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

≥95%,99%e.e.

Reagent Code: #70363
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CAS Number 1041186-22-4

science Other reagents with same CAS 1041186-22-4

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 compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its structure, featuring chiral centers and bulky triphenylsilyl groups, makes it an effective ligand for transition metal catalysts. It is often employed in the development of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Additionally, it finds application in the synthesis of complex natural products and pharmaceuticals, where high enantiomeric purity is crucial. Its unique steric and electronic properties enhance the selectivity and efficiency of catalytic processes, making it valuable in advanced synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,580.00

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(R)-3,3'-Bis(triphenylsilyl)-5,5',6,6',7,7',8,8'-octahydro-1,1'-bi-2,2'-naphthol
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This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its structure, featuring chiral centers and bulky triphenylsilyl groups, makes it an effective ligand for transition metal catalysts. It is often employed in the development of chiral catalysts for organic transformations, such as hydrogenation, carbon-carbon bond formation, and other stereospecific reactions. Additionally, it finds application in the synthesis of complex natural products and pharmaceuticals, where high enantiomeric purity is crucial. Its unique steric and electronic properties enhance the selectivity and efficiency of catalytic processes, making it valuable in advanced synthetic chemistry.
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