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565806 Aldrich

4-Acetamidophenylboronic acid

Synonym: 4-Acetamidobenzeneboronic 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   VYEWTHXZHHATTA-UHFFFAOYSA-N
mp   215-220 °C(lit.)

Description

Other Notes

Contains varying amounts of anhydride

Packaging

1, 5 g in glass bottle

Application

Reactant involved in:
• Synthesis of TpI2 kinase inhibitors
• Biological evaluation of modulators of survival motor neuron protein
• Cross-coupling with conjugated dienes or terminal alkenes or diazoesters
• Synthesis of tetrabutylammonium trifluoroborates
• Rhosium-catalyzed cyanation

Price and Availability

Suggested Laboratory Gloves


Laboratory GlovesThis substance has been tested against several types of hand protection for CE compliance. Click below to find the recommended gloves for handling this product.




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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