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

≥98%

Reagent Code: #38651
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CAS Number 210842-74-3

science Other reagents with same CAS 210842-74-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 820.76 g/mol
Formula C₅₂H₅₀FeN₂P₂
badge Registry Numbers
MDL Number MFCD04117705
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, a process crucial for producing chiral molecules in pharmaceuticals and fine chemicals. Its unique structure allows for precise control over the stereochemistry of the reaction, enabling the synthesis of enantiomerically pure compounds. Additionally, it is employed in cross-coupling reactions and other transformations where high selectivity and efficiency are required. Its application extends to the development of advanced materials and agrochemicals, where chiral specificity is essential.

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Test Parameter Specification
Appearance Off-white to Light yellow to Yellow Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 20mg
10-20 days ฿4,419.00
inventory 50mg
10-20 days ฿3,300.00
inventory 250mg
10-20 days ฿6,850.00
inventory 1g
10-20 days ฿26,880.00

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(S,S)-(-)-2,2'-Bis[(R)-(N,N-dimethylamino)(phenyl)methyl]-1,1'-bis(diphenylphosphino)ferrocene
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, a process crucial for producing chiral molecules in pharmaceuticals and fine chemicals. Its unique structure allows for precise control over the stereochemistry of the reaction, enabling the synthesis of enantiomerically pure compounds. Additionally, it is employed in cross-coupling reactions and other transformatio

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in enantioselective hydrogenation, a process crucial for producing chiral molecules in pharmaceuticals and fine chemicals. Its unique structure allows for precise control over the stereochemistry of the reaction, enabling the synthesis of enantiomerically pure compounds. Additionally, it is employed in cross-coupling reactions and other transformations where high selectivity and efficiency are required. Its application extends to the development of advanced materials and agrochemicals, where chiral specificity is essential.

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