Description General description Palladium(II) chloride (PdCl2) reacts with unsubstituted or alkyl-substituted cyclic ketones in the CO atmosphere to afford acyclic diesters and acyclic chloro-substituted monoesters. PdCl2 reacts with N,N-dimethylallylamine in methanol to afford di-μ-chloro-bis(2-methoxy-3-N,N-dimethylaminopropyl)dipalladium(II). Palladium dichloride, acetate and acetylacetonate in the [bmim][BF4] or [bmim][PF6] (where[bmim]+ = 1-butyl-3-methylimidazolium cation) ionic liquids have been employed for the hydrodimerization of butadiene to form octa-2,7-dien-1-ol. Application Application Guide for Palladium Catalyzed Cross-Coupling Reactions Used in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar. Palladium(II) chloride (PdCl2) was used in the following studies: • As catalyst for the carbonylation of organic tellurides by reaction with carbon monoxide. • As a catalyst along with Cu(II) for the deamination of phenethylamines to phenyl substituted pyrroles. • Together with PEG 300, promoted efficient Suzuki-coupling of aryl chlorides with aryl boronic acids. Packaging 1, 5, 25, 100 g in glass bottle