(S)-2,2'-Bis[di(3,5-dimethoxyphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl

98%

Reagent Code: #233223
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CAS Number 1448723-00-9

science Other reagents with same CAS 1448723-00-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 822.83 g/mol
Formula C₄₆H₄₈O₁₀P₂
thermostat Physical Properties
Boiling Point 863.3±65.0 °C(Predicted)
inventory_2 Storage & Handling
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It is highly effective in enantioselective transformations such as hydrogenation, cross-coupling, and C–H activation, where it helps achieve high enantiomeric excess. Its sterically hindered and electron-rich structure enhances catalyst stability and selectivity. Commonly employed with rhodium, ruthenium, or palladium complexes in pharmaceutical synthesis and fine chemical production to control stereochemistry in complex molecule assembly.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿11,140.00
250mg
10-20 days ฿16,720.00
(S)-2,2'-Bis[di(3,5-dimethoxyphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl
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Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It is highly effective in enantioselective transformations such as hydrogenation, cross-coupling, and C–H activation, where it helps achieve high enantiomeric excess. Its sterically hindered and electron-rich structure enhances catalyst stability and selectivity. Commonly employed with rhodium, ruthenium, or palladium complexes in pharmaceutical synthesis and fine chemical production to control stereoch

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions. It is highly effective in enantioselective transformations such as hydrogenation, cross-coupling, and C–H activation, where it helps achieve high enantiomeric excess. Its sterically hindered and electron-rich structure enhances catalyst stability and selectivity. Commonly employed with rhodium, ruthenium, or palladium complexes in pharmaceutical synthesis and fine chemical production to control stereochemistry in complex molecule assembly.

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