[S(R)]-N-[(1S)-1-[5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]-2,2-dimethylpropyl]-2-methyl-2-propanesulfinamide

95%

  • Product Code: 65030
  CAS:    2162939-89-9
Molecular Weight: 583.8 g./mol Molecular Formula: C₃₆H₄₂NO₂PS
EC Number: MDL Number: MFCD32697192
Melting Point: Boiling Point:
Density: Storage Condition: room temperature, inert gas
Product Description: This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, featuring a xanthene backbone and a sulfinamide group, provides excellent steric and electronic control, enabling high selectivity and yield in the synthesis of chiral molecules. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where precise stereochemistry is essential. Additionally, its stability and compatibility with various reaction conditions make it a versatile tool in organic synthesis.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.005 10-20 days $70.43
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0.025 10-20 days $318.19
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0.100 10-20 days $919.87
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[S(R)]-N-[(1S)-1-[5-(Diphenylphosphino)-9,9-dimethyl-9H-xanthen-4-yl]-2,2-dimethylpropyl]-2-methyl-2-propanesulfinamide
This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its unique structure, featuring a xanthene backbone and a sulfinamide group, provides excellent steric and electronic control, enabling high selectivity and yield in the synthesis of chiral molecules. This makes it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals where precise stereochemistry is essential. Additionally, its stability and compatibility with various reaction conditions make it a versatile tool in organic synthesis.
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