(R)-3,3'-Bis[3,5-bis(trifluoromethyl)phenyl]-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol

≥98%,99%e.e.

Reagent Code: #70326
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CAS Number 618854-91-4

science Other reagents with same CAS 618854-91-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 718.6 g/mol
Formula C₃₆H₂₆F₁₂O₂
thermostat Physical Properties
Melting Point 195-196°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure, featuring trifluoromethyl groups and a rigid binaphthol backbone, makes it highly effective in enantioselective reactions, particularly in the formation of chiral centers in organic molecules. It is often employed in transition-metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other transformations requiring high enantiomeric excess. Additionally, its electron-withdrawing trifluoromethyl groups enhance its stability and reactivity in challenging chemical environments, making it a valuable tool in pharmaceutical and fine chemical synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,820.00
inventory 250mg
10-20 days ฿6,550.00

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(R)-3,3'-Bis[3,5-bis(trifluoromethyl)phenyl]-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
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This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure, featuring trifluoromethyl groups and a rigid binaphthol backbone, makes it highly effective in enantioselective reactions, particularly in the formation of chiral centers in organic molecules. It is often employed in transition-metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other transformations requiring high enantiomeric excess. Additionally, its electron-w
This compound is primarily utilized in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure, featuring trifluoromethyl groups and a rigid binaphthol backbone, makes it highly effective in enantioselective reactions, particularly in the formation of chiral centers in organic molecules. It is often employed in transition-metal-catalyzed processes, such as hydrogenation, carbon-carbon bond formation, and other transformations requiring high enantiomeric excess. Additionally, its electron-withdrawing trifluoromethyl groups enhance its stability and reactivity in challenging chemical environments, making it a valuable tool in pharmaceutical and fine chemical synthesis.
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