Tris(dibenzylideneacetone)dipalladium(0),[51364-51-3], Pd2(dba)3, Bis(dibenzylideneacetone)palladium(0)

Tris(dibenzylideneacetone)dipalladium(0),[51364-51-3], Pd2(dba)3, Bis(dibenzylideneacetone)palladium(0)
Tris(dibenzylideneacetone)dipalladium(0),[51364-51-3], Pd2(dba)3, Bis(dibenzylideneacetone)palladium(0)
Tris(dibenzylideneacetone)dipalladium(0),[51364-51-3], Pd2(dba)3, Bis(dibenzylideneacetone)palladium(0)
Tris(dibenzylideneacetone)dipalladium(0),[51364-51-3], Pd2(dba)3, Bis(dibenzylideneacetone)palladium(0)

Tris(dibenzylideneacetone)dipalladium(0),[51364-51-3], Pd2(dba)3,Pd2dba3

Tris(dibenzylideneacetone)dipalladium(0) or Pd2(dba)3 is an organometallic complex based on palladium and dibenzylideneacetone used in organic chemistry. Pd2(dba)3 is used as a source of soluble Pd(0), in particular as a catalyst for various coupling reactions. Examples of reactions using this reagent are the Negishi coupling, Suzuki coupling, Carroll rearrangement, and Trost asymmetric allylic alkylation, as well as Buchwald–Hartwig amination.  Palladium catalyst for chemical coupling  


Identification
Name   Tris(dibenzylideneacetone)dipalladium(0)
Synonym    Tris(dibenzylideneacetone)dipalladium,Pd2dba3, Pd2(dba)3
 
Molecular Structure   CAS # 51364-51-3 (52409-22-0), Tris(dibenzylideneacetone)dipalladium
Molecular Formula   C51H42O3Pd2
Molecular Weight   915.73
CAS Registry Number   51364-51-3 (52409-22-0)
Pd content   23.2%
 Specification   Analytical pure
     
Properties
 
Melting point   152-155 ºC
Water solubility   insoluble;sensitive of air and moisture
Appearance   Purple black powder
     
Safety Data
 
Safety Description   S24/25   
MSDS   Tris(dibenzylideneacetone)dipalladium(0) MSDS.pdf
     
Application
Paraffin asymmetric arylation, cross coupling reaction, carbon and nitrogen bond formation reaction, ketone α arylation, suzuki reaction

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