(S)-4-(tert-Butyl)-2-(1,10-phenanthrolin-2-yl)-4,5-dihydrooxazole

98%

Reagent Code: #233455
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CAS Number 2828438-14-6

science Other reagents with same CAS 2828438-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 305.38 g/mol
Formula C₁₉H₁₉N₃O
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective oxidation and cyclization reactions. Its rigid phenanthroline backbone and oxazoline ring enhance stereocontrol, making it valuable in pharmaceutical and fine chemical manufacturing where high enantiomeric purity is required. Effective in copper-catalyzed reactions, it helps form carbon–oxygen and carbon–nitrogen bonds with high selectivity. Also applied in the development of new catalytic systems for sustainable chemistry due to its stability and reusability under various reaction conditions.

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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

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(S)-4-(tert-Butyl)-2-(1,10-phenanthrolin-2-yl)-4,5-dihydrooxazole
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Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective oxidation and cyclization reactions. Its rigid phenanthroline backbone and oxazoline ring enhance stereocontrol, making it valuable in pharmaceutical and fine chemical manufacturing where high enantiomeric purity is required. Effective in copper-catalyzed reactions, it helps form carbon–oxygen and carbon–nitrogen bonds with high selectivity. Also applied in the development of new catalytic systems for sustainable c

Used as a chiral catalyst ligand in asymmetric synthesis, particularly in enantioselective oxidation and cyclization reactions. Its rigid phenanthroline backbone and oxazoline ring enhance stereocontrol, making it valuable in pharmaceutical and fine chemical manufacturing where high enantiomeric purity is required. Effective in copper-catalyzed reactions, it helps form carbon–oxygen and carbon–nitrogen bonds with high selectivity. Also applied in the development of new catalytic systems for sustainable chemistry due to its stability and reusability under various reaction conditions.

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