(R)-1-(R)-2-[Di(2-furyl)phosphino]ferrocenylethylbis(2-methylphenyl)phosphine

98%,99%ee

Reagent Code: #37378
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CAS Number 849924-73-8

science Other reagents with same CAS 849924-73-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 590.4100 g/mol
Formula C₃₄H₃₂FeO₂P₂
badge Registry Numbers
MDL Number MFCD08561168
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, incorporating ferrocene and phosphine groups, makes it highly effective in inducing enantioselectivity in various organic transformations. One of its key applications is in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric purity, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to create complex organic compounds with precise stereochemistry. Its stability and versatility make it a valuable tool in modern synthetic organic chemistry.

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Test Parameter Specification
Appearance Orange solid
Purity (%) 97.5-100
ee 98.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,799.00

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(R)-1-(R)-2-[Di(2-furyl)phosphino]ferrocenylethylbis(2-methylphenyl)phosphine
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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 ferrocene and phosphine groups, makes it highly effective in inducing enantioselectivity in various organic transformations. One of its key applications is in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric purity, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fin

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating ferrocene and phosphine groups, makes it highly effective in inducing enantioselectivity in various organic transformations. One of its key applications is in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric purity, which are crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to create complex organic compounds with precise stereochemistry. Its stability and versatility make it a valuable tool in modern synthetic organic chemistry.

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