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

98%

Reagent Code: #59729
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CAS Number 1003886-01-8

science Other reagents with same CAS 1003886-01-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 360.45 g/mol
Formula C₂₃H₂₄N₂O₂
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 processes where enantioselectivity is crucial. It is often employed in transition metal-catalyzed reactions, such as hydrogenation, to produce chiral molecules with high optical purity. Its unique structure, featuring a cyclopropane core and dihydrooxazole rings, allows for effective coordination with metal centers, enhancing the stereochemical control of the reaction. This makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates. Additionally, it can be used in the development of advanced materials and fine chemicals where precise chiral induction is required.

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

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(4S,4'S)-2,2'-(Cyclopropane-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 processes where enantioselectivity is crucial. It is often employed in transition metal-catalyzed reactions, such as hydrogenation, to produce chiral molecules with high optical purity. Its unique structure, featuring a cyclopropane core and dihydrooxazole rings, allows for effective coordination with metal centers, enhancing the stereochemical control of the reaction. This makes it valuable in the p

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic processes where enantioselectivity is crucial. It is often employed in transition metal-catalyzed reactions, such as hydrogenation, to produce chiral molecules with high optical purity. Its unique structure, featuring a cyclopropane core and dihydrooxazole rings, allows for effective coordination with metal centers, enhancing the stereochemical control of the reaction. This makes it valuable in the pharmaceutical industry for synthesizing enantiomerically pure drugs and intermediates. Additionally, it can be used in the development of advanced materials and fine chemicals where precise chiral induction is required.

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