[1,1'-Binaphthalene]-2,2'-diol,5,5',6,6',7,7',8,8'-octahydro-3,3'-diphenyl-, (1R)-

98%

Reagent Code: #70372
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CAS Number 396134-73-9

science Other reagents with same CAS 396134-73-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 446.5794 g/mol
Formula C₃₂H₃₀O₂
inventory_2 Storage & Handling
Storage 2-8°C, away from light

description Product Description

This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, alkylation, and cycloaddition. Its unique structure allows it to effectively induce chirality in products, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in the development of chiral catalysts for enantioselective transformations, enhancing the efficiency and selectivity of synthetic processes. Its stability and versatility make it a preferred choice in organic chemistry research and industrial applications.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿7,920.00
inventory 100mg
10-20 days ฿23,724.00

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[1,1'-Binaphthalene]-2,2'-diol,5,5',6,6',7,7',8,8'-octahydro-3,3'-diphenyl-, (1R)-
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This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, alkylation, and cycloaddition. Its unique structure allows it to effectively induce chirality in products, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in the development of chiral catalysts for enantioselective transformations, enhancing the efficiency and selectivity of synthetic processes. Its stability and versa

This chemical is widely used as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions such as hydrogenation, alkylation, and cycloaddition. Its unique structure allows it to effectively induce chirality in products, making it valuable in the production of pharmaceuticals and fine chemicals. Additionally, it is employed in the development of chiral catalysts for enantioselective transformations, enhancing the efficiency and selectivity of synthetic processes. Its stability and versatility make it a preferred choice in organic chemistry research and industrial applications.

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