2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine

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Reagent Code: #153339
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CAS Number 410092-98-7

science Other reagents with same CAS 410092-98-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 521.62 g/mol
Formula C₃₅H₂₇N₃O₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations. It forms stable complexes with transition metals such as rhodium, ruthenium, and iridium, which are employed in hydrogenation reactions of prochiral substrates like ketones, alkenes, and imines. The rigid pyridine backbone and chiral oxazoline rings provide excellent stereocontrol, leading to high enantiomeric excess in the products. It is particularly effective in industrial synthesis of pharmaceuticals and fine chemicals where precise chirality is required. Its robustness under various reaction conditions and ease of recovery make it a preferred choice in both academic and industrial settings.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,620.00
inventory 100mg
10-20 days ฿3,160.00
inventory 250mg
10-20 days ฿7,880.00
inventory 1g
10-20 days ฿27,380.00

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2,6-Bis((4S,5S)-4,5-diphenyl-4,5-dihydrooxazol-2-yl)pyridine
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Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations. It forms stable complexes with transition metals such as rhodium, ruthenium, and iridium, which are employed in hydrogenation reactions of prochiral substrates like ketones, alkenes, and imines. The rigid pyridine backbone and chiral oxazoline rings provide excellent stereocontrol, leading to high enantiomeric excess in the products. It is particularly effective in industrial synthe

Widely used as a chiral ligand in asymmetric catalysis, this compound plays a key role in enantioselective transformations. It forms stable complexes with transition metals such as rhodium, ruthenium, and iridium, which are employed in hydrogenation reactions of prochiral substrates like ketones, alkenes, and imines. The rigid pyridine backbone and chiral oxazoline rings provide excellent stereocontrol, leading to high enantiomeric excess in the products. It is particularly effective in industrial synthesis of pharmaceuticals and fine chemicals where precise chirality is required. Its robustness under various reaction conditions and ease of recovery make it a preferred choice in both academic and industrial settings.

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