(4R,4'R)-2,2'-(Cyclopentane-1,1-diyl)bis(4-benzyl-4,5-dihydrooxazole)

98%

Reagent Code: #59697
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CAS Number 2005443-99-0

science Other reagents with same CAS 2005443-99-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 388.50 g/mol
Formula C₂₅H₂₈N₂O₂
badge Registry Numbers
MDL Number MFCD32201202
thermostat Physical Properties
Boiling Point 524.0±33.0 °C
inventory_2 Storage & Handling
Density 1.21±0.1 g/cm3
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 enantiomeric excess. Its rigid structure and specific stereochemistry make it effective in controlling the spatial arrangement of reactants, leading to the formation of desired chiral products. This compound is especially valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates, ensuring higher efficacy and reduced side effects. Additionally, it finds application in academic research for developing new asymmetric methodologies and studying chiral induction mechanisms.

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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

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿1,990.00
inventory 250mg
10-20 days ฿8,730.00

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(4R,4'R)-2,2'-(Cyclopentane-1,1-diyl)bis(4-benzyl-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 enantiomeric excess. Its rigid structure and specific stereochemistry make it effective in controlling the spatial arrangement of reactants, leading to the formation of desired chiral products. This compound is especially v

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 enantiomeric excess. Its rigid structure and specific stereochemistry make it effective in controlling the spatial arrangement of reactants, leading to the formation of desired chiral products. This compound is especially valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates, ensuring higher efficacy and reduced side effects. Additionally, it finds application in academic research for developing new asymmetric methodologies and studying chiral induction mechanisms.

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