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588423 Sigma-Aldrich

Phenethylboronic acid

Synonym: 2-Phenylethaneboronic acid

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Properties

Related Categories Alkyl and Aryl Boronic Acids, Boronic Acids, Boronic Acids and Derivatives, Chemical Synthesis, Organometallic Reagents More...
InChI Key   VPRUMANMDWQMNF-UHFFFAOYSA-N
mp   76-81 °C (lit.)

Description

Application

Reactant involved in:
• Suzuki-Miyaura cross-coupling reactions
• Reactions with α-diazocarbonyl compounds
• C-H functionalization of quinones
• Cross-coupling with aromatic amines
• Arylation and alkylation of diphenylisoxazole

Reactant used in studies of the stability of boronic esters to hydrolysis

Packaging

1, 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

Peer-Reviewed Papers
15

References

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