Phenylboronic acid (contains varying amounts of Anhydride) (C09-1016-081)

Contains varying amounts of phenylboronic anhydride.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.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. Specifications and Purity: 99.5%. MDL Number: MFCD00002103. Molecular Formula: C6H7BO2. Molecular Weight: 121.93. EC Number: 202-701-9. PubChem CID: 66827. Isomeric SMILES: B(C1=CC=CC=C1)(O)O. Beilstein Registry Number: 970972. Related Document: https://ald-pub-files.oss-cn-shanghai.aliyuncs.com/aladdinsci/pdp/sds/1/P396095-SCI_5f41cc330c5baefd5c3afafe31800723.pdf.