(2R,2'R,3R,3'R)-3,3'-Di-tert-butyl-4,4'-bis(2,6-dimethoxyphenyl)-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole

97%

Reagent Code: #68609
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CAS Number 1884680-48-1

science Other reagents with same CAS 1884680-48-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 658.70 g/mol
Formula C₃₈H₄₄O₆P₂
badge Registry Numbers
MDL Number MFCD31707597
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and stereochemistry enable it to induce high enantioselectivity in various organic transformations, such as hydrogenation, carbon-carbon bond formation, and other key synthetic processes. It is especially valuable in the pharmaceutical industry for the synthesis of enantiomerically pure compounds, which are crucial for developing drugs with specific biological activities. Additionally, its stability and efficiency make it a preferred choice in academic and industrial research for exploring new catalytic methodologies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿35,073.00
inventory 100mg
10-20 days ฿15,786.00

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(2R,2'R,3R,3'R)-3,3'-Di-tert-butyl-4,4'-bis(2,6-dimethoxyphenyl)-2,2',3,3'-tetrahydro-2,2'-bibenzo[d][1,3]oxaphosphole
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This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and stereochemistry enable it to induce high enantioselectivity in various organic transformations, such as hydrogenation, carbon-carbon bond formation, and other key synthetic processes. It is especially valuable in the pharmaceutical industry for the synthesis of enantiomerically pure compounds, which are crucial for developing drugs with specific bi

This chemical is primarily utilized as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and stereochemistry enable it to induce high enantioselectivity in various organic transformations, such as hydrogenation, carbon-carbon bond formation, and other key synthetic processes. It is especially valuable in the pharmaceutical industry for the synthesis of enantiomerically pure compounds, which are crucial for developing drugs with specific biological activities. Additionally, its stability and efficiency make it a preferred choice in academic and industrial research for exploring new catalytic methodologies.

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