(4S,4'S)-2,2'-(Oxybis(2,1-phenylene))bis(4-phenyl-4,5-dihydrooxazole)

98%

Reagent Code: #237414
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CAS Number 1613706-51-6

science Other reagents with same CAS 1613706-51-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 460.52 g/mol
Formula C₃₀H₂₄N₂O₃
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline-phenyl architecture enables high stereocontrol in metal-catalyzed reactions such as cyclopropanations, Diels-Alder, and aldol reactions. Commonly coordinates with copper, palladium, or rhodium to form active catalytic species. Valued for promoting high enantiomeric excess in synthesis of pharmaceuticals and fine chemicals. Also applied in the development of chiral sensors and materials requiring precise spatial arrangement.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,340.00
inventory 250mg
10-20 days ฿15,870.00
inventory 1g
10-20 days ฿45,070.00

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(4S,4'S)-2,2'-(Oxybis(2,1-phenylene))bis(4-phenyl-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline-phenyl architecture enables high stereocontrol in metal-catalyzed reactions such as cyclopropanations, Diels-Alder, and aldol reactions. Commonly coordinates with copper, palladium, or rhodium to form active catalytic species. Valued for promoting high enantiomeric excess in synthesis of pharmaceuticals and fine chemicals. Also applied in the development of chiral sensors and mat

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid oxazoline-phenyl architecture enables high stereocontrol in metal-catalyzed reactions such as cyclopropanations, Diels-Alder, and aldol reactions. Commonly coordinates with copper, palladium, or rhodium to form active catalytic species. Valued for promoting high enantiomeric excess in synthesis of pharmaceuticals and fine chemicals. Also applied in the development of chiral sensors and materials requiring precise spatial arrangement.

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