Purpose:Tri (dibenzalacetone) dipalladium (0) is an important zero-valent palladium catalyst, which is widely used in coupling, hydrogenation, carbonylation and other reactions in organic synthesis. In combination with different ligands of Chemicalbook, high catalytic activity of zero-valent palladium active substance is formed in situ, which has been widely used in carbon-carbon bond and carbon-heteroatomic bond formation reactions.
Aryl chloride Suzuki coupling reaction catalyst; Aryl chloride Heck coupling reaction catalyst; Ketone arylation catalyst; Buchwald-Hartwig catalyst for amination reaction of aryl halide; Alkene Chemicalbook propyl chloride fluorination catalyst; Carboxylate β-arylation catalyst; 1, 1-dichloro-1-olefin carbonylation catalyst; Catalyst for conversion of aryl and vinyl trifluoromesylate to aryl and vinyl halides
Scope of application:It has high catalytic activity in the coupling reaction of chlorinated aromatics and phenylboric acid. It can also be used for Stille coupling between chlorinated aromatics and organotin, Heck cross-coupling reaction between chlorinated aromatics and olefin, Chemicalbook and catalytic asymmetric Heck arylation reaction of olefin within the molecule. This kind of reaction has a wide range of applications in the synthesis of polymers, liquid crystal materials, functional materials, drugs and bioactive compounds.
| Point of melting: |
152-155°C |
| Storage conditions: |
2-8°C |
| Degree of solubility: |
Soluble in chlorinated solvents, benzene and THF. |
| Solubility of water: |
insoluble |
| sensibility |
Air & Moisture Sensitive |
| Customs code |
28439000 |
Audited Supplier 
Audited Supplier 
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