2,3-Bis[(2R,5R)-2,5-diMethylphospholano]-N-(3,5-diMethylphenyl)MaleiMide

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Reagent Code: #40705
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CAS Number 1044553-58-3

science Other reagents with same CAS 1044553-58-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 401.39 g/mol
Formula C₂₄H₃₃NO₂P₂
thermostat Physical Properties
Melting Point 233-239°C
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where it acts as a ligand. It is highly effective in facilitating enantioselective hydrogenation reactions, which are crucial for producing chiral compounds in the pharmaceutical and fine chemical industries. Its unique structure allows for precise control over the stereochemistry of the resulting products, making it valuable in the synthesis of complex molecules with high enantiomeric purity. Additionally, it finds application in the development of advanced materials and catalysts for organic transformations, enhancing efficiency and selectivity in chemical processes.

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inventory 500mg
10-20 days ฿16,830.00

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2,3-Bis[(2R,5R)-2,5-diMethylphospholano]-N-(3,5-diMethylphenyl)MaleiMide
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This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where it acts as a ligand. It is highly effective in facilitating enantioselective hydrogenation reactions, which are crucial for producing chiral compounds in the pharmaceutical and fine chemical industries. Its unique structure allows for precise control over the stereochemistry of the resulting products, making it valuable in the synthesis of complex molecules with high enantiomeric purity. Additionally, i

This chemical is primarily utilized in asymmetric synthesis, particularly in catalytic processes where it acts as a ligand. It is highly effective in facilitating enantioselective hydrogenation reactions, which are crucial for producing chiral compounds in the pharmaceutical and fine chemical industries. Its unique structure allows for precise control over the stereochemistry of the resulting products, making it valuable in the synthesis of complex molecules with high enantiomeric purity. Additionally, it finds application in the development of advanced materials and catalysts for organic transformations, enhancing efficiency and selectivity in chemical processes.

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