(R)-N-((S)-2-(Diphenylphosphanyl)-1-(2',4',6'-triisopropyl-[1,1'-biphenyl]-2-yl)ethyl)-2-methylpropane-2-sulfinamide

97%

Reagent Code: #231333
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CAS Number 2394923-81-8

science Other reagents with same CAS 2394923-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 611.9 g/mol
Formula C₃₉H₅₀NOPS
badge Registry Numbers
MDL Number MFCD32697171
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its steric bulk and well-defined chiral environment enable high enantioselectivity in the synthesis of complex organic molecules, including pharmaceuticals and natural products. It is particularly effective in ruthenium- or rhodium-catalyzed asymmetric hydrogenations, where it helps generate chiral centers with high optical purity. Due to its modular structure, it is also employed in the development of new catalytic systems for stereoselective C–C and C–heteroatom bond formations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿4,200.00
100mg
10-20 days ฿13,080.00
(R)-N-((S)-2-(Diphenylphosphanyl)-1-(2',4',6'-triisopropyl-[1,1'-biphenyl]-2-yl)ethyl)-2-methylpropane-2-sulfinamide
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its steric bulk and well-defined chiral environment enable high enantioselectivity in the synthesis of complex organic molecules, including pharmaceuticals and natural products. It is particularly effective in ruthenium- or rhodium-catalyzed asymmetric hydrogenations, where it helps generate chiral centers with high optical purity.

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its steric bulk and well-defined chiral environment enable high enantioselectivity in the synthesis of complex organic molecules, including pharmaceuticals and natural products. It is particularly effective in ruthenium- or rhodium-catalyzed asymmetric hydrogenations, where it helps generate chiral centers with high optical purity. Due to its modular structure, it is also employed in the development of new catalytic systems for stereoselective C–C and C–heteroatom bond formations.

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