4,6-Bis((R)-4-(tert-butyl)-4,5-dihydrooxazol-2-yl)dibenzo[b,d]furan

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Reagent Code: #153238
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CAS Number 2757082-90-7

science Other reagents with same CAS 2757082-90-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 418.53 g/mol
Formula C₂₆H₃₀N₂O₃
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereoselectivity in transformations such as hydrogenation, C–C bond formation, and cycloadditions. Its rigid dibenzofuran backbone and oxazoline moieties enhance metal coordination and stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with metals like palladium, rhodium, or iridium to achieve efficient chiral induction in industrial and academic research settings.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,950.00
inventory 250mg
10-20 days ฿10,390.00
inventory 1g
10-20 days ฿29,260.00

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4,6-Bis((R)-4-(tert-butyl)-4,5-dihydrooxazol-2-yl)dibenzo[b,d]furan
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereoselectivity in transformations such as hydrogenation, C–C bond formation, and cycloadditions. Its rigid dibenzofuran backbone and oxazoline moieties enhance metal coordination and stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with metals like palladium, rhodium, or

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective transition metal-catalyzed reactions. It plays a key role in promoting high stereoselectivity in transformations such as hydrogenation, C–C bond formation, and cycloadditions. Its rigid dibenzofuran backbone and oxazoline moieties enhance metal coordination and stereocontrol, making it valuable in the synthesis of optically active pharmaceuticals and fine chemicals. Commonly employed with metals like palladium, rhodium, or iridium to achieve efficient chiral induction in industrial and academic research settings.

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