(S)-3-3'-Bis[3,5-bis(trifluoromethyl)phenyl]-1,1'-bi-2-naphthol

≥98%,99%e.e.

Reagent Code: #70534
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CAS Number 849939-13-5

science Other reagents with same CAS 849939-13-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 710.5 g/mol
Formula C₃₆H₁₈F₁₂O₂
thermostat Physical Properties
Melting Point 215-219°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in metal-catalyzed processes, such as asymmetric hydrogenation, carbon-carbon bond formation, and other transformations in organic synthesis. Its unique structure, featuring trifluoromethyl groups, enhances its electron-withdrawing properties and stability, making it effective in challenging catalytic environments. Additionally, it finds application in the preparation of enantiomerically pure pharmaceuticals and fine chemicals, where precise control over stereochemistry is critical. Its robustness and selectivity make it a valuable tool in advanced synthetic chemistry.

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Test Parameter Specification
APPEARANCE White to Yellow Solid, Powder, Crystlas, Crystalline Powder and/or Chunks
Purity (%) 97.5-100
e.e% 98.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,367.00
inventory 250mg
10-20 days ฿5,310.00
inventory 1g
10-20 days ฿15,165.00

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(S)-3-3'-Bis[3,5-bis(trifluoromethyl)phenyl]-1,1'-bi-2-naphthol
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in metal-catalyzed processes, such as asymmetric hydrogenation, carbon-carbon bond formation, and other transformations in organic synthesis. Its unique structure, featuring trifluoromethyl groups, enhances its electron-withdrawing properties and stability, making it effective in challenging catalytic environments. Additionally

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in metal-catalyzed processes, such as asymmetric hydrogenation, carbon-carbon bond formation, and other transformations in organic synthesis. Its unique structure, featuring trifluoromethyl groups, enhances its electron-withdrawing properties and stability, making it effective in challenging catalytic environments. Additionally, it finds application in the preparation of enantiomerically pure pharmaceuticals and fine chemicals, where precise control over stereochemistry is critical. Its robustness and selectivity make it a valuable tool in advanced synthetic chemistry.

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