Application

4-(Trifluoromethyl)phenylboronic acid can be used as a reactant in:Site-selective Suzuki-Miyaura cross-coupling reactions.Palladium-catalyzed direct arylation reactions.Tandem-type Pd(II)-catalyzed oxidative Heck reaction and intramolecular C-H amidation sequence.Ruthenium catalyzed direct arylation.Ligand-free copper-catalyzed coupling reactions.Amination and conjugate addition reactions.Regioselective arylation and alkynylation by Suzuki-Miyaura and Sonogashira cross-coupling reactions.Rhodium-catalyzed asymmetric 1,4-addition reactions.Copper-catalyzed nitration reactions.Regioselective Suzuki-Miyaura coupling and tandem palladium-catalyzed intramolecular aminocarbonylation and annulation.Palladium catalyzed allylation reaction with allyl alcohols.N-Arylation of imidazoles and amines in the presence of copper-exchanged fluorapatite as a catalyst.It can also be used as a reactant to prepare:Thiazole derivatives for printable electronics.Terphenyl benzimidazoles as tubulin polymerization inhibitors. Aryl ketones by cross-coupling reaction with acid chlorides.

Other Notes

Contains varying amounts of anhydride

Packaging

1, 5 g in glass bottle