Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Description:

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder is one of the numerous advanced ceramic materials manufactured by Nanochemazone. Nanochemazone produces too many standard grades when applicable, including Mil Spec (military grade); ACS, Reagent and Technical Grade; Food, Agricultural and Pharmaceutical Grade; Optical Grade, USP and EP/BP (European Pharmacopoeia/British Pharmacopoeia) and follows applicable ASTM testing standards. Typical and custom packaging is available. Additional technical, research and safety (MSDS) information are available. Please request a quote above for more information on lead time and pricing.

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder Related Information:

Storage Conditions: 

Airtight sealed, avoid light and keep dry at room temperature.

Please contact us for customization and price inquiry

Email: contact@nanochemazone.com

Note: We supply different size ranges of Nano and micron as per the client’s requirements and also accept customization in various parameters.

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder (CAS No.52522-40-4)

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder Description

Tris(dibenzylideneacetone)dipalladium(0)-chloroform adduct (often abbreviated as Pd₂(dba)₃·CHCl₃) is an organometallic complex used extensively in organic synthesis. It serves as a precatalyst in a variety of palladium-catalyzed reactions, including C-C coupling reactions such as Suzuki, Heck, and Sonogashira couplings. The presence of chloroform (CHCl₃) in the adduct stabilizes the complex and influences its solubility and reactivity.

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder Specifications 

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder Applications

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder can be used:

– To compose the catalytic system for the preparation of homoallylpalladium complexes.These complexes underwent in situ Stille type cross-coupling with various vinyl tin reagents to afford the cyclized products bearing allyl appendages.
– As palladium source in the asymmetric transformations of 3,4-epoxy-1-butene.
– As a catalyst for the Heck cross-coupling reaction of iodobenzene with styrene.
– As a cyclization catalyst.[1][2]
– As a catalyst for [2+2+2] cycloaddition of didehydrotriphenylenes to the corresponding extended triphenylenes.
– As the catalyst for the carbonylation of b,b-imidoyl iodides to the corresponding imidate esters used, in turn, to prepare cyclic, quaternary amino acids.

Tris(dibenzylideneacetone)dipalladium(0)-Chloroform Adduct Powder Safety Information