(R)-1-[(R)-tert-Butylphosphinoyl]-2-[(R)-1-(diphenylphosphino)ethyl]ferrocene

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Reagent Code: #37375
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CAS Number 1221745-90-9

science Other reagents with same CAS 1221745-90-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 502.3500 g/mol
Formula C₂₈H₃₂FeOP₂
badge Registry Numbers
MDL Number MFCD22666409
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, combining ferrocene and phosphine groups, allows it to effectively induce chirality in products, making it valuable in the synthesis of enantiomerically pure compounds. It is commonly applied in hydrogenation, hydroformylation, and cross-coupling reactions, where high enantioselectivity is crucial. Its stability and efficiency make it a preferred choice in pharmaceutical and fine chemical industries for producing chiral intermediates and active pharmaceutical ingredients (APIs). Additionally, it is utilized in academic research to develop new catalytic methodologies and explore stereochemical outcomes in organic synthesis.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿4,752.00

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(R)-1-[(R)-tert-Butylphosphinoyl]-2-[(R)-1-(diphenylphosphino)ethyl]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, combining ferrocene and phosphine groups, allows it to effectively induce chirality in products, making it valuable in the synthesis of enantiomerically pure compounds. It is commonly applied in hydrogenation, hydroformylation, and cross-coupling reactions, where high enantioselectivity is crucial. Its stability and efficiency make it a preferred choice i

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, combining ferrocene and phosphine groups, allows it to effectively induce chirality in products, making it valuable in the synthesis of enantiomerically pure compounds. It is commonly applied in hydrogenation, hydroformylation, and cross-coupling reactions, where high enantioselectivity is crucial. Its stability and efficiency make it a preferred choice in pharmaceutical and fine chemical industries for producing chiral intermediates and active pharmaceutical ingredients (APIs). Additionally, it is utilized in academic research to develop new catalytic methodologies and explore stereochemical outcomes in organic synthesis.

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