• USA Home
  • 473286 - Bis(catecholato)diboron

EMAIL THIS PAGE TO A FRIEND
473286 Aldrich

Bis(catecholato)diboron

97%

Synonym: 2,2′-Bi-1,3,2-benzodioxaborole

Purchase

Properties

Related Categories Boronic Acids and Derivatives, Borylation Reagents, Chemical Synthesis, Organometallic Reagents
InChI Key   WYBQOWXCLDXZNR-UHFFFAOYSA-N
assay   97%
mp   189-196 °C(lit.)

Description

Packaging

1, 5 g in glass bottle

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3
Protocols & Articles

Articles

Boronic Acids

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...
Aldrich ChemFiles 2007, 7.7, 3.
Keywords: Chemfiles, Coupling reactions, Dehydration reaction, Suzuki coupling

Diboron Esters

The following diboron esters are highly versatile reagents that couple with organic triflates2 and halides3 to give the corresponding boronic esters, which are readily converted to arylboronic acids....
Chemfiles Volume 4 Article 2
Keywords: Combinatorial synthesis, Coupling reactions, Suzuki coupling

Ir(I)-Catalyzed C–H Borylation

Arylboronic acids and esters are invaluable tools for the chemical community. These powerful reagents are used for a variety of transformations, most notably the Suzuki-Miyaura cross-coupling reactio...
Josephine Nakhla
Chemfiles Volume 11 Article 1
Keywords: Catalysis, Coupling reactions, Cross couplings, Infrared spectroscopy, Methods, Tools

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?