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

98%

Reagent Code: #59730
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CAS Number 1003886-07-4

science Other reagents with same CAS 1003886-07-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 402.53 g/mol
Formula C₂₆H₃₀N₂O₂
badge Registry Numbers
MDL Number MFCD32639830
thermostat Physical Properties
Boiling Point 536.3±33.0 °C
inventory_2 Storage & Handling
Density 1.19±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 chiral compounds with high enantiomeric excess. Its rigid cyclohexane backbone and chiral oxazole moieties make it effective in controlling the stereochemistry of reactions, leading to the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is used in the development of novel catalysts for organic transformations, enhancing the efficiency and selectivity of complex synthetic pathways.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿26,874.00
inventory 10mg
10-20 days ฿7,191.00

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(4S,4'S)-2,2'-(Cyclohexane-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 chiral compounds with high enantiomeric excess. Its rigid cyclohexane backbone and chiral oxazole moieties make it effective in controlling the stereochemistry of reactions, leading to the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additi

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 chiral compounds with high enantiomeric excess. Its rigid cyclohexane backbone and chiral oxazole moieties make it effective in controlling the stereochemistry of reactions, leading to the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is used in the development of novel catalysts for organic transformations, enhancing the efficiency and selectivity of complex synthetic pathways.

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