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Medchemexpress LLC Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct | 95464-05-4 | 98.5% | 816.64 | 5 G
SDP

Catalog No. 5000402622
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Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct is a common dichloromethane solvate of the palladium catalyst Pd(dppf)Cl2. This phosphine ligand palladium(II) complex serves as a versatile precatalyst for various cross-coupling reactions, capable of stabilizing reaction intermediates and lowering activation energy, making it suitable for Suzuki-Miyaura coupling reaction studies. In vitro, it efficiently catalyzes diverse cross-coupling reactions and can modify complex bioactive molecules containing free amino groups without requiring catalyst changes.

  • Stabilizes reaction intermediates
  • Lowers reaction activation energy
  • Suitable for Suzuki-Miyaura coupling reaction studies
  • Efficiently catalyzes various cross-coupling reactions
  • Modifies complex bioactive molecules containing free amino groups
  • Product can be purified by column chromatography after reaction

Catalog No. 50-004-02622 Supplier Medchemexpress LLC Supplier No. HY216235G
May include imposed supplier surcharges.
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Dichloro[1,1'-bis(diphenylphosphino)ferrocene]palladium(II) dichloromethane adduct is a common dichloromethane solvate of the palladium catalyst Pd(dppf)Cl2. This phosphine ligand palladium(II) complex serves as a versatile precatalyst for various cross-coupling reactions, capable of stabilizing reaction intermediates and lowering activation energy, making it suitable for Suzuki-Miyaura coupling reaction studies. In vitro, it efficiently catalyzes diverse cross-coupling reactions and can modify complex bioactive molecules containing free amino groups without requiring catalyst changes.

  • Stabilizes reaction intermediates
  • Lowers reaction activation energy
  • Suitable for Suzuki-Miyaura coupling reaction studies
  • Efficiently catalyzes various cross-coupling reactions
  • Modifies complex bioactive molecules containing free amino groups
  • Product can be purified by column chromatography after reaction

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