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Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II)

Catalog Number
ACM14267084-2
Product Name
Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II)
Structure
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CAS
14267-08-4
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Synonyms
I14-10025; AC1L4Z7Y; AC1Q1RTB; Palladium, dichloro(N,N,N',N'-tetramethyl-1,2-ethanediamine-N,N')-, (SP-4-2)- (9CI); RL01764; Palladium, dichloro(N,N,N',N'-tetramethylethylenediamine)- (8CI); AKOS015900158; TRA0000186; dichloride;
IUPAC Name
palladium(2+);N,N,N',N'-tetramethylethane-1,2-diamine;dichloride;
Molecular Weight
293.528g/mol
Molecular Formula
C6H16Cl2N2Pd;
Canonical SMILES
CN(C)CCN(C)C.[Cl-].[Cl-].[Pd+2];
InChI
InChI=1S/C6H16N2.2ClH.Pd/c1-7(2)5-6-8(3)4;;;/h5-6H2,1-4H3;2*1H;/q;;;+2/p-2;
InChI Key
FJOUSQLMIDWVAY-UHFFFAOYSA-L;
Complexity
42.5
Covalently-Bonded Unit Count
4
Exact Mass
291.973g/mol
H-Bond Acceptor
4
Heavy Atom Count
11
Monoisotopic Mass
291.973g/mol
Rotatable Bond Count
3
Topological Polar Surface Area
6.5A^2
Application
Dichloro(N,N,N',N'-tetramethylethylenediamine)palladium(II) serves as an essential catalyst for various chemical processes, enhancing the efficiency and selectivity of numerous reactions. Its primary applications include facilitating cross-coupling reactions, which are crucial for forming carbon-carbon bonds, and playing a key role in catalytic reduction reactions. Additionally, this compound is instrumental in the preparation of silyl ethers through the reaction of silicon-hydrogen bonds with alcohols, and it also supports oxidative carbonylation reactions. These capabilities make it a versatile tool in both academic research and industrial applications.
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