Application

Phenylboronic acid may be employed in the following reactions:Rhodium-catalyzed intramolecular amination. Pd-catalyzed direct arylation. Mizoroki-Heck and Suzuki-Miyaura coupling reactions catalyzed by palladium nanoparticles. Palladium-catalyzed stereoselective Heck-type reaction. Highly effective Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water. Phenylboronic acid may be employed as reagent in the preparation of:Ni(II) pincer complex and Pd(II) pyridoxal hydrazone metallacycles as catalysts for the Suzuki-Miyaura cross-coupling reactions.N-type polymers for all-polymer solar cells. Novel series of potent and selective mTOR kinase inhibitors. Inhibitors of lactate dehydrogenase against cancer cell proliferation.

General description

Phenylboronic acid (PBA) is an organoboronic acid. It behaves as a molecular receptor that can attach to compounds containing cis-diol group. Microwave-assisted Suzuki coupling of aryl chlorides with phenylboronic acid in the presence of Pd/C (catalyst) and water (solvent) has been described. Palladium-catalyzed cross-coupling reaction of phenylboronicacid with haloarenes to afford biaryls has been reported.

Other Notes

Contains varying amounts of phenylboronic anhydride

Packaging

1 g in glass bottle

10 g in poly bottle

50 g in glass bottle