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

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Reagent Code: #41039
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CAS Number 497172-36-8

science Other reagents with same CAS 497172-36-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 521.6100 g/mol
Formula C₃₅H₂₇N₃O₂
badge Registry Numbers
MDL Number MFCD32640763
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 such as hydrogenation, allylic alkylation, and cyclopropanation. Its rigid and well-defined structure, combined with the presence of chiral oxazoline rings, makes it highly effective in inducing enantioselectivity in the formation of chiral centers. It is often employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is crucial. Additionally, its ability to coordinate with various transition metals, such as palladium, rhodium, and iridium, enhances its versatility in catalytic applications. This compound is also explored in materials science for the development of chiral polymers and advanced molecular frameworks.

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inventory 50mg
10-20 days ฿2,268.00

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2,6-Bis((4R,5S)-4,5-diphenyl-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 such as hydrogenation, allylic alkylation, and cyclopropanation. Its rigid and well-defined structure, combined with the presence of chiral oxazoline rings, makes it highly effective in inducing enantioselectivity in the formation of chiral centers. It is often employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is crucial. Additionally, its abilit

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, allylic alkylation, and cyclopropanation. Its rigid and well-defined structure, combined with the presence of chiral oxazoline rings, makes it highly effective in inducing enantioselectivity in the formation of chiral centers. It is often employed in the synthesis of pharmaceuticals and fine chemicals where high enantiomeric purity is crucial. Additionally, its ability to coordinate with various transition metals, such as palladium, rhodium, and iridium, enhances its versatility in catalytic applications. This compound is also explored in materials science for the development of chiral polymers and advanced molecular frameworks.

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