(3aS,8aS)-4,4,8,8-Tetra([1,1':3',1''-terphenyl]-5'-yl)-2,2-dimethyltetrahydro-[1,3]dioxolo[4,5-e][1,3,2]dioxaphosphepine6-oxide

98%

Reagent Code: #237891
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CAS Number 2166542-09-0

science Other reagents with same CAS 2166542-09-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1121.3 g/mol
Formula C₇₉H₆₁O₅P
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a highly specialized ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions where precise stereochemical control is required. Its sterically bulky aryl groups and chiral dioxaphosphepine backbone make it effective in enantioselective transformations such as hydrogenations, C–C bond formations, and cycloadditions. Commonly employed in research and pharmaceutical synthesis to achieve high enantiomeric excess. Due to its complex structure, it is typically reserved for reactions where standard ligands fail to provide adequate selectivity or yield.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿1,200.00
(3aS,8aS)-4,4,8,8-Tetra([1,1':3',1''-terphenyl]-5'-yl)-2,2-dimethyltetrahydro-[1,3]dioxolo[4,5-e][1,3,2]dioxaphosphepine6-oxide
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Used as a highly specialized ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions where precise stereochemical control is required. Its sterically bulky aryl groups and chiral dioxaphosphepine backbone make it effective in enantioselective transformations such as hydrogenations, C–C bond formations, and cycloadditions. Commonly employed in research and pharmaceutical synthesis to achieve high enantiomeric excess. Due to its complex structure, it is typically reserved for r

Used as a highly specialized ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions where precise stereochemical control is required. Its sterically bulky aryl groups and chiral dioxaphosphepine backbone make it effective in enantioselective transformations such as hydrogenations, C–C bond formations, and cycloadditions. Commonly employed in research and pharmaceutical synthesis to achieve high enantiomeric excess. Due to its complex structure, it is typically reserved for reactions where standard ligands fail to provide adequate selectivity or yield.

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