(4R,5S)-4,5-Diphenyl-2-(pyridin-2-yl)-4,5-dihydrooxazole

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Reagent Code: #36978
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CAS Number 1108603-34-4

science Other reagents with same CAS 1108603-34-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.3500 g/mol
Formula C₂₀H₁₆N₂O
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in metal-catalyzed transformations, such as hydrogenation, to produce optically active compounds. Its rigid structure and ability to coordinate with metals make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is required. Its use extends to academic research for developing new catalytic methodologies and studying reaction mechanisms.

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inventory 100mg
10-20 days ฿3,879.00

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(4R,5S)-4,5-Diphenyl-2-(pyridin-2-yl)-4,5-dihydrooxazole
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in metal-catalyzed transformations, such as hydrogenation, to produce optically active compounds. Its rigid structure and ability to coordinate with metals make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where hig

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in metal-catalyzed transformations, such as hydrogenation, to produce optically active compounds. Its rigid structure and ability to coordinate with metals make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where high enantiomeric purity is required. Its use extends to academic research for developing new catalytic methodologies and studying reaction mechanisms.

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