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

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Reagent Code: #69779
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CAS Number 2185014-88-2

science Other reagents with same CAS 2185014-88-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 374.48 g/mol
Formula C₂₄H₂₆N₂O₂
badge Registry Numbers
MDL Number MFCD32201208
inventory_2 Storage & Handling
Storage 2-8 ℃, inert gas storage

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 control. Its rigid structure and ability to form stable complexes with metals make it effective in enhancing the efficiency and selectivity of these reactions. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where precise chiral induction is required to achieve desired biological activity or product purity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,149.00
inventory 250mg
10-20 days ฿7,344.00
inventory 1g
10-20 days ฿21,402.00

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(4S,4'S)-2,2'-(Cyclohexane-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 control. Its rigid structure and ability to form stable complexes with metals make it effective in enhancing the efficiency and selectivity of these reactions. Additionally, it finds application in the synthe

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 control. Its rigid structure and ability to form stable complexes with metals make it effective in enhancing the efficiency and selectivity of these reactions. Additionally, it finds application in the synthesis of pharmaceuticals and fine chemicals, where precise chiral induction is required to achieve desired biological activity or product purity.

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