(R)-1-[Bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]phosphino]-2-[(1R)-1-(dicyclohexylphosphino)ethyl]Ferrocene

95%

Reagent Code: #37377
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CAS Number 1453803-83-2

science Other reagents with same CAS 1453803-83-2

blur_circular Chemical Specifications

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Weight 879.0000 g/mol
Formula C₅₄H₈₀FeO₂P₂
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating ferrocene and bulky phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other stereospecific transformations, enabling the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Its steric and electronic properties enhance catalyst stability and selectivity, making it a valuable tool in organic synthesis.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,790.00

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(R)-1-[Bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]phosphino]-2-[(1R)-1-(dicyclohexylphosphino)ethyl]Ferrocene
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This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating ferrocene and bulky phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other stereospecific transformations, enabling the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Its steric and electronic

This compound is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure, incorporating ferrocene and bulky phosphine groups, makes it highly effective in inducing enantioselectivity. It is commonly employed in hydrogenation, carbon-carbon bond formation, and other stereospecific transformations, enabling the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals. Its steric and electronic properties enhance catalyst stability and selectivity, making it a valuable tool in organic synthesis.

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