(S)-1-((Rp)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenyl)ethyldi-tert-butylphosphine

98%

  • Product Code: 70438
  CAS:    849924-40-9
Molecular Weight: 658.61 g./mol Molecular Formula: C₃₈H₅₂FeO₂P₂
EC Number: MDL Number: MFCD08561157
Melting Point: Boiling Point:
Density: Storage Condition: room temperature
Product Description: This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, combining ferrocene and phosphine groups, provides excellent steric and electronic control, leading to high enantiomeric excess in the synthesis of chiral molecules. This makes it valuable in the pharmaceutical industry for producing enantiomerically pure drugs and intermediates. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore asymmetric synthesis pathways.
Product Specification:
Test Specification
Purity 97.5 100%
Appearance Orange powder
Infrared spectrum Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿6,680.00
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(S)-1-((Rp)-2-[Bis(4-methoxy-3,5-dimethylphenyl)phosphino]ferrocenyl)ethyldi-tert-butylphosphine
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, combining ferrocene and phosphine groups, provides excellent steric and electronic control, leading to high enantiomeric excess in the synthesis of chiral molecules. This makes it valuable in the pharmaceutical industry for producing enantiomerically pure drugs and intermediates. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore asymmetric synthesis pathways.
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