(S)-4-(tert-Butyl)-2-(2-(2-(diphenylphosphino)phenyl)propan-2-yl)-4,5-dihydrooxazole

97%

Reagent Code: #237616
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CAS Number 947618-07-7

science Other reagents with same CAS 947618-07-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 429.53 g/mol
Formula C₂₈H₃₂NOP
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 transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its phosphine-oxazoline structure provides excellent stereocontrol, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. The tert-butyl and diphenylphosphino groups enhance steric bulk and electron density, improving catalytic activity and selectivity. Commonly employed with palladium, rhodium, or iridium complexes in homogeneous catalysis.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,480.00
inventory 100mg
10-20 days ฿11,200.00
inventory 250mg
10-20 days ฿16,800.00
inventory 1g
10-20 days ฿51,520.00

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(S)-4-(tert-Butyl)-2-(2-(2-(diphenylphosphino)phenyl)propan-2-yl)-4,5-dihydrooxazole
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its phosphine-oxazoline structure provides excellent stereocontrol, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. The tert-butyl and diphenylphosphino groups enhance steric bulk and electron density, improving catalytic activity and selectivity. Commonly employed with palladium, rhodium, or iridium complexes in h

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as hydrogenation and cross-coupling. Its phosphine-oxazoline structure provides excellent stereocontrol, making it valuable in the synthesis of enantiomerically pure pharmaceuticals and fine chemicals. The tert-butyl and diphenylphosphino groups enhance steric bulk and electron density, improving catalytic activity and selectivity. Commonly employed with palladium, rhodium, or iridium complexes in homogeneous catalysis.

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