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557234 Sigma-Aldrich

5-Chloro-2-fluorophenylboronic acid

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Properties

Related Categories Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Disubstituted Aryl Boronic Acids,
InChI Key   GGTUVWGMCFXUAS-UHFFFAOYSA-N
mp   122-127 °C (lit.)

Description

Application

Reactant involved in:
• Suzuki cross-coupling reactions
• Synthesis of biaryl amides with muscarinic acetylcholine receptor subtype M1 agonistic activity
• Synthesis of kinesin spindle protein inhibitors
• GABA α2/3 agonist preparation

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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