N-((11BS)-2,6-di(naphthalen-2-yl)-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)-1,1,1-trifluoromethanesulfonamide

97%

Reagent Code: #219821
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CAS Number 2757287-37-7

science Other reagents with same CAS 2757287-37-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 731.67 g/mol
Formula C₄₁H₂₅F₃NO₅PS
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a highly effective chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as allylic substitutions and cross-coupling reactions. Its rigid, sterically hindered structure enhances stereocontrol, making it valuable in pharmaceutical and fine chemical manufacturing where high enantiomeric purity is required. The presence of trifluoromethanesulfonamide improves stability and electronic tuning, contributing to superior catalytic performance under mild reaction conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿3,610.00
100mg
10-20 days ฿4,480.00
250mg
10-20 days ฿10,360.00
1g
10-20 days ฿35,020.00

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N-((11BS)-2,6-di(naphthalen-2-yl)-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 highly effective chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as allylic substitutions and cross-coupling reactions. Its rigid, sterically hindered structure enhances stereocontrol, making it valuable in pharmaceutical and fine chemical manufacturing where high enantiomeric purity is required. The presence of trifluoromethanesulfonamide improves stability and electronic tuning, contributing to superior catalytic performance under mild reacti
Used as a highly effective chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as allylic substitutions and cross-coupling reactions. Its rigid, sterically hindered structure enhances stereocontrol, making it valuable in pharmaceutical and fine chemical manufacturing where high enantiomeric purity is required. The presence of trifluoromethanesulfonamide improves stability and electronic tuning, contributing to superior catalytic performance under mild reaction conditions.
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