• USA Home
  • 465089 - 3,4-Difluorophenylboronic acid

EMAIL THIS PAGE TO A FRIEND
465089 Sigma-Aldrich

3,4-Difluorophenylboronic acid

≥95%

Synonym: 3,4-Difluorobenzeneboronic acid

Purchase

Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Disubstituted Aryl Boronic Acids,
InChI Key   RMGYQBHKEWWTOY-UHFFFAOYSA-N
assay   ≥95%
mp   305-310 °C (lit.)

Description

Other Notes

Contains varying amounts of anhydride

Packaging

5, 25 g in glass bottle

Application

Reactant involved in:
• Suzuki cross-coupling reactions with aryl and heteroaryl halides
• Oxo directing Liebeskind-Srogl cross-coupling reactions with gem-dihaloolefin-type α-oxo ketene dithioacetals
• Substitution reactions with enyne acetates and carbonates

Safety & Documentation

Safety Information

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

Articles

Arylboronic Acids

We are pleased to present its complete selection of arylboronic acids, the building blocks of the Suzuki coupling experiment. Most arylboronic acids readily undergo dehydration reactions to give a cy...
ChemFiles 2001, 1.1, 5.
Keywords: Building blocks, Coupling reactions, Dehydration reaction, Suzuki coupling

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

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?