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Biphenyl-2-boronic acid, 95%, Thermo Scientific Chemicals

Product Code. 15459069
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Quantity:
1 g
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This item is not returnable. View return policy

 

It is a substrate employed in a palladium-catalyzed cross-coupling with benzylic acetates providing diarylmethanes. It is a reactant involved in Suzuki-Miyaura cross-coupling reactions with arylhalides, dibromovinyl precursors, alkenyl tosylates and mesylates, and quinoline carboxylates. It is involved in intramolecular Friedel-Crafts alkylation for synthesis of chiral tetralins, hydroxylation to phenols and oxidative coupling with alkynes.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
It is a substrate employed in a palladium-catalyzed cross-coupling with benzylic acetates providing diarylmethanes. It is a reactant involved in Suzuki-Miyaura cross-coupling reactions with arylhalides, dibromovinyl precursors, alke
TRUSTED_SUSTAINABILITY

Specifications

CAS 4688-76-0
Melting Point 173°C to 194°C
Molecular Formula C12H11BO2
MDL Number MFCD00136929
Quantity 1 g
Beilstein 3031806
Synonym 2-biphenylboronic acid, biphenyl-2-boronic acid, biphenyl-2-ylboronic acid, 2-biphenylboronicacid, 2-phenylphenyl boranediol, 2-phenylphenyl boronic acid, 1,1'-biphenyl-2-ylboronic acid, 2-biphenylylboronic acid, 1,1'-biphenylboronic acid, 2-phenylbenzeneboronic acid
Solubility Information Insoluble in water.
InChI Key HYCYKHYFIWHGEX-UHFFFAOYSA-N
SMILES B(C1=CC=CC=C1C2=CC=CC=C2)(O)O
IUPAC Name (2-phenylphenyl)boronic acid
Molecular Weight (g/mol) 198.028
PubChem CID 4589187
Formula Weight 198.03
Percent Purity 95%
Chemical Name or Material Biphenyl-2-boronic acid
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