(4R,4'R,5S,5'S)-2,2'-(Cyclobutane-1,1-diyl)bis(4,5-diphenyl-4,5-dihydrooxazole)

97%

Reagent Code: #229384
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CAS Number 2828431-95-2

science Other reagents with same CAS 2828431-95-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 498.61 g/mol
Formula C₃₄H₃₀N₂O₂
thermostat Physical Properties
Boiling Point 631.5±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.22±0.1 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cyclobutane core and oxazoline rings provide a well-defined chiral environment, making it effective in coordinating to metal centers such as copper or palladium. This complexation enables high stereoselectivity in reactions like cyclopropanations, Diels-Alder, and aldol reactions. Commonly employed in pharmaceutical synthesis where precise stereochemistry is critical. The ligand’s stability under various reaction conditions enhances its utility in both academic and industrial settings.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿14,300.00
inventory 250mg
10-20 days ฿24,280.00
(4R,4'R,5S,5'S)-2,2'-(Cyclobutane-1,1-diyl)bis(4,5-diphenyl-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cyclobutane core and oxazoline rings provide a well-defined chiral environment, making it effective in coordinating to metal centers such as copper or palladium. This complexation enables high stereoselectivity in reactions like cyclopropanations, Diels-Alder, and aldol reactions. Commonly employed in pharmaceutical synthesis where precise stereochemistry is critical. The ligand’s stabilit

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cyclobutane core and oxazoline rings provide a well-defined chiral environment, making it effective in coordinating to metal centers such as copper or palladium. This complexation enables high stereoselectivity in reactions like cyclopropanations, Diels-Alder, and aldol reactions. Commonly employed in pharmaceutical synthesis where precise stereochemistry is critical. The ligand’s stability under various reaction conditions enhances its utility in both academic and industrial settings.

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