[S(R)]-N-[(1S)-1-(2',6'-Diisopropyl)-(1,1'-biphenyl)-2-yl]-2-(diphenylphosphino)ethyl]-2-methyl-2-propanesulfinamide

≥95%

Reagent Code: #65015
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CAS Number 2394923-85-2

science Other reagents with same CAS 2394923-85-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 569.79 g/mol
Formula C₃₆H₄₄NOPS
badge Registry Numbers
MDL Number MFCD32697175
inventory_2 Storage & Handling
Storage room temperature, inert gas

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It plays a significant role in the formation of carbon-carbon and carbon-heteroatom bonds, making it valuable in the production of pharmaceuticals and fine chemicals. Its application extends to transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution, where it helps achieve precise stereochemical control. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and biologically active compounds, where the stereochemistry of the product is critical for its function.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿1,701.00
inventory 25mg
10-20 days ฿7,641.00
inventory 100mg
10-20 days ฿21,591.00

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[S(R)]-N-[(1S)-1-(2',6'-Diisopropyl)-(1,1'-biphenyl)-2-yl]-2-(diphenylphosphino)ethyl]-2-methyl-2-propanesulfinamide
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This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It plays a significant role in the formation of carbon-carbon and carbon-heteroatom bonds, making it valuable in the production of pharmaceuticals and fine chemicals. Its application extends to transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution, where it helps achieve precise stereochemical control. A
This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It plays a significant role in the formation of carbon-carbon and carbon-heteroatom bonds, making it valuable in the production of pharmaceuticals and fine chemicals. Its application extends to transition metal-catalyzed reactions, such as hydrogenation, cross-coupling, and allylic substitution, where it helps achieve precise stereochemical control. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and biologically active compounds, where the stereochemistry of the product is critical for its function.
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