(4R,5S)-2-(1,10-Phenanthrolin-2-yl)-4,5-diphenyl-4,5-dihydrooxazole

98%

Reagent Code: #229459
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CAS Number 2828438-21-5

science Other reagents with same CAS 2828438-21-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 401.46 g/mol
Formula C₂₇H₁₉N₃O
thermostat Physical Properties
Boiling Point 628.0±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.26±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid structure and ability to coordinate with transition metals like copper or palladium make it effective in promoting stereoselective reactions such as cyclopropanations, aldol additions, and allylic alkylations. The oxazole and phenanthroline moieties enhance metal binding and influence stereochemical outcomes, leading to high enantiomeric excess in the synthesized products. Commonly applied in pharmaceutical and fine chemical synthesis where precise stereochemistry is critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,720.00
inventory 250mg
10-20 days ฿19,060.00
inventory 1g
10-20 days ฿55,060.00

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(4R,5S)-2-(1,10-Phenanthrolin-2-yl)-4,5-diphenyl-4,5-dihydrooxazole
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid structure and ability to coordinate with transition metals like copper or palladium make it effective in promoting stereoselective reactions such as cyclopropanations, aldol additions, and allylic alkylations. The oxazole and phenanthroline moieties enhance metal binding and influence stereochemical outcomes, leading to high enantiomeric excess in the synthesized products. Commonly applied

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid structure and ability to coordinate with transition metals like copper or palladium make it effective in promoting stereoselective reactions such as cyclopropanations, aldol additions, and allylic alkylations. The oxazole and phenanthroline moieties enhance metal binding and influence stereochemical outcomes, leading to high enantiomeric excess in the synthesized products. Commonly applied in pharmaceutical and fine chemical synthesis where precise stereochemistry is critical.

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