(S)-1-[(R)-2-(DI-TERT.-BUTYLPHOSPHINO)FERROCENYL]ETHYLBIS(2-METHYLPHENYL)PHOSPHI

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Reagent Code: #37962
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CAS Number 849924-77-2

science Other reagents with same CAS 849924-77-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 570.515 g/mol
Formula C₂₉H₃₉P₂C₅H₅Fe
badge Registry Numbers
MDL Number MFCD08561173
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a ferrocene backbone and sterically demanding phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high optical purity, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitutions, enabling the creation of complex organic compounds with precise stereochemical control. Its robustness and efficiency make it a valuable tool in organic synthesis and industrial processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,440.00
inventory 1g
10-20 days ฿26,352.00
inventory 100mg
10-20 days ฿6,480.00

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(S)-1-[(R)-2-(DI-TERT.-BUTYLPHOSPHINO)FERROCENYL]ETHYLBIS(2-METHYLPHENYL)PHOSPHI
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a ferrocene backbone and sterically demanding phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high optical purity, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, it f

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring a ferrocene backbone and sterically demanding phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high optical purity, which are crucial in the synthesis of pharmaceuticals and fine chemicals. Additionally, it finds application in carbon-carbon bond-forming reactions, such as cross-coupling and allylic substitutions, enabling the creation of complex organic compounds with precise stereochemical control. Its robustness and efficiency make it a valuable tool in organic synthesis and industrial processes.

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