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

98%

Reagent Code: #215963
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CAS Number 1486486-92-3

science Other reagents with same CAS 1486486-92-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 691.61 g/mol
Formula C₃₅H₂₅F₃NO₇PS
thermostat Physical Properties
Boiling Point 802.0±75.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.52±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 C–C bond-forming reactions. Its rigid dinaphthyl backbone and phosphorus center with tunable electronic properties make it effective in promoting high enantioselectivity in metal-catalyzed reactions. Commonly employed in palladium- or rhodium-catalyzed asymmetric allylic substitutions and cross-coupling reactions, especially in the pharmaceutical industry for synthesizing optically active intermediates. The trifluoromethanesulfonamide group enhances stability and influences coordination behavior with metals, improving catalytic efficiency and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,540.00
inventory 100mg
10-20 days ฿9,420.00
inventory 250mg
10-20 days ฿16,000.00
N-((11bR)-2,6-Bis(4-methoxyphenyl)-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 C–C bond-forming reactions. Its rigid dinaphthyl backbone and phosphorus center with tunable electronic properties make it effective in promoting high enantioselectivity in metal-catalyzed reactions. Commonly employed in palladium- or rhodium-catalyzed asymmetric allylic substitutions and cross-coupling reactions, especially in the pharmaceutical industry for synthesizing optically active in

Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as C–C bond-forming reactions. Its rigid dinaphthyl backbone and phosphorus center with tunable electronic properties make it effective in promoting high enantioselectivity in metal-catalyzed reactions. Commonly employed in palladium- or rhodium-catalyzed asymmetric allylic substitutions and cross-coupling reactions, especially in the pharmaceutical industry for synthesizing optically active intermediates. The trifluoromethanesulfonamide group enhances stability and influences coordination behavior with metals, improving catalytic efficiency and selectivity.

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