1-((11bS)-8,9,10,11,12,13,14,15-Octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)pyrrolidine

97%

Reagent Code: #236582
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CAS Number 625090-99-5

science Other reagents with same CAS 625090-99-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 393.47 g/mol
Formula C₂₄H₂₈NO₂P
badge Registry Numbers
MDL Number MFCD27923033
thermostat Physical Properties
Melting Point 67 °C
Boiling Point 561.9±60.0 °C(Predicted)
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as 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 rhodium- and ruthenium-based catalytic systems to achieve efficient stereocontrol.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,040.00
inventory 250mg
10-20 days ฿4,340.00
inventory 1g
10-20 days ฿14,400.00
inventory 5g
10-20 days ฿71,880.00

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1-((11bS)-8,9,10,11,12,13,14,15-Octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepin-4-yl)pyrrolidine
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as 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 rhodium- and ruthenium-based catalytic systems to achieve efficient stereocontrol.

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions such as 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 rhodium- and ruthenium-based catalytic systems to achieve efficient stereocontrol.

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