(S)-4-Cyclohexyl-2-(2-(diphenylphosphanyl)phenyl)-4,5-dihydrooxazole

98%

Reagent Code: #236897
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CAS Number 2634687-58-2

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 413.4911 g/mol
Formula C₂₇H₂₈NOP
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its phosphine-oxazoline structure provides excellent stereocontrol, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. The rigid cyclohexyl group enhances stereoselectivity by restricting conformational flexibility. Commonly employed with palladium, rhodium, or iridium complexes to achieve high enantioselectivity in C–C and C–H bond formation processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,130.00
inventory 250mg
10-20 days ฿11,500.00
inventory 1g
10-20 days ฿43,060.00
(S)-4-Cyclohexyl-2-(2-(diphenylphosphanyl)phenyl)-4,5-dihydrooxazole
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its phosphine-oxazoline structure provides excellent stereocontrol, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. The rigid cyclohexyl group enhances stereoselectivity by restricting conformational flexibility. Commonly employed with palladium, rhodium, or iridium complexes to achieve high en

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling reactions. Its phosphine-oxazoline structure provides excellent stereocontrol, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. The rigid cyclohexyl group enhances stereoselectivity by restricting conformational flexibility. Commonly employed with palladium, rhodium, or iridium complexes to achieve high enantioselectivity in C–C and C–H bond formation processes.

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