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Sigma-Aldrich

Palladium on barium carbonate

greener alternative

reduced, extent of labeling: 5 wt. % loading

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About This Item

Linear Formula:
Pd
MDL number:
UNSPSC Code:
12141733
eCl@ss:
38191001
PubChem Substance ID:
NACRES:
NA.23

form

solid

reaction suitability

reagent type: catalyst
core: palladium

greener alternative product characteristics

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extent of labeling

5 wt. % loading

greener alternative category

SMILES string

[Pd++].[Ba++].[O-]C([O-])=O.[O-]C([O-])=O

InChI

1S/2CH2O3.Ba.Pd/c2*2-1(3)4;;/h2*(H2,2,3,4);;/q;;2*+2/p-4

InChI key

NFXIBAPFNPIUGD-UHFFFAOYSA-J

Application

Palladium on barium carbonate (5% Pd/BaCO3) is a palladium catalyst that can be used in the cross-coupling reaction of arenediazonium salts with boronic acid at low catalytic loading. It can also be used as a catalyst in the diastereoselective hydrogenations of the imine for the synthesis of chiral trifluoromethyl benzylamines.

Other Notes

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Pictograms

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Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

4.1B - Flammable solid hazardous materials

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Efficient and Practical Cross-Coupling of Arenediazonium Tetrafluoroborate Salts with Boronic Acids Catalyzed by Palladium (0)/Barium Carbonate
Felpin F and Fouquet E
advanced synthesis and catalysis, 350(6), 863-868 (2008)
Synthesis of Chiral Trifluoromethyl Benzylamines by Heterogeneous Catalytic Reductive Amination
Dasgupta S, et al.
Topics in Catalysis, 59(13-14), 1207-1213 (2016)
Efficient and Practical Cross-Coupling of Arenediazonium Tetrafluoroborate Salts with Boronic Acids Catalyzed by Palladium (0)/Barium Carbonate
Felpin F and Fouquet E
Advanced Synthesis & Catalysis, 350(6), 863-868 (2008)

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