(S)-(6,6'-Dimethoxy-[1,1'-biphenyl]-2,2'-diyl)bis(dicyclohexylphosphine)

98%

Reagent Code: #37844
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CAS Number 246223-35-8

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 606.3800 g/mol
Formula C₃₈H₅₆O₂P₂
inventory_2 Storage & Handling
Storage room temperature

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 facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its application is crucial in the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals, where achieving high enantiomeric purity is essential. The compound’s robust structure and stereochemical control make it a valuable tool in organic synthesis for producing optically active compounds with high selectivity.

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Test Parameter Specification
Appearance white to off-white powder
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿32,680.00
inventory 50mg
10-20 days ฿7,600.00

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(S)-(6,6'-Dimethoxy-[1,1'-biphenyl]-2,2'-diyl)bis(dicyclohexylphosphine)
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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 facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its application is crucial in the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals, where achieving high enantiomeric purity is essential. The compound’s robust structure and stereochemic

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. Its application is crucial in the synthesis of chiral intermediates for pharmaceuticals, agrochemicals, and fine chemicals, where achieving high enantiomeric purity is essential. The compound’s robust structure and stereochemical control make it a valuable tool in organic synthesis for producing optically active compounds with high selectivity.

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