858971-43-4

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858971-43-4 Structure

Identification	Back Directory
[Name] 1,2-Bis(phenylsulfinyl)ethanepalladium(II)acetate,min.98%ChristinaWhiteCatalyst
[CAS] 858971-43-4
[Synonyms] White Catalyst 1,2-Bis(phenylsulfinyl)ethane-palladium diacetate 1,2-Bis(phenylsulfinyl)ethane palladium(II) acetate 1,2-Bis(phenylsulfinyl)ethane Palladium(II) Diacetate 1,2-Bis(phenylsulfinyl)ethanepalladium(II) acetate, min. 98% 1,2-Bis(phenylsulfinyl)ethanepalladium(II) acetate,Christina White Catalyst,98% 1,2-Bis(phenylsulfinyl)ethanepalladium(II)acetate,min.98%ChristinaWhiteCatalyst 1,2-Bis(phenylsulfinyl)ethanepalladiuM(II) acetate,98% Christina White Catalyst
[Molecular Formula] C14H14O2S2.C4H6O4Pd
[MDL Number] MFCD09842752
[MOL File] 858971-43-4.mol
[Molecular Weight] 502.902

Chemical Properties	Back Directory
[storage temp. ] Freezer
[solubility ] soluble in Chloroform
[form ] Powder
[color ] orange to brown
[Stability:] store cold

Questions And Answer	Back Directory
[Reaction] Catalyst for allylic oxidation. Catalyst for oxidative Heck reactions. Catalyst for allylic alkylation. Catalyst for allylic amination.

Hazard Information	Back Directory
[Uses] Macrolactonization via Hydrocarbon Oxidation
[Uses] Efficient bis-sulfoxide-Pd(II) catalyst for intramolecular allylic C–H oxidation, sequential allylic C–H oxidation/vinylic C–H arylation, and allylic C–H amination.
[General Description] This product has been enhanced for catalytic efficiency.
[reaction suitability] core: palladium reaction type: Buchwald-Hartwig Cross Coupling Reaction reaction type: Cross Couplings reaction type: Heck Reaction reaction type: Hiyama Coupling reaction type: Negishi Coupling reaction type: Sonogashira Coupling reaction type: Stille Coupling reaction type: Suzuki-Miyaura Coupling reagent type: catalyst reaction type: C-H Activation

Spectrum Detail	Back Directory
[Spectrum Detail] 1,2-Bis(phenylsulfinyl)ethanepalladium(II)acetate,min.98%ChristinaWhiteCatalyst(858971-43-4)¹HNMR

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