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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


KitAlysis - Increasing Catalysis Productivity

Cross-Coupling Guide
Safety & Documentation

Safety Information

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

Articles

Boronic Acids - Aldrich ChemFiles 2007, 7.7, 3.

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 - Chemfiles Volume 4 Article 2

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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