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

≥98%,99%e.e.

Reagent Code: #70355
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CAS Number 309934-86-9

science Other reagents with same CAS 309934-86-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 690.8 g/mol
Formula C₅₂H₃₄O₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily used in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals. It is often employed in transition metal-catalyzed processes, such as hydrogenation, oxidation, and carbon-carbon bond formation, to achieve high enantiomeric purity in the final products. Additionally, its application extends to the development of chiral materials and sensors, where its stereochemical properties are leveraged for selective recognition and separation processes.

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Test Parameter Specification
Appearance White to Yellow Solid
Purity (%) 98-100
Enantiomeric Excess (%) 98.5-100
Specific Rotation ([alpha]20/D C=1g/100ml, CHCl3)(deg) -146--152
MS Conforms to Structure
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,060.00

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(R)-3,3'-Bis[4-(2-naphthalenyl)phenyl]-[1,1'-binaphthalene]-2,2'-diol
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This chemical is primarily used in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals. It is often employed in transition metal-catalyzed processes, such as hydrogenation, oxidation, and carbon-carbon bond formation, to achieve high enantiomeric purity in the final products. Additionally, its application extends to the developm
This chemical is primarily used in asymmetric synthesis as a chiral ligand or catalyst. Its unique structure makes it highly effective in facilitating enantioselective reactions, which are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals. It is often employed in transition metal-catalyzed processes, such as hydrogenation, oxidation, and carbon-carbon bond formation, to achieve high enantiomeric purity in the final products. Additionally, its application extends to the development of chiral materials and sensors, where its stereochemical properties are leveraged for selective recognition and separation processes.
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