2,6-Bis((R)-4-ethyl-4,5-dihydrooxazol-2-yl)pyridine

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Reagent Code: #41041
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CAS Number 131864-68-1

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Weight 273.3303 g/mol
Formula C₁₅H₁₉N₃O₂
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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 transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. This ligand is also applied in the synthesis of pharmaceuticals and fine chemicals, where achieving specific enantiomers is essential for biological activity or desired properties. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring chiral induction mechanisms.

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inventory 100mg
10-20 days ฿963.00

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2,6-Bis((R)-4-ethyl-4,5-dihydrooxazol-2-yl)pyridine
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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 transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. This ligand is also applied in the synthesis of pharmaceuticals and fine chemicals, where achieving

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 transition metal-catalyzed processes, such as hydrogenation, to produce chiral molecules with high optical purity. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. This ligand is also applied in the synthesis of pharmaceuticals and fine chemicals, where achieving specific enantiomers is essential for biological activity or desired properties. Additionally, it finds use in academic research for developing new catalytic methodologies and exploring chiral induction mechanisms.

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