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

≥98%,99%e.e.

Reagent Code: #70601
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CAS Number 365215-38-9

science Other reagents with same CAS 365215-38-9

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 compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis. It serves as a chiral ligand in transition metal-catalyzed reactions, enabling the production of optically active compounds. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where precise stereochemistry is crucial for efficacy and safety. Additionally, it is employed in organic synthesis to facilitate complex transformations, such as carbon-carbon bond formations, with high enantioselectivity. Its robust structure and ability to coordinate with various metals make it a versatile tool in advanced chemical research and industrial processes.

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Test Parameter Specification
Appearance White to light-yellow to light-brown or gray powder or crystals
Purity 98-100
Infrared Spectrum Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,080.00
inventory 500mg
10-20 days ฿1,760.00
inventory 100mg
10-20 days ฿520.00

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2,6-Bis[(4R)-benzyl-2-oxazolin-2-yl]pyridine
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This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis. It serves as a chiral ligand in transition metal-catalyzed reactions, enabling the production of optically active compounds. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where precise stereochemistry is crucial for efficacy and safety. Additionally, it is employed in organic synthesis to facilitate complex transformations, such as carbon-carbon bond

This compound is primarily utilized in asymmetric catalysis, particularly in enantioselective synthesis. It serves as a chiral ligand in transition metal-catalyzed reactions, enabling the production of optically active compounds. Its application is significant in the pharmaceutical industry for the synthesis of chiral drugs, where precise stereochemistry is crucial for efficacy and safety. Additionally, it is employed in organic synthesis to facilitate complex transformations, such as carbon-carbon bond formations, with high enantioselectivity. Its robust structure and ability to coordinate with various metals make it a versatile tool in advanced chemical research and industrial processes.

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