(4S,4'S)-2,2'-(Cyclopropane-1,1-diyl)bis(4-phenyl-4,5-dihydrooxazole)

98%

Reagent Code: #59728
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CAS Number 573968-16-8

science Other reagents with same CAS 573968-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.40 g/mol
Formula C₂₁H₂₀N₂O₂
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 with high stereochemical purity. Its rigid cyclopropane backbone and chiral oxazole rings make it effective in controlling the spatial arrangement of reactants, leading to enhanced selectivity and efficiency in the formation of chiral products. This makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates. Additionally, it finds use in academic research for developing new asymmetric methodologies and exploring chiral catalysis mechanisms.

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Test Parameter Specification
APPEARANCE Yellow viscous liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿6,462.00
inventory 50mg
10-20 days ฿25,740.00

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(4S,4'S)-2,2'-(Cyclopropane-1,1-diyl)bis(4-phenyl-4,5-dihydrooxazole)
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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 with high stereochemical purity. Its rigid cyclopropane backbone and chiral oxazole rings make it effective in controlling the spatial arrangement of reactants, leading to enhanced selectivity and efficiency in the formation of chira

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 with high stereochemical purity. Its rigid cyclopropane backbone and chiral oxazole rings make it effective in controlling the spatial arrangement of reactants, leading to enhanced selectivity and efficiency in the formation of chiral products. This makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates. Additionally, it finds use in academic research for developing new asymmetric methodologies and exploring chiral catalysis mechanisms.

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