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

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Reagent Code: #236828
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CAS Number 2185014-90-6

science Other reagents with same CAS 2185014-90-6

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Storage 2-8°C, Inert Gas

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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cycloheptane backbone and oxazoline rings provide a well-defined chiral environment, making it effective in coordinating to metal centers such as copper or palladium. This complexation enables high enantioselectivity in reactions like cyclopropanations, aldol additions, and Diels-Alder reactions. The compound is especially valued in the synthesis of pharmaceutical intermediates and fine chemicals where control of stereochemistry is critical. Its stability under various reaction conditions enhances its utility across different catalytic systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,720.00
inventory 250mg
10-20 days ฿6,720.00
inventory 1g
10-20 days ฿25,180.00

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(4S,4'S)-2,2'-(Cycloheptane-1,1-diyl)bis(4-phenyl-4,5-dihydrooxazole)
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cycloheptane backbone and oxazoline rings provide a well-defined chiral environment, making it effective in coordinating to metal centers such as copper or palladium. This complexation enables high enantioselectivity in reactions like cyclopropanations, aldol additions, and Diels-Alder reactions. The compound is especially valued in the synthesis of pharmaceutical intermediates and fine chemi
Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its rigid cycloheptane backbone and oxazoline rings provide a well-defined chiral environment, making it effective in coordinating to metal centers such as copper or palladium. This complexation enables high enantioselectivity in reactions like cyclopropanations, aldol additions, and Diels-Alder reactions. The compound is especially valued in the synthesis of pharmaceutical intermediates and fine chemicals where control of stereochemistry is critical. Its stability under various reaction conditions enhances its utility across different catalytic systems.
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