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597112 Sigma-Aldrich

2-Fluoro-5-methoxyphenylboronic acid

≥95%

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Disubstituted Aryl Boronic Acids,
InChI Key   IPTZOWYBCLEBOE-UHFFFAOYSA-N
assay   ≥95%
mp   194-196 °C (lit.)

Description

Application

Reactant involved in:
• Friedel-Crafts alkylation of hydronaphthalenes
• Suzuki-Miyaura cross-coupling reactions
• Synthesis of 9,10-diarylanthracenes for use as molecular switches
• Cross-coupling with carbazolyl or aryl halides

Packaging

5 g in glass bottle

Other Notes

Contains varying amounts of anhydride

Safety & Documentation

Safety Information

RIDADR 
NONH for all modes of transport
WGK Germany 
3

Documents

Certificate of Analysis

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Protocols & Articles

Articles

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

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