(S)-1-[(S)-1-(Di-tert-butylphosphino)ethyl]-2-[(S)-phenylphosphinoyl]ferrocene

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Reagent Code: #68670
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CAS Number 1221746-66-2

science Other reagents with same CAS 1221746-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 482.37 g/mol
Formula C₂₆H₃₆FeOP₂
badge Registry Numbers
MDL Number MFCD19105637
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating a ferrocene backbone and chiral phosphine groups, makes it highly effective in inducing enantioselectivity. It is widely applied in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is crucial. For example, it is employed in asymmetric hydrogenation reactions to produce chiral intermediates for drugs. Its robustness and ability to maintain high enantiomeric excess under various conditions make it a valuable tool in organic synthesis. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore stereoselective transformations.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿17,820.00
inventory 50mg
10-20 days ฿4,752.00
inventory 100mg
10-20 days ฿8,982.00

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(S)-1-[(S)-1-(Di-tert-butylphosphino)ethyl]-2-[(S)-phenylphosphinoyl]ferrocene
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating a ferrocene backbone and chiral phosphine groups, makes it highly effective in inducing enantioselectivity. It is widely applied in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is crucial. For example, it is employed in asymmetric hydrogenation reactions to produce chiral int

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating a ferrocene backbone and chiral phosphine groups, makes it highly effective in inducing enantioselectivity. It is widely applied in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over stereochemistry is crucial. For example, it is employed in asymmetric hydrogenation reactions to produce chiral intermediates for drugs. Its robustness and ability to maintain high enantiomeric excess under various conditions make it a valuable tool in organic synthesis. Additionally, it is utilized in academic research to develop new catalytic methodologies and explore stereoselective transformations.

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