(1S,1'S,2R,2'R)-2,2'-Di-tert-butyl-2,2',3,3'-tetrahydro-1H,1'H-1,1'-biiSophosphindole

97%

Reagent Code: #233164
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CAS Number 795290-34-5

science Other reagents with same CAS 795290-34-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 382.46 g/mol
Formula C₂₄H₃₂P₂
badge Registry Numbers
MDL Number MFCD11045432
thermostat Physical Properties
Melting Point 215-226 °C
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, cross-coupling, and C–H activation. Its rigid, sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in palladium- and rhodium-based catalytic systems where high stereocontrol is required. Also employed in the development of novel catalysts for industrial-scale enantioselective transformations.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿14,850.00
inventory 100mg
10-20 days ฿40,700.00

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(1S,1'S,2R,2'R)-2,2'-Di-tert-butyl-2,2',3,3'-tetrahydro-1H,1'H-1,1'-biiSophosphindole
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, cross-coupling, and C–H activation. Its rigid, sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in palladium- and rhodium-based catalytic systems where high stereocontrol is required. Also employed in the development of novel catalysts for industrial-scale enantioselectiv

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation, cross-coupling, and C–H activation. Its rigid, sterically hindered structure enhances enantioselectivity, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Effective in palladium- and rhodium-based catalytic systems where high stereocontrol is required. Also employed in the development of novel catalysts for industrial-scale enantioselective transformations.

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