Bis(dicyclohexylphosphino)methane
97%
- Product Code: 122294
Alias:
Bis(dicyclohexylphosphine)methane
CAS:
137349-65-6
Molecular Weight: | 408.58 g./mol | Molecular Formula: | C₆H₁₁₂PCH₂PC₆H₁₁₂ |
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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 |
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Melting Point | 95-102 |
Purity | 97-100 |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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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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