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Tris(dibenzylideneacetone)dipalladium(0)

Base Information Edit
  • Chemical Name:Tris(dibenzylideneacetone)dipalladium(0)
  • CAS No.:51364-51-3
  • Molecular Formula:C51H42O3Pd2
  • Molecular Weight:915.733
  • Hs Code.:28439000
  • European Community (EC) Number:610-654-4,620-687-6,932-667-7
  • Wikipedia:Tris(dibenzylideneacetone)dipalladium(0)
  • Mol file:51364-51-3.mol
Tris(dibenzylideneacetone)dipalladium(0)

Synonyms:tris(dibenzylideneacetone)dipalladium;Tris-DBA

Suppliers and Price of Tris(dibenzylideneacetone)dipalladium(0)
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
  • TRC
  • Tris(dibenzylideneacetone)dipalladium
  • 10g
  • $ 290.00
  • TCI Chemical
  • Tris(dibenzylideneacetone)dipalladium(0) >75.0%(T)
  • 5g
  • $ 412.00
  • TCI Chemical
  • Tris(dibenzylideneacetone)dipalladium(0)
  • 200MG
  • $ 23.00
  • TCI Chemical
  • Tris(dibenzylideneacetone)dipalladium(0) >75.0%(T)
  • 1g
  • $ 83.00
  • Strem Chemicals
  • Tris(dibenzylideneacetone)dipalladium(0)
  • 5g
  • $ 275.00
  • Strem Chemicals
  • Tris(dibenzylideneacetone)dipalladium(0)
  • 1g
  • $ 69.00
  • Strem Chemicals
  • Tris(dibenzylideneacetone)dipalladium(0)
  • 25g
  • $ 1103.00
  • Sigma-Aldrich
  • Tris(dibenzylideneacetone)dipalladium(0) 97%
  • 500g
  • $ 7710.00
  • Sigma-Aldrich
  • Tris(dibenzylideneacetone)dipalladium(0) 97%
  • 100g
  • $ 3130.00
  • Sigma-Aldrich
  • Tris(dibenzylideneacetone)dipalladium(0) 97%
  • 50g
  • $ 1150.00
Total 164 raw suppliers
Chemical Property of Tris(dibenzylideneacetone)dipalladium(0) Edit
Chemical Property:
  • Appearance/Colour:dark purple solid 
  • Melting Point:152-155 °C 
  • Boiling Point:400.7 °C at 760 mmHg 
  • Flash Point:176.2 °C 
  • PSA:51.21000 
  • LogP:10.47090 
  • Storage Temp.:2-8°C 
  • Sensitive.:Air & Moisture Sensitive 
  • Solubility.:Soluble in chlorinated solvents, benzene and THF. 
  • Water Solubility.:insoluble 
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:12
  • Exact Mass:916.12077
  • Heavy Atom Count:56
  • Complexity:272
Purity/Quality:

99% *data from raw suppliers

Tris(dibenzylideneacetone)dipalladium *data from reagent suppliers

Safty Information:
  • Pictogram(s): HarmfulXn 
  • Hazard Codes:Xn 
  • Statements: 20/22-36-40 
  • Safety Statements: 24/25-36/37 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2.C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2.C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2.[Pd].[Pd]
  • Isomeric SMILES:C1=CC=C(C=C1)/C=C/C(=O)/C=C/C2=CC=CC=C2.C1=CC=C(C=C1)/C=C/C(=O)/C=C/C2=CC=CC=C2.C1=CC=C(C=C1)/C=C/C(=O)/C=C/C2=CC=CC=C2.[Pd].[Pd]
  • Description Tris(dibenzylideneacetone) dipalladium (Tris DBA) is used as catalyst for a wide variety of Pd catalyzed reactions including Suzuki coupling, Heck coupling, Negishi coupling, Carroll reaarangement, Trost asymmetric allylic alkylation, Buchwald-Hartwig amination of acryl halides, fluorination of allylic chlorides, arylation of ketones, carbonylation of 1,1-dichloro-1-alkenes, ?-arylation of carboxylic esters, and conversion of aryl and vinyl triflates to aryl and vinyl halides. It is also involved in the synthesis of azepane. Tris DBA is also a novel inhibitor of N-myristoyltransferase-1 with significant antitumor activity.
  • Uses Tris(dibenzylideneacetone)dipalladium is used in the preparation of semiconducting polymers processed from nonchlorinated solvents into high performance thin film transistors. Also used in the synthesis of polymer bulk-heterojunction solar sells as a semiconductor. suzuki reaction A cycloaddition catalyst.
Technology Process of Tris(dibenzylideneacetone)dipalladium(0)

There total 3 articles about Tris(dibenzylideneacetone)dipalladium(0) which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
In acetone; at 40 ℃; for 2h; Temperature; Inert atmosphere;
Guidance literature:
With sodium acetate; In methanol; at 40 ℃; for 3h; Inert atmosphere;
DOI:10.1021/acs.orglett.5b03002
Refernces Edit
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