(11bR)-N-(2,6-bis(4-nitrophenyl)-4-oxido-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-1,1,1-trifluoromethanesulfonamide

97%

Reagent Code: #229253
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CAS Number 2758008-05-6

science Other reagents with same CAS 2758008-05-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 729.61 g/mol
Formula C₃₃H₂₇F₃N₃O₉PS
thermostat Physical Properties
Boiling Point 840.3±75.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.60±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 rigid dinaphthyl backbone and phosphorus center with defined stereochemistry enable high enantioselectivity in the production of pharmaceutical intermediates and fine chemicals. The presence of electron-withdrawing nitro groups enhances ligand stability and influences metal coordination, improving catalytic efficiency. Commonly employed with transition metals like palladium, rhodium, or iridium in homogeneous catalysis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,400.00
inventory 250mg
10-20 days ฿23,050.00

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(11bR)-N-(2,6-bis(4-nitrophenyl)-4-oxido-8,9,10,11,12,13,14,15-octahydrodinaphtho[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 rigid dinaphthyl backbone and phosphorus center with defined stereochemistry enable high enantioselectivity in the production of pharmaceutical intermediates and fine chemicals. The presence of electron-withdrawing nitro groups enhances ligand stability and influences metal coordination, improving catalytic efficiency. Commonly employed with tr

Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its rigid dinaphthyl backbone and phosphorus center with defined stereochemistry enable high enantioselectivity in the production of pharmaceutical intermediates and fine chemicals. The presence of electron-withdrawing nitro groups enhances ligand stability and influences metal coordination, improving catalytic efficiency. Commonly employed with transition metals like palladium, rhodium, or iridium in homogeneous catalysis.

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