(R,R)-2,2-Methylenebis(4-phenyl-2-oxazoline)

97%,99%ee

Reagent Code: #37789
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CAS Number 150639-34-2

science Other reagents with same CAS 150639-34-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.3584 g/mol
Formula C₁₉H₁₈N₂O₂
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 where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds in pharmaceuticals and fine chemicals. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds use in polymer chemistry as a building block for creating chiral polymers with specific properties for advanced materials. Its application extends to the development of catalysts for organic transformations, enhancing efficiency and selectivity in complex synthetic pathways.

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Test Parameter Specification
Appearance Light Yellow Viscous Liquid
Purity (%) 96.5-100%
ee 98.5-100
Specific Rotation [α]20/D (c=1 in Ethanol) (°) 92.8-98.8
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,015.00

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(R,R)-2,2-Methylenebis(4-phenyl-2-oxazoline)
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds in pharmaceuticals and fine chemicals. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds use in polymer chemistry as a building block for crea

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation, to produce optically active compounds in pharmaceuticals and fine chemicals. Its rigid structure and chiral centers make it effective in controlling the stereochemistry of the reaction products. Additionally, it finds use in polymer chemistry as a building block for creating chiral polymers with specific properties for advanced materials. Its application extends to the development of catalysts for organic transformations, enhancing efficiency and selectivity in complex synthetic pathways.

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