2,6-Bis[(4S)-benzyl-2-oxazolin-2-yl]pyridine

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Reagent Code: #70605
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CAS Number 151670-69-8

science Other reagents with same CAS 151670-69-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 397.5 g/mol
Formula C₂₅H₂₃N₃O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cyclopropanation. Its unique structure allows it to coordinate with transition metals, forming complexes that enhance the stereochemical control of reactions. This makes it valuable in the production of pharmaceuticals, where achieving specific enantiomers is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of fine chemicals and advanced materials, where precise stereochemistry is required. Its application extends to academic research, where it serves as a tool for developing new catalytic methodologies.

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Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿3,530.00
inventory 100mg
10-20 days ฿750.00

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2,6-Bis[(4S)-benzyl-2-oxazolin-2-yl]pyridine
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cyclopropanation. Its unique structure allows it to coordinate with transition metals, forming complexes that enhance the stereochemical control of reactions. This makes it valuable in the production of pharmaceuticals, where achieving specific enantiomers is crucial for

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, allylic alkylation, and cyclopropanation. Its unique structure allows it to coordinate with transition metals, forming complexes that enhance the stereochemical control of reactions. This makes it valuable in the production of pharmaceuticals, where achieving specific enantiomers is crucial for drug efficacy and safety. Additionally, it is employed in the synthesis of fine chemicals and advanced materials, where precise stereochemistry is required. Its application extends to academic research, where it serves as a tool for developing new catalytic methodologies.

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