A phosphine-free effective palladium catalyst for aqueous Suzuki-Miyaura Cross-Coupling.
Highlights:
The Suzuki reaction (sometimes to referred to as the Suzuki-Miyaura reaction or "Suzuki Coupling") is an organic reaction that is classified as a coupling reaction where the coupling partners are a boronic acid with a halide catalyzed by a palladium complex.
From the laboratory of Benjamin G. Davis, PhD, University of Oxford.
Part of The Investigator's Annexe program.
Product Type: | Small Molecule |
Name: | Bis(2-amino-4,6-dihydroxypyrimidine)palladium(II) diacetate |
Chemical Formula: | C12H16N6O8Pd |
Molecular Weight: | 478.71 kDa |
Format: | Orange solution |
Purity: | Pd: 10 mM; transition metal impurity <0.1 mM |
Solubility: | Soluble in H2O |
Comments: | 10uL for protein reaction; 2.5mL for 0.25 mol aryl bromide |
Storage: | Room temperature |
Shipped: | Ambient temperature |
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