4-CYANOPHENYLBORONIC ACID >=95% (C005B-013234)

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.

• 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 reactions

• Tpl2 kinase inhibitors
• P2X7 antagonists used in the treatment of pain

Other Notes

Contains varying amounts of anhydride

UPC:

51284803

Condition:

New

Weight:

1.00 Ounces

HazmatClass:

No

Quantity:

1

Unit of Measurement:

GR

MPN:

521418-1G

CAS:

126747-14-6