(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis(3,5-di-tert-butyl-4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol

≥95%,≥99%e.e.

Reagent Code: #70322

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 731.1 g/mol
Formula C₅₀H₆₆O₄
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical 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 steric properties enhance the stability and efficiency of metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Additionally, it is employed in the development of advanced materials and as a component in chiral catalysts for industrial applications.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿28,341.00

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(R)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-bis(3,5-di-tert-butyl-4-methoxyphenyl)-[1,1'-binaphthalene]-2,2'-diol
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This chemical 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 steric properties enhance the stability and efficiency of metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and oxidation

This chemical 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 steric properties enhance the stability and efficiency of metal-catalyzed reactions, such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Additionally, it is employed in the development of advanced materials and as a component in chiral catalysts for industrial applications.

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