![3375-31-3 | Palladium(II) Acetate | Palladium(2+) Acetic Acid Salt; Palladium Acetic Acid Salt; Bis(Acetato)palladium; Diacetatopalladium; Diacetoxypalladium; HyCat 1; HyCat Base 1; Palladium Diacetate; Palladous Acetate; | (C₂H₃O₂)₂Pd | TRC 3375-31-3 | Palladium(II) Acetate | Palladium(2+) Acetic Acid Salt; Palladium Acetic Acid Salt; Bis(Acetato)palladium; Diacetatopalladium; Diacetoxypalladium; HyCat 1; HyCat Base 1; Palladium Diacetate; Palladous Acetate; | (C₂H₃O₂)₂Pd | TRC](https://www.trc-canada.com/prod-img/P141105.png)
3375-31-3 | Palladium(II) Acetate | Palladium(2+) Acetic Acid Salt; Palladium Acetic Acid Salt; Bis(Acetato)palladium; Diacetatopalladium; Diacetoxypalladium; HyCat 1; HyCat Base 1; Palladium Diacetate; Palladous Acetate; | (C₂H₃O₂)₂Pd | TRC
![Palladium-Catalyzed Carbohalogenation: Bromide to Iodide Exchange and Domino Processes | Journal of the American Chemical Society Palladium-Catalyzed Carbohalogenation: Bromide to Iodide Exchange and Domino Processes | Journal of the American Chemical Society](https://pubs.acs.org/cms/10.1021/ja206099t/asset/images/medium/ja-2011-06099t_0008.gif)
Palladium-Catalyzed Carbohalogenation: Bromide to Iodide Exchange and Domino Processes | Journal of the American Chemical Society
![SOLVED: A palladium complex formed from a solution containing bromide ion and pyridine, C5H5N (a good electron-pair donor), is found on elemental analysis to contain 37.6% bromine, 28.3% carbon, 6.60% nitrogen, and SOLVED: A palladium complex formed from a solution containing bromide ion and pyridine, C5H5N (a good electron-pair donor), is found on elemental analysis to contain 37.6% bromine, 28.3% carbon, 6.60% nitrogen, and](https://cdn.numerade.com/ask_previews/181b85e5-50b3-41e0-8bff-8910f9854798_large.jpg)
SOLVED: A palladium complex formed from a solution containing bromide ion and pyridine, C5H5N (a good electron-pair donor), is found on elemental analysis to contain 37.6% bromine, 28.3% carbon, 6.60% nitrogen, and
Aryl bromide/triflate selectivities reveal mechanistic divergence in palladium-catalysed couplings; the Suzuki–Miyaura anomaly - Chemical Communications (RSC Publishing)
![Palladium-catalyzed allene synthesis enabled by β-hydrogen elimination from sp2-carbon | Nature Communications Palladium-catalyzed allene synthesis enabled by β-hydrogen elimination from sp2-carbon | Nature Communications](https://media.springernature.com/full/springer-static/image/art%3A10.1038%2Fs41467-020-20740-w/MediaObjects/41467_2020_20740_Fig1_HTML.png)
Palladium-catalyzed allene synthesis enabled by β-hydrogen elimination from sp2-carbon | Nature Communications
![Palladium(II) bromide, Premion , 99.998% (metals basis), Pd 39.5% min, Thermo Scientific Chemicals, Quantity: 1 g | Fisher Scientific Palladium(II) bromide, Premion , 99.998% (metals basis), Pd 39.5% min, Thermo Scientific Chemicals, Quantity: 1 g | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/CCG/logos/Thermo-Scientific-Stacked.jpg-250.jpg)
Palladium(II) bromide, Premion , 99.998% (metals basis), Pd 39.5% min, Thermo Scientific Chemicals, Quantity: 1 g | Fisher Scientific
![Base-free efficient palladium catalyst of Heck reaction in molten tetrabutylammonium bromide - ScienceDirect Base-free efficient palladium catalyst of Heck reaction in molten tetrabutylammonium bromide - ScienceDirect](https://ars.els-cdn.com/content/image/1-s2.0-S1381116906007151-fx1.gif)
Base-free efficient palladium catalyst of Heck reaction in molten tetrabutylammonium bromide - ScienceDirect
![Palladium(II) bromide, Premion , 99.99% (metals basis), Pd 39.5% min, Thermo Scientific Chemicals, Quantity: 2 g | Fisher Scientific Palladium(II) bromide, Premion , 99.99% (metals basis), Pd 39.5% min, Thermo Scientific Chemicals, Quantity: 2 g | Fisher Scientific](https://assets.fishersci.com/TFS-Assets/CCG/Chemical-Structures/chemical-structure-cas-12135-22-7.jpg-650.jpg)