N-[(11bS)-2,6-Bis[4-(1,1-dimethylethyl)phenyl]-8,9,10,11,12,13,14,15-octahydro-4-oxidodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl]-1,1,1-trifluoromethanesulfonamide

98%

Reagent Code: #220510
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CAS Number 2757287-29-7

science Other reagents with same CAS 2757287-29-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 751.83 g/mol
Formula C₄₁H₄₅F₃NO₅PS
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its sterically hindered structure and electron-donating properties enhance selectivity and reactivity with transition metals like palladium, rhodium, and iridium. Commonly applied in pharmaceutical and fine chemical industries to produce single-enantiomer compounds. Exhibits high stability under various reaction conditions, making it suitable for industrial-scale processes requiring precise stereochemical control.

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inventory 100mg
10-20 days ฿7,150.00

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N-[(11bS)-2,6-Bis[4-(1,1-dimethylethyl)phenyl]-8,9,10,11,12,13,14,15-octahydro-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 hydrogenation and cross-coupling reactions. Its sterically hindered structure and electron-donating properties enhance selectivity and reactivity with transition metals like palladium, rhodium, and iridium. Commonly applied in pharmaceutical and fine chemical industries to produce single-enantiomer compounds. Exhibits high stability under various reaction conditions, making it suitable for i

Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective transformations such as hydrogenation and cross-coupling reactions. Its sterically hindered structure and electron-donating properties enhance selectivity and reactivity with transition metals like palladium, rhodium, and iridium. Commonly applied in pharmaceutical and fine chemical industries to produce single-enantiomer compounds. Exhibits high stability under various reaction conditions, making it suitable for industrial-scale processes requiring precise stereochemical control.

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