1,​1,​1-Trifluoro-​N-​[(11bR)​-​4-​oxido-​2,​6-​diphenyldinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]methanesulfonamide

≥98%,≥99% e.e.

Reagent Code: #70540
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CAS Number 1010799-98-0

science Other reagents with same CAS 1010799-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 631.6 g/mol
Formula C₃₃H₂₁F₃NO₅PS
thermostat Physical Properties
Boiling Point 761.1±70.0 °C
inventory_2 Storage & Handling
Density 1.54±0.1 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure, featuring a trifluoromethyl group and a dioxaphosphepin ring system, makes it highly effective in inducing enantioselectivity. It is often employed in the synthesis of complex molecules, such as pharmaceuticals, where controlling the stereochemistry is crucial. Additionally, its sulfonamide moiety enhances its stability and reactivity, making it suitable for use in demanding chemical environments. The compound is particularly valued in the production of optically active intermediates, which are essential in the development of drugs and fine chemicals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,770.00

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1,​1,​1-Trifluoro-​N-​[(11bR)​-​4-​oxido-​2,​6-​diphenyldinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]methanesulfonamide
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This compound is primarily utilized in the field of organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure, featuring a trifluoromethyl group and a dioxaphosphepin ring system, makes it highly effective in inducing enantioselectivity. It is often employed in the synthesis of complex molecules, such as pharmaceuticals, where controlling the stereochemistry is crucial. Additionally, its sulfonamide moiety enhances its stability and reactivity, making it

This compound is primarily utilized in the field of organic synthesis, particularly as a chiral catalyst or ligand in asymmetric reactions. Its unique structure, featuring a trifluoromethyl group and a dioxaphosphepin ring system, makes it highly effective in inducing enantioselectivity. It is often employed in the synthesis of complex molecules, such as pharmaceuticals, where controlling the stereochemistry is crucial. Additionally, its sulfonamide moiety enhances its stability and reactivity, making it suitable for use in demanding chemical environments. The compound is particularly valued in the production of optically active intermediates, which are essential in the development of drugs and fine chemicals.

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