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Biphenyl-2-boronic acid, 95%, Thermo Scientific Chemicals
Description
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.
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
Specifications
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 |
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