(R)-4-Benzyl-2-((R)-1-(diphenylphosphanyl)piperidin-2-yl)-4,5-dihydrooxazole

97%

Reagent Code: #229453
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CAS Number 2757084-65-2

science Other reagents with same CAS 2757084-65-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 428.51 g/mol
Formula C₂₇H₂₉N₂OP
thermostat Physical Properties
Boiling Point 563.8±60.0 °C(Predicted)
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 hydrogenation reactions. Its phosphine-oxazoline structure enables high stereocontrol, making it valuable in the synthesis of chiral pharmaceuticals and fine chemicals. Effective in rhodium- and iridium-catalyzed reactions, it helps produce single-enantiomer compounds important in drug development. The rigid piperidine backbone and bulky diphenylphosphino group enhance catalyst stability and selectivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,190.00
inventory 250mg
10-20 days ฿18,940.00

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(R)-4-Benzyl-2-((R)-1-(diphenylphosphanyl)piperidin-2-yl)-4,5-dihydrooxazole
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation reactions. Its phosphine-oxazoline structure enables high stereocontrol, making it valuable in the synthesis of chiral pharmaceuticals and fine chemicals. Effective in rhodium- and iridium-catalyzed reactions, it helps produce single-enantiomer compounds important in drug development. The rigid piperidine backbone and bulky diphenylphosphino group enhance catalyst stability and selectivity.

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective hydrogenation reactions. Its phosphine-oxazoline structure enables high stereocontrol, making it valuable in the synthesis of chiral pharmaceuticals and fine chemicals. Effective in rhodium- and iridium-catalyzed reactions, it helps produce single-enantiomer compounds important in drug development. The rigid piperidine backbone and bulky diphenylphosphino group enhance catalyst stability and selectivity.

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