(2S)-1-[(4S)-4,5-Dihydro-4-phenylmethyl-2-oxazolyl]-2-(diphenylphosphino)ferrocene

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Reagent Code: #59665
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CAS Number 541540-58-3

science Other reagents with same CAS 541540-58-3

blur_circular Chemical Specifications

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Weight 539.5 g/mol
Formula C₃₂H₃₈FeNOP
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 diphenylphosphine groups, makes it highly effective in inducing enantioselectivity in various organic transformations.

One key application is in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric excess. This is crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the specific spatial arrangement of atoms can significantly impact the biological activity of the compound.

Additionally, it is employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to create complex organic molecules with precise stereochemistry. Its stability and efficiency in these reactions make it a valuable tool in organic synthesis laboratories.

Overall, this chemical plays a vital role in advancing the field of asymmetric synthesis, enabling the production of enantiomerically pure compounds with significant industrial and academic importance.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿8,964.00
inventory 100mg
10-20 days ฿26,820.00

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(2S)-1-[(4S)-4,5-Dihydro-4-phenylmethyl-2-oxazolyl]-2-(diphenylphosphino)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 diphenylphosphine groups, makes it highly effective in inducing enantioselectivity in various organic transformations.

One key application is in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric excess. This is 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, combining ferrocene and diphenylphosphine groups, makes it highly effective in inducing enantioselectivity in various organic transformations.

One key application is in asymmetric hydrogenation reactions, where it helps produce chiral molecules with high enantiomeric excess. This is crucial in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals, where the specific spatial arrangement of atoms can significantly impact the biological activity of the compound.

Additionally, it is employed in cross-coupling reactions, such as Suzuki-Miyaura and Heck reactions, to create complex organic molecules with precise stereochemistry. Its stability and efficiency in these reactions make it a valuable tool in organic synthesis laboratories.

Overall, this chemical plays a vital role in advancing the field of asymmetric synthesis, enabling the production of enantiomerically pure compounds with significant industrial and academic importance.

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