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(2-Methylallyl)palladium(II) chloride dimer

Catalog Number
ACM12081184-2
Product Name
(2-Methylallyl)palladium(II) chloride dimer
Structure
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CAS
12081-18-4
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Synonyms
Chloro(2-methylallyl)palladium(II) dimer
IUPAC Name
dichloropalladium; 2-methanidylprop-1-ene; palladium(2+)
Molecular Weight
393.94
Molecular Formula
[CH2=C(CH3)CH2PdCl]2
InChI Key
CZAHDNZKZMLMCE-UHFFFAOYSA-L
Melting Point
168.2-174.0ºC
Purity
0.99
Appearance
yellow powder
Storage
2-8°C
Exact Mass
501.96400
H-Bond Acceptor
4
H-Bond Donor
0
MDL Number
MFCD08561141
Symbol
GHS07
Application
(2-Methylallyl)palladium(II) chloride dimer serves as a versatile catalyst employed in various chemical reactions. It plays a critical role in facilitating asymmetric allylic alkylation reactions, which are essential for the synthesis of chiral compounds. Additionally, it is effective in Suzuki-Miyaura reactions, enabling the formation of carbon-carbon bonds important for constructing complex organic molecules. This compound also catalyzes reductive cleavage reactions, assisting in the breakdown and transformation of chemical structures. Furthermore, it is utilized in the reaction of alkenyloxiranes with carbon monoxide, contributing to the development of advanced molecular frameworks. Overall, (2-Methylallyl)palladium(II) chloride dimer is integral to diverse synthetic processes in organic chemistry.
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