Allylpalladium(II) chloride dimer, 12012-95-2, C6H10Cl2Pd2
Allylpalladium(II) chloride dimer, 12012-95-2, C6H10Cl2Pd2
Allylpalladium(II) chloride dimer, 12012-95-2, C6H10Cl2Pd2
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Allylpalladium(II) chloride dimer

Identification
Name
Allylpalladium(II) chloride dimer
Synonyms

chloropalladium(1+),prop-1-ene;
Diallyldichlorodipalladium;
Di-μ-chlorobis[(η-allyl)palladium(II)];
[PdCl(allyl)]2;
[PdCl(C3H5)]2;
Bis(allyl)dichloropalladium;
Bis(allyl)dichlorodipalladium;
Allylchloropalladium dimer;
Bis(allylchloropalladium);


Molecular Structure
12012-95-2

Molecular Formula
C6H10Cl2Pd2
Molecular Weight
365.89
CAS Registry Number
12012-95-2
EINECS
234-579-8
Properties
Pd content
58.2% up
Appearance
Yellow crystal
Melting point

120°C
Water solubility
decomposes
Safety Data
Hazard Symbols
Xi
Risk Codes
R36/37/38
Safety Description
S26;S36

Allylpalladium(II) chloride dimer uses:

Used as a catalyst for homogeneous reactions and hydrosilylation.

1. A precatalyst for the enantioselective hydrosilylation of olefins.

2. Pre-catalyst for asymmetric alkylation and amination of cyclopropenyl acetate.

3. Cross-coupling reaction catalyst.

4. Dimers can be used as Trost ligands.

5. As a useful precursor for highly enantioselective allyl alkylation and amination.

6. Alkene stannous alkylation catalyst.

Allylpalladium(II) chloride dimer Advantage:

① Can control the single impurity content

② Purity can be controlled according to customer requirements

Used as a catalyst for the Heck reaction, and also as a catalyst to participate in the tandem nucleophilic allylation-alkoxyallylation reaction of alkynal with allyl chloride and allyl butylstannane.

Product Catalog
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