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

98%

Reagent Code: #215782
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CAS Number 2757287-63-9

science Other reagents with same CAS 2757287-63-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 687.67 g/mol
Formula C₃₇H₂₉F₃NO₅PS
thermostat Physical Properties
Boiling Point 769.2±70.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.45±0.1 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its sterically hindered, electron-rich structure enhances selectivity and reactivity with transition metals like palladium, rhodium, and iridium. Widely applied in pharmaceutical and fine chemical industries to produce single-enantiomer compounds, where high optical purity is critical. The trifluoromethanesulfonamide group improves stability and coordination ability, making it effective under demanding reaction conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿12,840.00
100mg
10-20 days ฿19,250.00
(11bR)-N-(2,6-Bis(3,5-dimethylphenyl)-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 chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its sterically hindered, electron-rich structure enhances selectivity and reactivity with transition metals like palladium, rhodium, and iridium. Widely applied in pharmaceutical and fine chemical industries to produce single-enantiomer compounds, where high optical purity is critical. The trifluoromethanesulfonamide group improves stability and co

Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its sterically hindered, electron-rich structure enhances selectivity and reactivity with transition metals like palladium, rhodium, and iridium. Widely applied in pharmaceutical and fine chemical industries to produce single-enantiomer compounds, where high optical purity is critical. The trifluoromethanesulfonamide group improves stability and coordination ability, making it effective under demanding reaction conditions.

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