(4R,4'R)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-phenyl-4,5-dihydrooxazole)

97%

Reagent Code: #231321
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CAS Number 2247206-06-8

science Other reagents with same CAS 2247206-06-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 598.820 g/mol
Formula C₄₁H₄₆N₂O₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as cyclopropanation, Diels-Alder, and aldol reactions. Its rigid bisoxazoline structure coordinates with metal centers like copper(II) or iron(II), forming highly selective catalysts that induce chirality in the product. Widely applied in pharmaceutical synthesis where control of stereochemistry is critical. The bulky tert-butyl groups enhance steric differentiation, improving enantioselectivity. Also employed in the development of chiral sensors and materials for enantiomeric separation.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,900.00
inventory 250mg
10-20 days ฿10,380.00
inventory 1g
10-20 days ฿27,990.00
(4R,4'R)-2,2'-(1,3-Bis(4-(tert-butyl)phenyl)propane-2,2-diyl)bis(4-phenyl-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as cyclopropanation, Diels-Alder, and aldol reactions. Its rigid bisoxazoline structure coordinates with metal centers like copper(II) or iron(II), forming highly selective catalysts that induce chirality in the product. Widely applied in pharmaceutical synthesis where control of stereochemistry is critical. The bulky tert-butyl groups enhance steric differentiation, improving enantioselectivity

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as cyclopropanation, Diels-Alder, and aldol reactions. Its rigid bisoxazoline structure coordinates with metal centers like copper(II) or iron(II), forming highly selective catalysts that induce chirality in the product. Widely applied in pharmaceutical synthesis where control of stereochemistry is critical. The bulky tert-butyl groups enhance steric differentiation, improving enantioselectivity. Also employed in the development of chiral sensors and materials for enantiomeric separation.

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