2-[(Z)-1,2-diphenylvinyl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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Found 2 products.
1,3,2-Dioxaborolane, 2-[(1Z)-1,2-diphenylethenyl]-4,4,5,5-tetramethyl-
CAS:Formula:C20H23BO2Purity:95%Color and Shape:SolidMolecular weight:306.2064(Z)-2-(1,2-Diphenylvinyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS:Purity:95% mix TBC as stabilizerMolecular weight:306.2099915

