(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-di-1-pyrenyl-[1,1'-binaphthalene]-2,2'-diol

≥95%,99%e.e.

Reagent Code: #65637
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CAS Number 1286189-19-2

science Other reagents with same CAS 1286189-19-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 694.9 g/mol
Formula C₅₂H₃₈O₂
inventory_2 Storage & Handling
Density 1.333±0.06 g/mL
Storage room temperature, dry

description Product Description

This chemical is primarily used in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its unique structure makes it effective as a chiral ligand in transition metal-catalyzed processes, such as hydrogenation, oxidation, and carbon-carbon bond formation. It is also employed in the development of chiral materials and sensors, where its optical properties and stereochemical stability are advantageous. Additionally, it finds application in organic electronics and photochemistry due to its extended aromatic system, which enhances light absorption and charge transfer properties.

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inventory 100mg
10-20 days ฿24,260.00

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(S)-5,5',6,6',7,7',8,8'-Octahydro-3,3'-di-1-pyrenyl-[1,1'-binaphthalene]-2,2'-diol
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This chemical is primarily used in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its unique structure makes it effective as a chiral ligand in transition metal-catalyzed processes, such as hydrogenation, oxidation, and carbon-carbon bond formation. It is also employed in the development of chiral materials and sensors, where its optical properties and stereochemical stability are advantageous. Additionally, it finds application in organic electronics and photochemistry d

This chemical is primarily used in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its unique structure makes it effective as a chiral ligand in transition metal-catalyzed processes, such as hydrogenation, oxidation, and carbon-carbon bond formation. It is also employed in the development of chiral materials and sensors, where its optical properties and stereochemical stability are advantageous. Additionally, it finds application in organic electronics and photochemistry due to its extended aromatic system, which enhances light absorption and charge transfer properties.

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