CAS: 870004-04-9

(4-Vinylphenyl)boronic acid pinacol ester

Stability Hygroscopic Applications 2-(4-ethenylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

(4-Vinylphenyl)boronic acid pinacol ester is a compound that has been synthesized for use in organic synthesis. It is an unsymmetrical molecule with vinyl groups and chloride substituents. The vinyl groups are substituted at positions 1 and 4 on the boron atom, while the chloride substituents are on the phenyl group at position 2 and on the acetylene group at position 3. (4-Vinylphenyl)boronic acid pinacol ester can be used as a nucleophile to form new molecules by reacting with an electrophile. This strategy has been demonstrated by attaching it to trimethylsilylacetylene, which is then reacted with benzene derivatives. (4-Vinylphenyl)boronic acid pinacol ester can also be combined with other stilbene derivatives to form biphenyl compounds.