(S)-(-)-2,2'-Bis[di(3,5-xylyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl

98%

Reagent Code: #68654
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CAS Number 362634-22-8

science Other reagents with same CAS 362634-22-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 694.8197 g/mol
Formula C₄₆H₄₈O₂P₂
badge Registry Numbers
MDL Number MFCD09753009
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its high selectivity and efficiency make it valuable in the pharmaceutical industry for synthesizing chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it finds application in fine chemical production, enabling the creation of complex molecules with precise stereochemistry. Its robust structure and ability to form stable complexes with metals enhance its performance in challenging catalytic environments.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿36,342.00
inventory 250mg
10-20 days ฿13,329.00
inventory 100mg
10-20 days ฿6,246.00

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(S)-(-)-2,2'-Bis[di(3,5-xylyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its high selectivity and efficiency make it valuable in the pharmaceutical industry for synthesizing chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it finds

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It plays a critical role in enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its high selectivity and efficiency make it valuable in the pharmaceutical industry for synthesizing chiral intermediates and active pharmaceutical ingredients (APIs) with high enantiomeric purity. Additionally, it finds application in fine chemical production, enabling the creation of complex molecules with precise stereochemistry. Its robust structure and ability to form stable complexes with metals enhance its performance in challenging catalytic environments.

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