(4S,4'S)-2,2'-(Cyclohexane-1,1-diyl)bis(4-isopropyl-4,5-dihydrooxazole)

98%

Reagent Code: #59702
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CAS Number 1373357-00-6

science Other reagents with same CAS 1373357-00-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 306.44 g/mol
Formula C₁₈H₃₀N₂O₂
thermostat Physical Properties
Boiling Point 391.8±25.0 °C
inventory_2 Storage & Handling
Density 1.17±0.1 g/cm3
Storage 2-8°C

description Product Description

This chemical is primarily utilized as a chiral bis(oxazoline) ligand in asymmetric synthesis, particularly in catalytic reactions such as copper-catalyzed cyclopropanation, allylic alkylation, and kinetic resolution of epoxides, where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes to produce enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Additionally, it finds application in the preparation of fine chemicals and specialty materials, where precise control over stereochemistry is essential. Its rigid structure and ability to induce high stereoselectivity make it a valuable tool in organic synthesis for achieving complex molecular architectures with desired chiral properties.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿12,600.00

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(4S,4'S)-2,2'-(Cyclohexane-1,1-diyl)bis(4-isopropyl-4,5-dihydrooxazole)
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This chemical is primarily utilized as a chiral bis(oxazoline) ligand in asymmetric synthesis, particularly in catalytic reactions such as copper-catalyzed cyclopropanation, allylic alkylation, and kinetic resolution of epoxides, where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes to produce enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Additionally, it fi

This chemical is primarily utilized as a chiral bis(oxazoline) ligand in asymmetric synthesis, particularly in catalytic reactions such as copper-catalyzed cyclopropanation, allylic alkylation, and kinetic resolution of epoxides, where high enantioselectivity is required. It is often employed in transition metal-catalyzed processes to produce enantiomerically pure compounds, which are crucial in the pharmaceutical industry for the synthesis of active pharmaceutical ingredients (APIs). Additionally, it finds application in the preparation of fine chemicals and specialty materials, where precise control over stereochemistry is essential. Its rigid structure and ability to induce high stereoselectivity make it a valuable tool in organic synthesis for achieving complex molecular architectures with desired chiral properties.

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