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2-Biphenylboronic acid is a biochemical reagent suitable for life science research. It functions as a substrate in palladium-catalyzed cross-coupling reactions and as a reactant in Suzuki-Miyaura cross-coupling reactions. It is also involved in various organic synthesis applications.
Substrate for palladium-catalyzed cross-coupling with benzylic acetates
Reactant in Suzuki-Miyaura cross-coupling reactions
Involved in intramolecular Friedel-Crafts alkylation for chiral tetralins synthesis
Used for hydroxylation to phenols
Participates in oxidative coupling with alkynes
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Small and Specialty Supplier Partner Small and/or specialty supplier based on Federal laws and SBA requirements. Learn More
2-Biphenylboronic acid is a biochemical reagent that serves as a biological material or organic compound for life science related research.
Used as a substrate in palladium-catalyzed cross-coupling with benzylic acetates to provide diarylmethanes.
Acts as a reactant in Suzuki-Miyaura cross-coupling reactions with arylhalides, dibromovinyl precursors, alkenyl tosylates and mesylates, and quinoline carboxylates.
Involved in intramolecular Friedel-Crafts alkylation for the synthesis of chiral tetralins.
Utilized in hydroxylation to phenols and oxidative coupling with alkynes.
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