2,6-Bis[4R-4-phenyl-2-oxazolinyl]pyridine

98%

Reagent Code: #69831
label
Alias (R,R)-2,6-bis(4-phenyl-2-oxazolin-2-yl)pyridine
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CAS Number 128249-70-7

science Other reagents with same CAS 128249-70-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 369.42 g/mol
Formula C₂₃H₁₉N₃O₂
badge Registry Numbers
MDL Number MFCD01863585
thermostat Physical Properties
Melting Point 171-175 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8 °C

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a critical role in facilitating reactions such as hydrogenation, allylic alkylation, and Diels-Alder reactions, where it helps produce chiral compounds with high enantiomeric purity. Its application is significant in the pharmaceutical industry for synthesizing enantiomerically pure drugs. Additionally, it is utilized in organic chemistry research for developing novel catalytic processes and studying stereoselective transformations. Its rigid structure and ability to coordinate with metals make it a valuable tool in creating efficient and selective catalysts.

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Test Parameter Specification
Melting point 171-175
Purity (HPLC) 98-100
Purity (Nonaqueous Titration) 97.5-102.5
Specific Rotation (α20/D c1 CH2Cl2) 180-200
Appearance White to brown powder
Infrared Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,330.00
inventory 1g
10-20 days ฿2,890.00

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2,6-Bis[4R-4-phenyl-2-oxazolinyl]pyridine
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This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a critical role in facilitating reactions such as hydrogenation, allylic alkylation, and Diels-Alder reactions, where it helps produce chiral compounds with high enantiomeric purity. Its application is significant in the pharmaceutical industry for synthesizing enantiomerically pure drugs. Additionally, it is utilized in organic chemistry research for developing novel catalytic pr

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. It plays a critical role in facilitating reactions such as hydrogenation, allylic alkylation, and Diels-Alder reactions, where it helps produce chiral compounds with high enantiomeric purity. Its application is significant in the pharmaceutical industry for synthesizing enantiomerically pure drugs. Additionally, it is utilized in organic chemistry research for developing novel catalytic processes and studying stereoselective transformations. Its rigid structure and ability to coordinate with metals make it a valuable tool in creating efficient and selective catalysts.

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