(1S)-5,5',6,6',7,7',8,8'-octahydro-3,3'-bis[2,4,6-tris(1-Methylethyl)phenyl]-[1,1'-Binaphthalene]-2,2'-diol

98%

Reagent Code: #65641
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CAS Number 1197214-47-3

science Other reagents with same CAS 1197214-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 699.06 g/mol
Formula C₅₀H₆₆O₂
thermostat Physical Properties
Boiling Point 735.8±60.0 °C
inventory_2 Storage & Handling
Density 1.033±0.06 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in the formation of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its unique structure enhances the selectivity and efficiency of these processes, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additionally, it is used in research and development to explore new catalytic systems and improve existing methodologies in organic chemistry.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿6,750.00
inventory 50mg
10-20 days ฿26,982.00

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(1S)-5,5',6,6',7,7',8,8'-octahydro-3,3'-bis[2,4,6-tris(1-Methylethyl)phenyl]-[1,1'-Binaphthalene]-2,2'-diol
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This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in the formation of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its unique structure enhances the selectivity and efficiency of these processes, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additio

This compound is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. It is often employed in the formation of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Its unique structure enhances the selectivity and efficiency of these processes, making it valuable in the production of pharmaceuticals, fine chemicals, and agrochemicals. Additionally, it is used in research and development to explore new catalytic systems and improve existing methodologies in organic chemistry.

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