(11aS)-N,N-Diisopropyl-4,5,6,7-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-amine

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Reagent Code: #236581
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CAS Number 477559-83-4

science Other reagents with same CAS 477559-83-4

blur_circular Chemical Specifications

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Weight 381.45 g/mol
Formula C₂₃H₂₈NO₂P
inventory_2 Storage & Handling
Storage 2-8°C, Sealed

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, bidentate structure enables high enantioselectivity in the synthesis of chiral molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. Commonly employed in palladium- and rhodium-based catalytic systems, it helps achieve high catalytic efficiency and stereochemical control under mild reaction conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,660.00
inventory 250mg
10-20 days ฿11,250.00
inventory 1g
10-20 days ฿30,800.00

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(11aS)-N,N-Diisopropyl-4,5,6,7-tetrahydrodiindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-12-amine
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Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, bidentate structure enables high enantioselectivity in the synthesis of chiral molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. Commonly employed in palladium- and rhodium-based catalytic systems, it helps achieve high catalytic efficiency and stereochemical control under

Used as a chiral ligand in asymmetric catalysis, particularly in transition-metal-catalyzed reactions such as asymmetric hydrogenation and cross-coupling. Its rigid, bidentate structure enables high enantioselectivity in the synthesis of chiral molecules, making it valuable in pharmaceutical and fine chemical industries for producing single-enantiomer compounds. Commonly employed in palladium- and rhodium-based catalytic systems, it helps achieve high catalytic efficiency and stereochemical control under mild reaction conditions.

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