(R)-()-2,2'-Bis[di(3,5-di-t-butylphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl

98%

Reagent Code: #68640
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CAS Number 192138-05-9

science Other reagents with same CAS 192138-05-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1031.4576 g/mol
Formula C₇₀H₉₆O₂P₂
badge Registry Numbers
MDL Number MFCD09753001
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in hydrogenation reactions. It is highly effective in synthesizing enantiomerically pure compounds, which are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its sterically hindered structure and electron-rich properties enhance selectivity and efficiency in catalytic processes. Additionally, it is employed in the development of advanced materials and in research focused on understanding stereochemical control in organic synthesis.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿40,779.00
inventory 100mg
10-20 days ฿6,318.00
inventory 250mg
10-20 days ฿11,124.00

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(R)-()-2,2'-Bis[di(3,5-di-t-butylphenyl)phosphino]-6,6'-dimethoxy-1,1'-biphenyl
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This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in hydrogenation reactions. It is highly effective in synthesizing enantiomerically pure compounds, which are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its sterically hindered structure and electron-rich properties enhance selectivity and efficiency in catalytic processes. Additionally, it is employed in the development of advanced materials and in research focused on understanding

This chemical is widely used as a chiral ligand in asymmetric catalysis, particularly in hydrogenation reactions. It is highly effective in synthesizing enantiomerically pure compounds, which are crucial in the production of pharmaceuticals, agrochemicals, and fine chemicals. Its sterically hindered structure and electron-rich properties enhance selectivity and efficiency in catalytic processes. Additionally, it is employed in the development of advanced materials and in research focused on understanding stereochemical control in organic synthesis.

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