(S)-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: #70526

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 utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. Its unique structure allows it to effectively coordinate with transition metals, such as rhodium or iridium, to facilitate asymmetric hydrogenation reactions. These reactions are crucial in the production of pharmaceuticals, where the creation of specific enantiomers is essential for the desired biological activity. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and fine chemicals, where high enantiomeric purity is required. Its stability and efficiency in catalytic systems make it a valuable tool in organic chemistry research and industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿19,440.00

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(S)-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 utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. Its unique structure allows it to effectively coordinate with transition metals, such as rhodium or iridium, to facilitate asymmetric hydrogenation reactions. These reactions are crucial in the production of pharmaceuticals, where the creation of specific enantiomers is essential for the desired biological activity. Additionally, it is employed in the synthesis of complex organic mo

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in enantioselective synthesis. Its unique structure allows it to effectively coordinate with transition metals, such as rhodium or iridium, to facilitate asymmetric hydrogenation reactions. These reactions are crucial in the production of pharmaceuticals, where the creation of specific enantiomers is essential for the desired biological activity. Additionally, it is employed in the synthesis of complex organic molecules, including natural products and fine chemicals, where high enantiomeric purity is required. Its stability and efficiency in catalytic systems make it a valuable tool in organic chemistry research and industrial applications.

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