(S)-2,2'-Bis[bis(3,5-trifluoromethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl

98%

Reagent Code: #37995
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CAS Number 1365531-85-6

science Other reagents with same CAS 1365531-85-6

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scatter_plot Molecular Information
Weight 1186.6427 g/mol
Formula C₄₈H₂₈F₂₄O₄P₂
badge Registry Numbers
MDL Number MFCD19443625
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its electron-rich and sterically demanding structure allows for precise control over the stereochemistry of the reaction products, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The trifluoromethyl groups enhance its stability and reactivity, while the methoxy groups contribute to its solubility and ligand-metal coordination properties.

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inventory 100mg
10-20 days ฿6,732.00

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(S)-2,2'-Bis[bis(3,5-trifluoromethylphenyl)phosphino]-4,4',6,6'-tetramethoxy)-1,1'-biphenyl
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This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its electron-rich and sterically demanding structure allows for precise control over the stereochemistry of the reaction products, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine che

This chemical is primarily used as a chiral ligand in asymmetric catalysis, particularly in transition metal-catalyzed reactions. It is highly effective in facilitating enantioselective transformations, such as hydrogenation, carbon-carbon bond formation, and other organic synthesis processes. Its electron-rich and sterically demanding structure allows for precise control over the stereochemistry of the reaction products, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and fine chemicals. The trifluoromethyl groups enhance its stability and reactivity, while the methoxy groups contribute to its solubility and ligand-metal coordination properties.

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