• USA Home
  • 542202 - 2-Biphenylboronic acid

EMAIL THIS PAGE TO A FRIEND
542202 Sigma-Aldrich

2-Biphenylboronic acid

≥95%

Purchase

Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   HYCYKHYFIWHGEX-UHFFFAOYSA-N
assay   ≥95%
mp   167-172 °C (lit.)

Description

Application

Reactant involved in:
• Suzuki-Miyaura cross-coupling reactions with arylhalides, dibromovinyl precursors, alkenyl tosylates and mesylates, and quinoline carboxylates
• Intramolecular Friedel-Crafts alkylation for synthesis of chiral tetralins
• Hydroxylation to phenols
• Oxidative coupling iwth alkynes

Substrate employed in a palladium-catalyzed cross-coupling with benzylic acetates providing diarylmethanes.

Packaging

5 g in glass bottle

Other Notes

Contains varying amounts of anhydride.

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

Please Enter a Lot Number
Protocols & Articles

Articles

Boronic Acids - ChemFiles 2007

Most boronic acids readily undergo dehydration reactions to give a cyclic (trimer) anhydride. Our selection of boronic acids may contain varying amounts of this cyclic anhydride. Fortunately, the aci...
ChemFiles 2007, 7.7, 3.
Keywords: Coupling reactions, Dehydration reaction, Suzuki coupling

Peer-Reviewed Papers
15

References

Related Products

Technical Service:

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Bulk Ordering & Pricing:

Need larger quantities for your development, manufacturing or research applications?