Atomfair Palladium(II)chloro-bis(acetonitrile) C4H6Cl2N2Pd

Description Palladium(II)chloro-bis(acetonitrile) (CAS No. 14592-56-4) is a highly versatile organometallic compound with the molecular formula C4H6Cl2N2Pd . This air-stable, crystalline complex is widely utilized in catalysis and organic synthesis due to its excellent reactivity and selectivity. The compound features a palladium(II) center coordinated by two acetonitrile ligands and two chloride anions, making it an ideal precursor for Pd-catalyzed cross-coupling reactions such as Suzuki-Miyaura, Heck, and Stille couplings. Its high purity (>98%) ensures consistent performance in research and industrial applications. Suitable for use in homogeneous catalysis, ligand exchange reactions, and as a Pd source in nanoparticle synthesis, this product is a…

Description

Description

Palladium(II)chloro-bis(acetonitrile) (CAS No. 14592-56-4) is a highly versatile organometallic compound with the molecular formula C4H6Cl2N2Pd. This air-stable, crystalline complex is widely utilized in catalysis and organic synthesis due to its excellent reactivity and selectivity. The compound features a palladium(II) center coordinated by two acetonitrile ligands and two chloride anions, making it an ideal precursor for Pd-catalyzed cross-coupling reactions such as Suzuki-Miyaura, Heck, and Stille couplings. Its high purity (>98%) ensures consistent performance in research and industrial applications. Suitable for use in homogeneous catalysis, ligand exchange reactions, and as a Pd source in nanoparticle synthesis, this product is a must-have for synthetic chemists and materials scientists.

  • CAS No: 14592-56-4
  • Molecular Formula: C4H6Cl2N2Pd
  • Molecular Weight: 259.43
  • Exact Mass: 257.89428
  • Monoisotopic Mass: 257.89428
  • IUPAC Name: acetonitrile;palladium(2+);dichloride
  • SMILES: CC#N.CC#N.[Cl-].[Cl-].[Pd+2]
  • Synonyms: Palladium(II)chloro-bis(acetonitrile), AKOS015900211, B1676

Application

Palladium(II)chloro-bis(acetonitrile) serves as a key catalyst in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds in pharmaceutical and agrochemical synthesis. It is also employed in the preparation of Pd nanoparticles for catalytic and electronic applications. Researchers utilize this compound in ligand screening studies due to its labile acetonitrile groups, which facilitate easy substitution.

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