N-​[(11bS)​-​2,​6-​Bis[3,​5-​bis(trifluoromethyl)​phenyl]​-​8,​9,​10,​11,​12,​13,​14,​15-​octahydro-​4-​oxido-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]​-​1,​1,​1-​trifluoromethanesulfonamide

≥98%,≥99%e.e.

Reagent Code: #57515

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 911.6 g/mol
Formula C₃₇H₂₅F₁₅NO₅PS
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a crucial role in facilitating reactions where the formation of a specific enantiomer is desired, such as in the production of pharmaceuticals or fine chemicals. Its unique structure, featuring trifluoromethyl groups and a dioxaphosphepin core, enhances its ability to induce high enantioselectivity and reactivity in various catalytic processes. Additionally, it is employed in the development of advanced materials and as a key component in research focused on understanding chiral induction mechanisms.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿35,964.00

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N-​[(11bS)​-​2,​6-​Bis[3,​5-​bis(trifluoromethyl)​phenyl]​-​8,​9,​10,​11,​12,​13,​14,​15-​octahydro-​4-​oxido-dinaphtho[2,​1-​d:1',​2'-​f]​[1,​3,​2]​dioxaphosphepin-​4-​yl]​-​1,​1,​1-​trifluoromethanesulfonamide
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a crucial role in facilitating reactions where the formation of a specific enantiomer is desired, such as in the production of pharmaceuticals or fine chemicals. Its unique structure, featuring trifluoromethyl groups and a dioxaphosphepin core, enhances its ability to induce high enantioselectivity and reactivity in various catalytic processes. Additionally, it is employed

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a crucial role in facilitating reactions where the formation of a specific enantiomer is desired, such as in the production of pharmaceuticals or fine chemicals. Its unique structure, featuring trifluoromethyl groups and a dioxaphosphepin core, enhances its ability to induce high enantioselectivity and reactivity in various catalytic processes. Additionally, it is employed in the development of advanced materials and as a key component in research focused on understanding chiral induction mechanisms.

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