(11bR)-2,6-Bis(diphenylphosphino)-N,N-dimethyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine

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Reagent Code: #68586
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CAS Number 913617-04-6

science Other reagents with same CAS 913617-04-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 727.7048 g/mol
Formula C₄₆H₃₆NO₂P₃
badge Registry Numbers
MDL Number MFCD09750461
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and chiral environment make it highly effective in enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where controlling the stereochemistry of the product is crucial. The compound’s ability to induce high enantioselectivity and yield makes it a valuable tool in organic synthesis, especially for producing optically active compounds. Additionally, its stability and compatibility with various metal catalysts enhance its utility in industrial and academic research settings.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,853.00
inventory 250mg
10-20 days ฿10,692.00
inventory 1g
10-20 days ฿34,452.00

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(11bR)-2,6-Bis(diphenylphosphino)-N,N-dimethyldinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-amine
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and chiral environment make it highly effective in enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where controlling the stereochemistry of the product is crucial. The compound’s ability to induce high enantioselectivity

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. Its unique structure and chiral environment make it highly effective in enantioselective transformations, such as hydrogenation, cross-coupling, and allylic substitution reactions. It is often employed in the synthesis of pharmaceuticals and fine chemicals, where controlling the stereochemistry of the product is crucial. The compound’s ability to induce high enantioselectivity and yield makes it a valuable tool in organic synthesis, especially for producing optically active compounds. Additionally, its stability and compatibility with various metal catalysts enhance its utility in industrial and academic research settings.

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