Bis(dicyclohexylphosphino)methane

97%

  • Product Code: 122294
  Alias:    Bis(dicyclohexylphosphine)methane
  CAS:    137349-65-6
Molecular Weight: 408.58 g./mol Molecular Formula: C₆H₁₁₂PCH₂PC₆H₁₁₂
EC Number: MDL Number: MFCD00143763
Melting Point: 95-102 °C(lit.) Boiling Point:
Density: Storage Condition: room temperature
Product Description: Bis(dicyclohexylphosphino)methane is widely used as a ligand in coordination chemistry and catalysis. It is particularly effective in forming stable complexes with transition metals, such as palladium, platinum, and nickel, which are essential in various catalytic processes. These complexes are often employed in cross-coupling reactions, including Suzuki-Miyaura and Heck reactions, which are crucial for constructing carbon-carbon bonds in organic synthesis. Additionally, its bulky and electron-rich nature enhances selectivity and reactivity in catalytic systems, making it valuable in the production of pharmaceuticals, fine chemicals, and advanced materials. Its application also extends to asymmetric catalysis, where it aids in the synthesis of chiral compounds.
Product Specification:
Test Specification
Melting Point 95-102
Purity 97-100
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.250 10-20 days €112.39
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1.000 10-20 days €358.53
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Bis(dicyclohexylphosphino)methane
Bis(dicyclohexylphosphino)methane is widely used as a ligand in coordination chemistry and catalysis. It is particularly effective in forming stable complexes with transition metals, such as palladium, platinum, and nickel, which are essential in various catalytic processes. These complexes are often employed in cross-coupling reactions, including Suzuki-Miyaura and Heck reactions, which are crucial for constructing carbon-carbon bonds in organic synthesis. Additionally, its bulky and electron-rich nature enhances selectivity and reactivity in catalytic systems, making it valuable in the production of pharmaceuticals, fine chemicals, and advanced materials. Its application also extends to asymmetric catalysis, where it aids in the synthesis of chiral compounds.
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