(R)-3,3'-Bis([1,1'-biphenyl]-4-yl)-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol

≥98%,99%e.e.

Reagent Code: #70350
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CAS Number 878049-66-2

science Other reagents with same CAS 878049-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 598.8 g/mol
Formula C₄₄H₃₈O₂
thermostat Physical Properties
Boiling Point 797.7±60.0 °C
inventory_2 Storage & Handling
Density 1.182±0.06 g/mL
Storage room temperature, dry

description Product Description

This compound is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its robust structure and ability to induce high enantiomeric excess (ee) in reactions such as hydrogenation, cross-coupling, and cycloaddition make it a preferred choice in industrial and academic research. Additionally, it is employed in the development of advanced materials, including liquid crystals and polymers, where precise stereochemical control is essential.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿20,080.00

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(R)-3,3'-Bis([1,1'-biphenyl]-4-yl)-5,5',6,6',7,7',8,8'-octahydro-[1,1'-binaphthalene]-2,2'-diol
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This compound is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its robust structure and ability to induce high enantiomeric excess (ee) in reactions such as hydrogenation, cross-coupling, and cycloaddition make it a preferred choice in indust
This compound is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is effective in facilitating the formation of chiral centers in organic molecules, making it valuable in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its robust structure and ability to induce high enantiomeric excess (ee) in reactions such as hydrogenation, cross-coupling, and cycloaddition make it a preferred choice in industrial and academic research. Additionally, it is employed in the development of advanced materials, including liquid crystals and polymers, where precise stereochemical control is essential.
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