R-3,3'-di-9-phenanthrenyl-1,1'-Binaphthalene]-2,2'-diol

98%, ee 99%

Reagent Code: #55258
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CAS Number 1058734-56-7

science Other reagents with same CAS 1058734-56-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 638.75 g/mol
Formula C₄₈H₃₀O₂
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in asymmetric synthesis and catalysis due to its chiral binaphthyl structure. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. Its phenanthrenyl groups enhance steric and electronic properties, improving selectivity and efficiency in catalytic processes. Additionally, it is employed in the development of chiral materials and sensors, leveraging its unique optical properties for applications in molecular recognition and detection.

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Size Availability Unit Price Quantity
inventory 100 mg
10-20 days ฿5,220.00
inventory 250 mg
10-20 days ฿10,660.00
inventory 1 g
10-20 days ฿42,760.00

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R-3,3'-di-9-phenanthrenyl-1,1'-Binaphthalene]-2,2'-diol
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This chemical is primarily utilized in asymmetric synthesis and catalysis due to its chiral binaphthyl structure. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. Its phenanthrenyl groups enhance steric and electronic properties, improving selectivity and efficiency in catalytic processes. Additionally, it is employed in the development of chiral materials and sensors, le

This chemical is primarily utilized in asymmetric synthesis and catalysis due to its chiral binaphthyl structure. It serves as a key ligand in transition metal-catalyzed reactions, enabling the production of enantiomerically pure compounds, which are crucial in pharmaceuticals and fine chemicals. Its phenanthrenyl groups enhance steric and electronic properties, improving selectivity and efficiency in catalytic processes. Additionally, it is employed in the development of chiral materials and sensors, leveraging its unique optical properties for applications in molecular recognition and detection.

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