(1R)-1-(Dicyclohexylphosphino)-2-[(S)-[2-(dicyclohexylphosphino)phenyl](dimethylamino)methyl]ferrocene

98%

  • Product Code: 230634
  CAS:    914089-00-2
Molecular Weight: 711.76 g./mol Molecular Formula: C₄₃H₆₃FENP₂
EC Number: MDL Number: MFCD04117706
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective hydrogenation reactions. It is particularly effective in the synthesis of chiral amines, amino acids, and other fine chemicals where high enantiomeric excess is required. Its ferrocene backbone provides structural rigidity and stability, while the phosphine groups coordinate efficiently with transition metals like rhodium and ruthenium, enhancing catalytic activity. Due to its tunable stereochemistry, it supports the development of pharmaceutical intermediates and agrochemicals where precise stereocontrol is critical. The ligand’s performance in homogeneous catalysis makes it valuable in both academic research and industrial processes focused on asymmetric synthesis.
Sizes / Availability / Pricing:
Size Availability Price Quantity
250mg 10-20 days Ft83,527.55
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-
1g 10-20 days Ft333,803.10
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-
(1R)-1-(Dicyclohexylphosphino)-2-[(S)-[2-(dicyclohexylphosphino)phenyl](dimethylamino)methyl]ferrocene
Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective hydrogenation reactions. It is particularly effective in the synthesis of chiral amines, amino acids, and other fine chemicals where high enantiomeric excess is required. Its ferrocene backbone provides structural rigidity and stability, while the phosphine groups coordinate efficiently with transition metals like rhodium and ruthenium, enhancing catalytic activity. Due to its tunable stereochemistry, it supports the development of pharmaceutical intermediates and agrochemicals where precise stereocontrol is critical. The ligand’s performance in homogeneous catalysis makes it valuable in both academic research and industrial processes focused on asymmetric synthesis.
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