(R)-3,3'-Bis(triphenylsilyl)-[1,1'-binaphthalene]-2,2'-diol

98%

Reagent Code: #230617
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CAS Number 111822-69-6

science Other reagents with same CAS 111822-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 803.1 g/mol
Formula C₅₆H₄₂O₂Si₂
badge Registry Numbers
MDL Number MFCD09265078
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its sterically bulky silyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center when coordinated. Commonly employed in asymmetric allylic alkylation, Diels-Alder reactions, and other carbon–carbon bond-forming reactions where high enantiomeric excess is required. The compound’s rigid binaphthyl backbone and tunable substituents make it effective in promoting asymmetric induction in transition metal-catalyzed processes. Also utilized in the synthesis of chiral pharmaceuticals and fine chemicals where precise stereochemical control is critical.

Available Sizes & Pricing

Size Availability Unit Price Quantity
50mg
10-20 days ฿1,170.00
100mg
10-20 days ฿2,100.00
250mg
10-20 days ฿4,280.00
1g
10-20 days ฿14,850.00
(R)-3,3'-Bis(triphenylsilyl)-[1,1'-binaphthalene]-2,2'-diol
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Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its sterically bulky silyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center when coordinated. Commonly employed in asymmetric allylic alkylation, Diels-Alder reactions, and other carbon–carbon bond-forming reactions where high enantiomeric excess is required. The compound’s rigid binaphthyl backbone and tunable substituents make it effective in p

Used as a chiral ligand in asymmetric catalysis, particularly in enantioselective organic transformations. Its sterically bulky silyl groups enhance stereoselectivity by creating a well-defined chiral environment around the metal center when coordinated. Commonly employed in asymmetric allylic alkylation, Diels-Alder reactions, and other carbon–carbon bond-forming reactions where high enantiomeric excess is required. The compound’s rigid binaphthyl backbone and tunable substituents make it effective in promoting asymmetric induction in transition metal-catalyzed processes. Also utilized in the synthesis of chiral pharmaceuticals and fine chemicals where precise stereochemical control is critical.

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