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441635 Aldrich

3-Ethoxyphenylboronic acid

Synonym: 3-Ethoxybenzeneboronic 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   CHCWUTJYLUBETR-UHFFFAOYSA-N
impurities   <15% anhydride
mp   139-146 °C(lit.)

Description

Packaging

1 g in glass bottle

Application

Reactant involved in:
• Cyanation for synthesis of aromatic and vinyl nitriles
• Microwave-assisted palladium-catalyzed arylation of resin supported pyrazinones
• Copper-mediated N- and O-arylations

Reactant involved in synthesis of biologically active molecules including:
• Amino derivatives of indole for use as isoprenylcysteine carboxyl methyltransferase inhibitors
• 5-Arylindazole glucocorticoid receptor agonists and antagonists
• 1,5-Diaryl-1,2,4-triazoles as cis-restricted combretastatin analogs

Price and Availability

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

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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