(8aR)-18-Hydroxy-8,9-diphenyldiphenanthro[4,3-d:3',4'-f][1,3,2]dioxaphosphepine 18-oxide

98%

Reagent Code: #70406
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CAS Number 871130-18-6

science Other reagents with same CAS 871130-18-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 600.6 g/mol
Formula C₄₀H₂₅O₄P
badge Registry Numbers
MDL Number MFCD09265084
thermostat Physical Properties
Melting Point >300 °C
inventory_2 Storage & Handling
Density 1.44±0.1 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a diphenanthro framework and a phosphine oxide moiety, makes it effective in inducing enantioselectivity in various transformations, such as hydrogenation, cross-coupling, and cycloaddition reactions. It is often employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is critical. Additionally, its stability and ability to coordinate with metals enhance its utility in catalytic systems, enabling the production of optically active compounds with high efficiency and selectivity.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,693.00
(8aR)-18-Hydroxy-8,9-diphenyldiphenanthro[4,3-d:3',4'-f][1,3,2]dioxaphosphepine 18-oxide
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This compound is primarily utilized in organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a diphenanthro framework and a phosphine oxide moiety, makes it effective in inducing enantioselectivity in various transformations, such as hydrogenation, cross-coupling, and cycloaddition reactions. It is often employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is

This compound is primarily utilized in organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its unique structure, featuring a diphenanthro framework and a phosphine oxide moiety, makes it effective in inducing enantioselectivity in various transformations, such as hydrogenation, cross-coupling, and cycloaddition reactions. It is often employed in the synthesis of complex molecules, including pharmaceuticals and fine chemicals, where achieving high enantiomeric purity is critical. Additionally, its stability and ability to coordinate with metals enhance its utility in catalytic systems, enabling the production of optically active compounds with high efficiency and selectivity.

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