(R)-6,6'-Bis(3,5-dichlorophenyl)-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol

≥98%,≥99%e.e.

Reagent Code: #70391

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 542.3 g/mol
Formula C₂₉H₂₀Cl₄O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. Its unique structure, featuring spirobi[indene] and dichlorophenyl groups, makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The compound's ability to induce chirality in catalytic processes enhances the efficiency and selectivity of reactions such as hydrogenation, carbon-carbon bond formation, and oxidation. Additionally, it is explored in advanced material science for creating chiral polymers and frameworks with potential applications in sensors, separation technologies, and optoelectronic devices.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿35,469.00

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(R)-6,6'-Bis(3,5-dichlorophenyl)-2,2',3,3'-tetrahydro-1,1'-spirobi[indene]-7,7'-diol
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This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. Its unique structure, featuring spirobi[indene] and dichlorophenyl groups, makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The compound's ability to induce chirality in catalytic processes enhances the efficiency and selectivity of reactions

This chemical is primarily utilized in the field of asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal catalysts. Its unique structure, featuring spirobi[indene] and dichlorophenyl groups, makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals and fine chemicals. The compound's ability to induce chirality in catalytic processes enhances the efficiency and selectivity of reactions such as hydrogenation, carbon-carbon bond formation, and oxidation. Additionally, it is explored in advanced material science for creating chiral polymers and frameworks with potential applications in sensors, separation technologies, and optoelectronic devices.

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