2,6-Bis((4R,5R)-4,5-dihydro-4,5-diphenyl-2-oxazolyl)pyridine

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Reagent Code: #153316
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CAS Number 372200-56-1

science Other reagents with same CAS 372200-56-1

blur_circular Chemical Specifications

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Weight 521.6078 g/mol
Formula C₃₅H₂₇N₃O₂
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a tridentate chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as hydrogenation and transfer hydrogenation reactions. Its rigid pyridine core and oxazoline rings with defined stereochemistry enable high enantioselectivity when coordinated to transition metals like ruthenium, rhodium, or iridium. Commonly employed in the synthesis of chiral amines, alcohols, and pharmaceutical intermediates where control of stereochemistry is critical. Also utilized in research settings to develop new catalytic systems for asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,820.00
inventory 250mg
10-20 days ฿7,110.00
inventory 1g
10-20 days ฿28,410.00

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2,6-Bis((4R,5R)-4,5-dihydro-4,5-diphenyl-2-oxazolyl)pyridine
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Used as a tridentate chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as hydrogenation and transfer hydrogenation reactions. Its rigid pyridine core and oxazoline rings with defined stereochemistry enable high enantioselectivity when coordinated to transition metals like ruthenium, rhodium, or iridium. Commonly employed in the synthesis of chiral amines, alcohols, and pharmaceutical intermediates where control of stereochemistry is critical. Also utilized
Used as a tridentate chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations such as hydrogenation and transfer hydrogenation reactions. Its rigid pyridine core and oxazoline rings with defined stereochemistry enable high enantioselectivity when coordinated to transition metals like ruthenium, rhodium, or iridium. Commonly employed in the synthesis of chiral amines, alcohols, and pharmaceutical intermediates where control of stereochemistry is critical. Also utilized in research settings to develop new catalytic systems for asymmetric synthesis.
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