(3aR,3a'R,8aS,8a'S)-2,2'-(1,3-diphenylpropane-2,2-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole)

98%, ee 99%

Reagent Code: #36715
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CAS Number 394738-76-2

science Other reagents with same CAS 394738-76-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 510.6249 g/mol
Formula C₃₅H₃₀N₂O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chiral bis(oxazoline) ligand, featuring a rigid indeno-fused structure and specific stereochemistry, is primarily used in asymmetric catalysis for enantioselective organic transformations, such as Diels-Alder reactions, allylic alkylations, and other metal-catalyzed processes. Its design enables high levels of stereocontrol, making it valuable for synthesizing enantiomerically pure compounds in pharmaceutical and fine chemical industries. Additionally, it finds applications in materials science for developing chiral polymers and optoelectronic materials, with ongoing research in nanotechnology and sensor technologies.

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Test Parameter Specification
Appearance White to off-white solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 25 mg
10-20 days ฿5,778.00
inventory 100 mg
10-20 days ฿21,564.00
inventory 5 mg
10-20 days ฿1,584.00

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(3aR,3a'R,8aS,8a'S)-2,2'-(1,3-diphenylpropane-2,2-diyl)bis(3a,8a-dihydro-8H-indeno[1,2-d]oxazole)
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This chiral bis(oxazoline) ligand, featuring a rigid indeno-fused structure and specific stereochemistry, is primarily used in asymmetric catalysis for enantioselective organic transformations, such as Diels-Alder reactions, allylic alkylations, and other metal-catalyzed processes. Its design enables high levels of stereocontrol, making it valuable for synthesizing enantiomerically pure compounds in pharmaceutical and fine chemical industries. Additionally, it finds applications in materials science for

This chiral bis(oxazoline) ligand, featuring a rigid indeno-fused structure and specific stereochemistry, is primarily used in asymmetric catalysis for enantioselective organic transformations, such as Diels-Alder reactions, allylic alkylations, and other metal-catalyzed processes. Its design enables high levels of stereocontrol, making it valuable for synthesizing enantiomerically pure compounds in pharmaceutical and fine chemical industries. Additionally, it finds applications in materials science for developing chiral polymers and optoelectronic materials, with ongoing research in nanotechnology and sensor technologies.

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