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518808 Aldrich

Bis(neopentyl glycolato)diboron

96%

Synonym: 5,5,5′,5′-Tetramethyl-2,2′-bi-1,3,2-dioxaborinane

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Properties

Related Categories Boronic Acids and Derivatives, Borylation Reagents, Chemical Synthesis, Organometallic Reagents
InChI Key   MDNDJMCSXOXBFZ-UHFFFAOYSA-N
assay   96%
mp   180.5-184.5 °C(lit.)

Description

Application

Reagent to prepare boronic acid esters.

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

Peer-Reviewed Papers
15

References

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