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445223 Aldrich

2-Fluorophenylboronic acid

Synonym: 2-Fluorobenzeneboronic acid, o-fluoro-benzeneboronic acid

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Monosubstituted Aryl Boronic Acids,
InChI Key   QCSLIRFWJPOENV-UHFFFAOYSA-N
mp   101-110 °C(lit.)

Description

Other Notes

Contains varying amounts of anhydride

Packaging

1, 10 g in glass bottle

Application

Reactant for:
• Preparation of phenylboronic catechol esters as promising anion receptors for polymer electrolytes
• Diastereoselective synthesis of trisubstituted allylic alcohols via rhodium-catalyzed arylation
• Site-selective Suzuki-Miyaura arylation reactions
• Rh-catalyzed enantioselective addition reactions
• Rhodium- and Palladium-catalyzed substitution reactions

Used for the preparation of biologically active biphenyls and arylboron difluoride Lewis acids.

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

Arylboronic Acids

Aldrich is 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 ...
Aldrich ChemFiles 2001, 1.1, 5.
Keywords: Building blocks, Coupling reactions, Dehydration reaction, Suzuki coupling

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

Peer-Reviewed Papers
15

References

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