(11bR)-4-Hydroxy-2,6-bis(perfluorophenyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

98%

Reagent Code: #229312
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CAS Number 1284293-46-4

science Other reagents with same CAS 1284293-46-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 688.44 g/mol
Formula C₃₂H₁₉F₁₀O₄P
thermostat Physical Properties
Boiling Point 689.8±65.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.65±0.1 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions where high enantioselectivity is required. Its rigid backbone and electron-withdrawing perfluorophenyl groups enhance stability and influence catalyst performance in hydrogenation and cross-coupling reactions. Commonly employed in pharmaceutical synthesis to control stereochemistry during the formation of chiral centers. The phosphorus center coordinates with metals such as palladium, rhodium, or ruthenium, enabling efficient asymmetric induction under mild reaction conditions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
25mg
10-20 days ฿4,480.00
50mg
10-20 days ฿8,150.00
100mg
10-20 days ฿16,280.00
(11bR)-4-Hydroxy-2,6-bis(perfluorophenyl)-8,9,10,11,12,13,14,15-octahydrodinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide
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Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions where high enantioselectivity is required. Its rigid backbone and electron-withdrawing perfluorophenyl groups enhance stability and influence catalyst performance in hydrogenation and cross-coupling reactions. Commonly employed in pharmaceutical synthesis to control stereochemistry during the formation of chiral centers. The phosphorus center coordinates with metals such as palladium, rhodium, or rutheni

Used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions where high enantioselectivity is required. Its rigid backbone and electron-withdrawing perfluorophenyl groups enhance stability and influence catalyst performance in hydrogenation and cross-coupling reactions. Commonly employed in pharmaceutical synthesis to control stereochemistry during the formation of chiral centers. The phosphorus center coordinates with metals such as palladium, rhodium, or ruthenium, enabling efficient asymmetric induction under mild reaction conditions.

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