(R)-3,3'-Bis(4-chlorophenyl)-[1,1'-binaphthalene]-2,2'-diol

≥98%,99%e.e.

Reagent Code: #70333
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CAS Number 851615-05-9

science Other reagents with same CAS 851615-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 507.4 g/mol
Formula C₃₂H₂₀Cl₂O₂
thermostat Physical Properties
Boiling Point 611.4±50.0 °C
inventory_2 Storage & Handling
Density 1.355±0.06 g/mL
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 often employed in the formation of chiral catalysts for organic transformations, such as asymmetric hydrogenation, carbon-carbon bond formation, and oxidation reactions. Its binaphthol structure provides a rigid framework that enhances stereochemical control, making it valuable in the production of pharmaceuticals and fine chemicals where specific enantiomers are desired. Additionally, it has been explored in materials science for the development of chiral polymers and liquid crystals, which have applications in displays and advanced optical devices.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,490.00

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(R)-3,3'-Bis(4-chlorophenyl)-[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 often employed in the formation of chiral catalysts for organic transformations, such as asymmetric hydrogenation, carbon-carbon bond formation, and oxidation reactions. Its binaphthol structure provides a rigid framework that enhances stereochemical control, making it valuable in the production of pharmaceuticals and fine chemicals where specifi

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where high enantioselectivity is required. It is often employed in the formation of chiral catalysts for organic transformations, such as asymmetric hydrogenation, carbon-carbon bond formation, and oxidation reactions. Its binaphthol structure provides a rigid framework that enhances stereochemical control, making it valuable in the production of pharmaceuticals and fine chemicals where specific enantiomers are desired. Additionally, it has been explored in materials science for the development of chiral polymers and liquid crystals, which have applications in displays and advanced optical devices.

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