(11bS)-2,6-bis(3,5-di-tert-butylphenyl)-4-hydroxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

98%

Reagent Code: #236599
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CAS Number 1442645-05-7

science Other reagents with same CAS 1442645-05-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 724.91 g/mol
Formula C₄₈H₅₃O₄P
badge Registry Numbers
MDL Number MFCD28139326
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and C–C bond formation. Its sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in rhodium- and ruthenium-based catalytic systems for producing high enantiomeric excess. Also employed in academic and industrial research for developing enantioselective transformations.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,050.00
inventory 250mg
10-20 days ฿11,700.00
inventory 1g
10-20 days ฿37,210.00
inventory 100mg
10-20 days ฿6,040.00

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(11bS)-2,6-bis(3,5-di-tert-butylphenyl)-4-hydroxydinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and C–C bond formation. Its sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in rhodium- and ruthenium-based catalytic systems for producing high enantiomeric excess. Also employed in academic and industrial research for developing enantioselective transformatio

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and C–C bond formation. Its sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in rhodium- and ruthenium-based catalytic systems for producing high enantiomeric excess. Also employed in academic and industrial research for developing enantioselective transformations.

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