(2S)-1-[(1S)-1-[Bis(1,1-dimethylethyl)phosphino]ethyl]-2-(di-2-furanylphosphino)ferrocene

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Reagent Code: #36508
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CAS Number 849924-42-1

science Other reagents with same CAS 849924-42-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 522.3800 g/mol
Formula C₂₈H₃₆FeO₂P₂
badge Registry Numbers
MDL Number MFCD08561159
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a ferrocene backbone and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high optical purity. Additionally, it finds application in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it enhances the efficiency and selectivity of the process. Its steric and electronic properties make it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is crucial.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,800.00

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(2S)-1-[(1S)-1-[Bis(1,1-dimethylethyl)phosphino]ethyl]-2-(di-2-furanylphosphino)ferrocene
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This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a ferrocene backbone and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high optical purity. Additionally, it finds application in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it enhances

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a ferrocene backbone and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high optical purity. Additionally, it finds application in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, where it enhances the efficiency and selectivity of the process. Its steric and electronic properties make it a valuable tool in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is crucial.

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