[S(R)]-N-[(S)-[2-(Dicyclohexylphosphino)phenyl](5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methyl]-2-methyl-2-propanesulfinamide

95%

Reagent Code: #68858
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CAS Number 2398533-82-7

science Other reagents with same CAS 2398533-82-7

blur_circular Chemical Specifications

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Weight 593.9 g/mol
Formula C₃₇H₅₆NOPS
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description Product Description

This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and other carbon-carbon bond-forming reactions. Its sterically demanding and electronically tunable structure allows for high selectivity and efficiency in producing chiral compounds, which are valuable in pharmaceutical synthesis and fine chemical manufacturing. Additionally, it is employed in the development of catalysts for organic synthesis, enabling the production of complex molecules with precise stereochemical control. Its application is particularly significant in the synthesis of biologically active compounds and intermediates for drug development.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,982.00
inventory 500mg
10-20 days ฿103,275.00
inventory 100mg
10-20 days ฿28,791.00

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[S(R)]-N-[(S)-[2-(Dicyclohexylphosphino)phenyl](5,6,7,8-tetrahydro-5,5,8,8-tetramethyl-2-naphthalenyl)methyl]-2-methyl-2-propanesulfinamide
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This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and other carbon-carbon bond-forming reactions. Its sterically demanding and electronically tunable structure allows for high selectivity and efficiency in producing chiral compounds, which are valuable in pharmaceutical synthesis and fine chemical manufacturing

This chemical is primarily utilized in asymmetric synthesis, particularly as a chiral ligand in transition metal-catalyzed reactions. It plays a crucial role in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and other carbon-carbon bond-forming reactions. Its sterically demanding and electronically tunable structure allows for high selectivity and efficiency in producing chiral compounds, which are valuable in pharmaceutical synthesis and fine chemical manufacturing. Additionally, it is employed in the development of catalysts for organic synthesis, enabling the production of complex molecules with precise stereochemical control. Its application is particularly significant in the synthesis of biologically active compounds and intermediates for drug development.

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