(S)-3,3’-Bis(triphenylsilyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol

≥98%,≥99%e.e.

Reagent Code: #65626

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 811.2 g/mol
Formula C₅₆H₅₀O₂Si₂
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a binaphthol core with triphenylsilyl groups, enhances stereoselectivity in various organic reactions, such as hydrogenation, allylic alkylation, and Diels-Alder reactions. It is also employed in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a chiral auxiliary in the preparation of complex molecules, enabling precise control over stereochemistry. Its stability and steric properties make it a valuable tool in advanced synthetic methodologies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿21,861.00

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(S)-3,3’-Bis(triphenylsilyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
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This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a binaphthol core with triphenylsilyl groups, enhances stereoselectivity in various organic reactions, such as hydrogenation, allylic alkylation, and Diels-Alder reactions. It is also employed in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals, agrochemicals, and fine chemicals. A

This chemical is primarily utilized in asymmetric synthesis and catalysis, particularly in the development of chiral ligands for transition metal complexes. Its unique structure, featuring a binaphthol core with triphenylsilyl groups, enhances stereoselectivity in various organic reactions, such as hydrogenation, allylic alkylation, and Diels-Alder reactions. It is also employed in the synthesis of enantiomerically pure compounds, which are crucial in pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it serves as a chiral auxiliary in the preparation of complex molecules, enabling precise control over stereochemistry. Its stability and steric properties make it a valuable tool in advanced synthetic methodologies.

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