[S(R)]-N-[(S)-[2-(Diphenylphosphino)phenyl]phenylmethyl]-N,2-dimethyl-2-propanesulfinamide

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Reagent Code: #68864
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CAS Number 2565792-25-6

science Other reagents with same CAS 2565792-25-6

blur_circular Chemical Specifications

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Weight 485.6 g/mol
Formula C₃₀H₃₂NOPS
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description Product Description

This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in transition metal-catalyzed reactions. It plays a critical role in facilitating enantioselective transformations, such as hydrogenations, cross-coupling reactions, and other processes where the creation of chiral centers is essential. Its unique structure, featuring a diphenylphosphino group and sulfinamide moiety, allows it to effectively coordinate with metals like rhodium, palladium, or iridium, enabling high stereocontrol in the synthesis of complex organic molecules. This makes it valuable in the pharmaceutical industry for producing enantiomerically pure drugs and intermediates. Additionally, it is employed in academic research to explore new methodologies in asymmetric catalysis.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,005.00
inventory 100mg
10-20 days ฿6,480.00

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[S(R)]-N-[(S)-[2-(Diphenylphosphino)phenyl]phenylmethyl]-N,2-dimethyl-2-propanesulfinamide
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This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in transition metal-catalyzed reactions. It plays a critical role in facilitating enantioselective transformations, such as hydrogenations, cross-coupling reactions, and other processes where the creation of chiral centers is essential. Its unique structure, featuring a diphenylphosphino group and sulfinamide moiety, allows it to effectively coordinate with metals like rhodium, palladium, or iridium,

This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand or catalyst in transition metal-catalyzed reactions. It plays a critical role in facilitating enantioselective transformations, such as hydrogenations, cross-coupling reactions, and other processes where the creation of chiral centers is essential. Its unique structure, featuring a diphenylphosphino group and sulfinamide moiety, allows it to effectively coordinate with metals like rhodium, palladium, or iridium, enabling high stereocontrol in the synthesis of complex organic molecules. This makes it valuable in the pharmaceutical industry for producing enantiomerically pure drugs and intermediates. Additionally, it is employed in academic research to explore new methodologies in asymmetric catalysis.

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