Tris(dibenzylideneacetone)dipalladium(0), 97%

Not available outside of the UK & Ireland.

Application

Catalyst for Suzuki coupling of aryl chlorides (eq. 1)Catalyst for Heck coupling of aryl chlorides (eq. 2)Catalyst for arylation of ketones (eq. 3)Catalyst for Buchwald-Hartwig amination of aryl halides (eq. 4)Catalyst for fluorination of allylic chlorides (eq. 5)Catalyst for β-arylation of carboxylic esters (eq. 6)Catalyst for carbonylation of 1,1-dichloro-1-alkenes (eq. 7)Catalyst for conversion of aryl and vinyl triflates to aryl and vinyl halides (eq. 8)

Application Guide for Palladium Catalyzed Cross-Coupling ReactionsReactant involved in: Synthesis of nanosized palladium phosphides upon interaction with white phosphorous Preparation of palladium triphenylphosphine carbonyl cluster complexes Precursor for synthesis of functionalized multiwalled carbon nanotube-palladium complexes used as catalysts for Heck coupling reactions Selective carbon-sulfur bond formation via addition of S-S and S-H bonds to alkynesCatalyst for: Suzuki cross-coupling reactions PCN- and PCS-pincer palladium complex catalyzed tandem allylation

General description

Tris(dibenzylideneacetone)dipalladium(0) (Pd₂(dba)₃) participates in the synthesis of azepane. Crystal structure of Pd₂(dba)₃ has been determined by three-dimensional X-ray data. Crystals of Pd₂(dba)₃ are reported to crystalize in triclinic system. It is widely used Pd(0) source in Pd-mediated transformations.

Packaging

1, 5, 25, 50, 100, 500 g in glass bottle

500 mg in glass bottle