(R)-3,3'-Bis(4-(tert-butyl)phenyl)-[1,1'-binaphthalene]-2,2'-diol

98%, ee 99%

Reagent Code: #51416
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CAS Number 309934-84-7

science Other reagents with same CAS 309934-84-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 550.72852 g/mol
Formula C₄₀H₃₈O₂
thermostat Physical Properties
Boiling Point 622.8±50.0 °C
inventory_2 Storage & Handling
Density 1.138±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Its unique structure allows it to induce high enantioselectivity, making it valuable in the production of pharmaceuticals and fine chemicals where specific stereochemistry is crucial. Additionally, it is employed in the development of chiral catalysts for organic transformations, enhancing the efficiency and selectivity of reactions in research and industrial settings.

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Size Availability Unit Price Quantity
inventory 25 mg
10-20 days ฿1,170.00
inventory 250 mg
10-20 days ฿7,353.00
inventory 100 mg
10-20 days ฿3,591.00

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(R)-3,3'-Bis(4-(tert-butyl)phenyl)-[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 such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Its unique structure allows it to induce high enantioselectivity, making it valuable in the production of pharmaceuticals and fine chemicals where specific stereochemistry is crucial. Additionally, it is employed in the development of chiral catalysts for organic transformations, enhancing the efficiency and selectivi

This chemical is primarily used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, carbon-carbon bond formation, and oxidation processes. Its unique structure allows it to induce high enantioselectivity, making it valuable in the production of pharmaceuticals and fine chemicals where specific stereochemistry is crucial. Additionally, it is employed in the development of chiral catalysts for organic transformations, enhancing the efficiency and selectivity of reactions in research and industrial settings.

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