N-((11bR)-2,6-Di([1,1':3',1''-terphenyl]-5'-yl)-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-1,1,1-trifluoromethanesulfonamide

95%

Reagent Code: #215961
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CAS Number 2152685-54-4

science Other reagents with same CAS 2152685-54-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 935.94 g/mol
Formula C₅₇H₃₇F₃NO₅PS
inventory_2 Storage & Handling
Density 1.46±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a highly selective ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as palladium-catalyzed cross-couplings and enantioselective transformations. Its sterically demanding and electron-rich structure enhances catalytic efficiency and enantiocontrol. Commonly employed in the synthesis of chiral pharmaceuticals and fine chemicals where high enantiomeric excess is required. Also utilized in advanced materials research due to its rigid aromatic framework and stability under harsh reaction conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿11,340.00
100mg
10-20 days ฿18,130.00
250mg
10-20 days ฿30,800.00
N-((11bR)-2,6-Di([1,1':3',1''-terphenyl]-5'-yl)-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-1,1,1-trifluoromethanesulfonamide
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Used as a highly selective ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as palladium-catalyzed cross-couplings and enantioselective transformations. Its sterically demanding and electron-rich structure enhances catalytic efficiency and enantiocontrol. Commonly employed in the synthesis of chiral pharmaceuticals and fine chemicals where high enantiomeric excess is required. Also utilized in advanced materials research due to its rigid aromatic framework and sta

Used as a highly selective ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as palladium-catalyzed cross-couplings and enantioselective transformations. Its sterically demanding and electron-rich structure enhances catalytic efficiency and enantiocontrol. Commonly employed in the synthesis of chiral pharmaceuticals and fine chemicals where high enantiomeric excess is required. Also utilized in advanced materials research due to its rigid aromatic framework and stability under harsh reaction conditions.

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