[S(R)]-N-[(S)-[2-(Di-tert-butylphosphino)phenyl[(2-naphthalenyl)methyl]-2-methyl-2-propanesulfinamide

≥95%

  • Product Code: 236123
  CAS:    2565792-62-1
Molecular Weight: 481.68 g./mol Molecular Formula: C₂₉H₄₀NOPS
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C, avoid light, inert gas storage
Product Description: Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in palladium-catalyzed allylic substitution and cross-coupling reactions. Its steric bulk and well-defined chiral environment enable high enantioselectivity in the synthesis of complex organic molecules, making it valuable in pharmaceutical and fine chemical industries. The tert-butyl and naphthyl groups enhance ligand stability and influence metal coordination geometry, leading to improved catalytic efficiency and stereocontrol. It is especially effective in reactions requiring precise spatial arrangement around the metal center for optimal asymmetric induction.
Sizes / Availability / Pricing:
Size Availability Price Quantity
5mg 10-20 days ฿1,320.00
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25mg 10-20 days ฿5,180.00
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-
100mg 10-20 days ฿16,200.00
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[S(R)]-N-[(S)-[2-(Di-tert-butylphosphino)phenyl[(2-naphthalenyl)methyl]-2-methyl-2-propanesulfinamide
Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations, particularly in palladium-catalyzed allylic substitution and cross-coupling reactions. Its steric bulk and well-defined chiral environment enable high enantioselectivity in the synthesis of complex organic molecules, making it valuable in pharmaceutical and fine chemical industries. The tert-butyl and naphthyl groups enhance ligand stability and influence metal coordination geometry, leading to improved catalytic efficiency and stereocontrol. It is especially effective in reactions requiring precise spatial arrangement around the metal center for optimal asymmetric induction.
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