(4S,5S)-2-(1,8-Naphthyridin-2-yl)-4,5-diphenyl-4,5-dihydrooxazole

98%

Reagent Code: #237474
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CAS Number 2757082-53-2

science Other reagents with same CAS 2757082-53-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 351.4 g/mol
Formula C₂₃H₁₇N₃O
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used in organic synthesis as a chiral auxiliary and ligand in asymmetric catalysis. Its rigid oxazole framework and naphthyridine moiety make it effective in promoting enantioselective reactions, particularly in the formation of carbon-carbon bonds. Commonly employed in transition metal-catalyzed reactions such as asymmetric hydrogenation and cycloadditions, where it helps achieve high enantiomeric excess. Also investigated for its potential in luminescent materials due to the extended aromatic system, showing promise in optoelectronic applications and sensor development.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,490.00
inventory 1g
10-20 days ฿31,470.00
(4S,5S)-2-(1,8-Naphthyridin-2-yl)-4,5-diphenyl-4,5-dihydrooxazole
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Used in organic synthesis as a chiral auxiliary and ligand in asymmetric catalysis. Its rigid oxazole framework and naphthyridine moiety make it effective in promoting enantioselective reactions, particularly in the formation of carbon-carbon bonds. Commonly employed in transition metal-catalyzed reactions such as asymmetric hydrogenation and cycloadditions, where it helps achieve high enantiomeric excess. Also investigated for its potential in luminescent materials due to the extended aromatic system, s

Used in organic synthesis as a chiral auxiliary and ligand in asymmetric catalysis. Its rigid oxazole framework and naphthyridine moiety make it effective in promoting enantioselective reactions, particularly in the formation of carbon-carbon bonds. Commonly employed in transition metal-catalyzed reactions such as asymmetric hydrogenation and cycloadditions, where it helps achieve high enantiomeric excess. Also investigated for its potential in luminescent materials due to the extended aromatic system, showing promise in optoelectronic applications and sensor development.

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