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567485 Aldrich

3,5-Diformylphenylboronic acid

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Description

Packaging

1 g in glass bottle

Application

Reactant involved in:
• Studies of surface-tension of enzyme inhibitors
• Synthesis of bacteriochlorins
• Studies of the activation parameters for recomination reactions of intramolecular redical pairs
• Reactivity studies with diethanolamine
• Regioselective 15-bromination and functionalization of bacteriochlorins
• Synthesis of multicomponent assemblies of boron-based dendritic nanostructures

Price and Availability


Cross-Coupling Guide
Safety & Documentation

Safety Information

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

Articles

Boronic Acids

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

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