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565806 Sigma-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,
Quality Level   100
mp   215-220 °C (lit.)
SMILES string   CC(=O)Nc1ccc(cc1)B(O)O
InChI   1S/C8H10BNO3/c1-6(11)10-8-4-2-7(3-5-8)9(12)13/h2-5,12-13H,1H3,(H,10,11)
InChI key   VYEWTHXZHHATTA-UHFFFAOYSA-N

Description

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

Packaging

1, 5 g in glass bottle

Other Notes

Contains varying amounts of anhydride

Safety & Documentation

Safety Information

Personal Protective Equipment 
RIDADR 
NONH for all modes of transport
WGK Germany 
WGK 3
Flash Point(F) 
Not applicable
Flash Point(C) 
Not applicable
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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