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(Ethylenediamine)palladium(II) chloride

Catalog Number
ACM15020992-3
Product Name
(Ethylenediamine)palladium(II) chloride
Structure
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CAS
15020-99-2
  • Product Overview
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Synonyms
Dichloro(1,2-diaminoethane)palladium; Dichloro(ethylenediamine)palladium(II); C2H8Cl2N2Pd; (Ethylenediamine)palladium(II) chloride; 7518AA; NSC 209490; (Ethylenediamine)palladium(II) chloride, >=99.99%; Dichloro(ethylenediamine)palladium(II), Pd 44.8%; MFCD00044991;
IUPAC Name
dichloropalladium;ethane-1,2-diamine;
Molecular Weight
237.42g/mol
Molecular Formula
C2H8Cl2N2Pd;
Canonical SMILES
C(CN)N.Cl[Pd]Cl;
InChI
InChI=1S/C2H8N2.2ClH.Pd/c3-1-2-4;;;/h1-4H2;2*1H;/q;;;+2/p-2;
InChI Key
CAYKJANQVKIYPJ-UHFFFAOYSA-L;
Complexity
8.8
Covalently-Bonded Unit Count
2
Exact Mass
235.91g/mol
H-Bond Acceptor
2
H-Bond Donor
2
Heavy Atom Count
7
Monoisotopic Mass
235.91g/mol
Rotatable Bond Count
1
Topological Polar Surface Area
52A^2
Application
(Ethylenediamine)palladium(II) chloride serves as a versatile catalyst and reactant in various chemical reactions and complex formations. Primarily, it plays a critical role in C-C coupling reactions, such as the Sonogashira coupling, which is integral to the synthesis of 6-(substituted benzyl)imidazo[2,1-b][1,3]thiazole. Additionally, it facilitates the formation of host-guest complexes and is essential for the self-assembly of intricate ring-in-ring structures. This compound also aids in metal binding with glycose phosphates and is key in the synthesis of mixed-metal, mixed-pyrimidine self-assembling metallacalix[n]arenes, showcasing its multifaceted utility in advanced chemical synthesis and materials science.
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