(2S,2'S,3S,3'S)-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: #96545
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CAS Number 2207601-12-3

science Other reagents with same CAS 2207601-12-3

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 compound is primarily utilized in the field of asymmetric synthesis as a chiral ligand or catalyst. Its unique stereochemistry makes it highly effective in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in transition metal-catalyzed processes, such as hydrogenation, hydroformylation, and cross-coupling reactions, where high enantiomeric purity of the product is desired. Additionally, its robust structure and steric properties enhance its stability and performance in demanding reaction conditions, making it a valuable tool in the synthesis of pharmaceuticals, fine chemicals, and advanced materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿17,991.00
inventory 25mg
10-20 days ฿6,291.00

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(2S,2'S,3S,3'S)-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 compound is primarily utilized in the field of asymmetric synthesis as a chiral ligand or catalyst. Its unique stereochemistry makes it highly effective in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in transition metal-catalyzed processes, such as hydrogenation, hydroformylation, and cross-coupling reactions, where high enantiomeric purity of the product is desired. Additionally, its robust structure and s

This compound is primarily utilized in the field of asymmetric synthesis as a chiral ligand or catalyst. Its unique stereochemistry makes it highly effective in facilitating enantioselective reactions, particularly in the formation of carbon-carbon and carbon-heteroatom bonds. It is often employed in transition metal-catalyzed processes, such as hydrogenation, hydroformylation, and cross-coupling reactions, where high enantiomeric purity of the product is desired. Additionally, its robust structure and steric properties enhance its stability and performance in demanding reaction conditions, making it a valuable tool in the synthesis of pharmaceuticals, fine chemicals, and advanced materials.

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