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521485 Sigma-Aldrich

2-Phenoxyphenylboronic 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   AVOWPOFIQZSVGV-UHFFFAOYSA-N
mp   104-108 °C (lit.)

Description

Application

Reactant for:
• Palladium catalyzed cross-coupling reactions
• Trifluoromethylation via copper-mediated oxidative cross-coupling
• Preparation of biologically and pharmacologically active molecules
• Preparation of pyridazine-based scaffolds as a-helix mimetics

Packaging

10 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
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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