(11bS)-4-Hydroxy-2,6-bis(4-nitrophenyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide

98%, ee 99%

Reagent Code: #38357
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CAS Number 878111-16-1

science Other reagents with same CAS 878111-16-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 590.49 g/mol
Formula C₃₂H₁₉N₂O₈P
badge Registry Numbers
MDL Number MFCD08274951
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This compound is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its unique structure, featuring a phosphine oxide core and nitroaryl groups, makes it effective in asymmetric catalysis, particularly in reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation or carbon-carbon bond formation, to produce chiral molecules with high optical purity. Additionally, its stability and ability to coordinate with metals make it a valuable tool in the development of pharmaceuticals and fine chemicals, where precise stereochemical control is essential.

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Size Availability Unit Price Quantity
inventory 100 mg
10-20 days ฿4,770.00
inventory 25 mg
10-20 days ฿2,754.00

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(11bS)-4-Hydroxy-2,6-bis(4-nitrophenyl)dinaphtho[2,1-d:1',2'-f][1,3,2]dioxaphosphepine 4-oxide
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This compound is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its unique structure, featuring a phosphine oxide core and nitroaryl groups, makes it effective in asymmetric catalysis, particularly in reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation or carbon-carbon bond formation, to produce chiral molecules with high optical purity. Additionally, its stability and ability to coordinat

This compound is primarily utilized in the field of organic synthesis as a chiral ligand or catalyst. Its unique structure, featuring a phosphine oxide core and nitroaryl groups, makes it effective in asymmetric catalysis, particularly in reactions where enantioselectivity is crucial. It is often employed in transition metal-catalyzed processes, such as hydrogenation or carbon-carbon bond formation, to produce chiral molecules with high optical purity. Additionally, its stability and ability to coordinate with metals make it a valuable tool in the development of pharmaceuticals and fine chemicals, where precise stereochemical control is essential.

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