1,1,1-trifluoro-N-[(11bS)-4-oxido-2,6-di-9-phenanthrenyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-Methanesulfonamide

98%

Reagent Code: #65715
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CAS Number 1256334-83-4

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 831.79 g/mol
Formula C₄₉H₂₉F₃NO₅PS
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in advanced organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure, featuring a phenanthrene-based dioxaphosphepin core, makes it highly effective in facilitating enantioselective transformations, which are crucial in the production of pharmaceuticals and fine chemicals. The trifluoromethanesulfonamide group enhances its stability and reactivity, allowing it to perform efficiently under various reaction conditions. Additionally, its application extends to material science, where it is explored for the development of chiral materials with potential uses in optoelectronics and nanotechnology.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿8,982.00
inventory 50mg
10-20 days ฿35,874.00

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1,1,1-trifluoro-N-[(11bS)-4-oxido-2,6-di-9-phenanthrenyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-Methanesulfonamide
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This compound is primarily utilized in advanced organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure, featuring a phenanthrene-based dioxaphosphepin core, makes it highly effective in facilitating enantioselective transformations, which are crucial in the production of pharmaceuticals and fine chemicals. The trifluoromethanesulfonamide group enhances its stability and reactivity, allowing it to perform efficiently under various reaction conditions.

This compound is primarily utilized in advanced organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure, featuring a phenanthrene-based dioxaphosphepin core, makes it highly effective in facilitating enantioselective transformations, which are crucial in the production of pharmaceuticals and fine chemicals. The trifluoromethanesulfonamide group enhances its stability and reactivity, allowing it to perform efficiently under various reaction conditions. Additionally, its application extends to material science, where it is explored for the development of chiral materials with potential uses in optoelectronics and nanotechnology.

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