(2S)-1-[(1R)-1-(Dimethylamino)ethyl]-2-(diphenylphosphino)ferrocene

98% 99%ee

  • Product Code: 59664
  CAS:    74311-54-9
Molecular Weight: 441.3 g./mol Molecular Formula: C₂₆H₂₈FeNP
EC Number: MDL Number:
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Density: Storage Condition: room temperature, dry
Product Description: This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, combining ferrocene and phosphine groups, allows it to effectively induce chirality in products, making it valuable in the synthesis of enantiomerically pure compounds. It is commonly applied in hydrogenation, cross-coupling, and carbon-carbon bond-forming reactions, where high enantioselectivity is required. Its use is prominent in pharmaceutical and fine chemical industries for producing chiral intermediates and active pharmaceutical ingredients (APIs) with high optical purity. Additionally, its stability and versatility make it a preferred choice for researchers developing new catalytic processes.
Product Specification:
Test Specification
APPEARANCE yellow powder
PURITY 94.5-100
e.e 98.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days $100.97
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(2S)-1-[(1R)-1-(Dimethylamino)ethyl]-2-(diphenylphosphino)ferrocene
This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, combining ferrocene and phosphine groups, allows it to effectively induce chirality in products, making it valuable in the synthesis of enantiomerically pure compounds. It is commonly applied in hydrogenation, cross-coupling, and carbon-carbon bond-forming reactions, where high enantioselectivity is required. Its use is prominent in pharmaceutical and fine chemical industries for producing chiral intermediates and active pharmaceutical ingredients (APIs) with high optical purity. Additionally, its stability and versatility make it a preferred choice for researchers developing new catalytic processes.
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