(R,R)-()-2,2'-Bis[(S)-(N,N-dimethylamino)(phenyl)methyl]-1,1'-bis(di(2-methylphenyl)phosphino)ferrocene

97%

Reagent Code: #76938
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CAS Number 831226-39-2

science Other reagents with same CAS 831226-39-2

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Weight 876.88 g/mol
Formula C₅₆H₅₈FEN₂P₂
inventory_2 Storage & Handling
Storage room temperature, in an inert gas

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 ferrocene and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high optical purity. Additionally, it is used in carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation, to create complex chiral intermediates for pharmaceuticals and fine chemicals. Its stability and efficiency make it a valuable tool in synthetic organic chemistry for producing enantiomerically pure compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,640.00
inventory 500mg
10-20 days ฿32,400.00

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(R,R)-()-2,2'-Bis[(S)-(N,N-dimethylamino)(phenyl)methyl]-1,1'-bis(di(2-methylphenyl)phosphino)ferrocene
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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 ferrocene and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high optical purity. Additionally, it is used in carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation, to create complex chiral inter

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, featuring ferrocene and phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation reactions, where it helps produce chiral molecules with high optical purity. Additionally, it is used in carbon-carbon bond-forming reactions, such as asymmetric allylic alkylation, to create complex chiral intermediates for pharmaceuticals and fine chemicals. Its stability and efficiency make it a valuable tool in synthetic organic chemistry for producing enantiomerically pure compounds.

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