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Structure of 138-15-8
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Phenylboronic acid is a highly stable receptor ligand used in cross-coupling reactions and drug delivery.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.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.
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GHS Pictogram :
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GHS No : GHS05
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Signal Word : Danger
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UN#: 1759
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Class : 8
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Packing Group : Ⅲ
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Hazard Statements : H314
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Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
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Lot numbers can be found on the outside label of a product: