Application

4-Cyanophenylboronic acid can be used as a reactant in:Palladium-catalyzed Suzuki-Miyaura cross-coupling in water.Ruthenium catalyzed direct arylation of benzylic sp³ carbons of acyclic amines with arylboronates.Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids.Ferric perchlorate-promoted reaction of fullerenes with various arylboronic acids to give fullerenyl boronic esters.Phosphine-free Suzuki-Miyaura cross-coupling.Palladacycles as effective catalysts for multicomponent reaction with allylpalladium-intermediates.Chan-Lam-type Cu-catalyzed S-arylation of thiols. Regioselective cross-coupling reactions under modfied Suzuki and Still cross-coupling reactions with copper catalysis.Metal-free biaryl coupling reaction in the presence of dimethyl carbonate as a solvent.Suzuki-type cross-coupling reaction with pentavalent triarylantimony diacetates in the absence of a base.It can also be used to prepare:Himbacine analogs as thrombin receptor antagonists and potential antiplatelet agents.Trisulfonated calixarene upper-rim sulfonamido and their complexation with trimethyllysine epigenetic mark.Antimalarial compounds via Suzuki cross-coupling.Deoxyuridine derivatives.

Reactant involved in: Oxidative hydroxylation Trifluoromethylation 1,4-Addition reactionsPrecursor in the synthesis of inhibitors such as: Tpl2 kinase inhibitors P2X7 antagonists used in the treatment of pain

Other Notes

Contains varying amounts of anhydride

Packaging

1 g in glass bottle

10 g in poly bottle