(2R,2'S,3R,3'R)-3,3'-di-tert-butyl-2,2'-diisopropyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole

≥97% ,≥99% ee

Reagent Code: #96543
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CAS Number 2214207-75-5

science Other reagents with same CAS 2214207-75-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 470.56 g/mol
Formula C₂₈H₄₀O₂P₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to effectively coordinate with transition metals, enhancing the efficiency and selectivity of reactions such as hydrogenation, hydroformylation, and carbon-carbon bond formation. Additionally, it finds application in the development of pharmaceuticals, where precise stereochemistry is essential for the biological activity of drug molecules. Its robust and sterically hindered framework also makes it suitable for use in creating highly selective catalysts for organic transformations.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿6,291.00
100mg
10-20 days ฿17,991.00
(2R,2'S,3R,3'R)-3,3'-di-tert-butyl-2,2'-diisopropyl-2,2',3,3'-tetrahydro-4,4'-bibenzo[d][1,3]oxaphosphole
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This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to effectively coordinate with transition metals, enhancing the efficiency and selectivity of reactions such as hydrogenation, hydroformylation, and carbon-carbon bond formation. Additionally, it finds application in the development of pharmaceuticals, where precise stereochemistry is essential for the biological activity o

This chemical is primarily utilized as a chiral ligand in asymmetric synthesis, particularly in catalytic reactions where enantioselectivity is crucial. Its unique structure allows it to effectively coordinate with transition metals, enhancing the efficiency and selectivity of reactions such as hydrogenation, hydroformylation, and carbon-carbon bond formation. Additionally, it finds application in the development of pharmaceuticals, where precise stereochemistry is essential for the biological activity of drug molecules. Its robust and sterically hindered framework also makes it suitable for use in creating highly selective catalysts for organic transformations.

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