[1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)

Pd 14.5%

  • Product Code: 126706
  Alias:    [1,1'-Bis(diphenylphosphino)ferrocene]palladium dichloride
  CAS:    72287-26-4
Molecular Weight: 731.7 g./mol Molecular Formula: C₃₄H₂₈Cl₂FeP₂Pd
EC Number: MDL Number: MFCD00015757
Melting Point: 275-280 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. Its effectiveness stems from the stability and versatility provided by the ferrocene backbone and the diphenylphosphine ligands, which enhance the catalytic activity of palladium. It is especially valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s ability to facilitate the formation of carbon-carbon and carbon-heteroatom bonds makes it a key tool in modern synthetic chemistry. Additionally, its use in asymmetric catalysis enables the production of enantiomerically pure compounds, which are crucial in drug development and fine chemical manufacturing.
Product Specification:
Test Specification
Assay (Pd%) 13-15
Appearance Red To Dark Brown Powder
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days ฿4,530.00
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5.000 10-20 days ฿16,910.00
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25.000 10-20 days ฿65,370.00
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[1,1'-Bis(diphenylphosphino)ferrocene]dichloropalladium(II)
This chemical is widely used as a catalyst in various organic synthesis reactions, particularly in cross-coupling reactions such as Suzuki-Miyaura and Heck reactions. Its effectiveness stems from the stability and versatility provided by the ferrocene backbone and the diphenylphosphine ligands, which enhance the catalytic activity of palladium. It is especially valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound’s ability to facilitate the formation of carbon-carbon and carbon-heteroatom bonds makes it a key tool in modern synthetic chemistry. Additionally, its use in asymmetric catalysis enables the production of enantiomerically pure compounds, which are crucial in drug development and fine chemical manufacturing.
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