N,N'-[(1R,2R)-1,2-diphenyl-1,2-ethanediyl]bis[2-(diphenylphosphino)-BenzaMide

97%

Reagent Code: #70659
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CAS Number 138517-62-1

science Other reagents with same CAS 138517-62-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 788.849602 g/mol
Formula C₅₂H₄₂N₂O₂P₂
thermostat Physical Properties
Boiling Point 900.4±65.0 °C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral compounds. Its structure, featuring diphenylphosphino groups and a chiral backbone, makes it an effective ligand in transition metal-catalyzed reactions. It is often employed in hydrogenation, cross-coupling, and other stereoselective transformations, enabling the production of enantiomerically pure pharmaceuticals, agrochemicals, and fine chemicals. Its ability to induce high enantioselectivity and reactivity in catalytic processes makes it a valuable tool in organic synthesis. Additionally, it finds use in academic and industrial research for developing new catalytic methodologies and optimizing existing ones.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,142.00
inventory 250mg
10-20 days ฿8,532.00

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N,N'-[(1R,2R)-1,2-diphenyl-1,2-ethanediyl]bis[2-(diphenylphosphino)-BenzaMide
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This chemical is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral compounds. Its structure, featuring diphenylphosphino groups and a chiral backbone, makes it an effective ligand in transition metal-catalyzed reactions. It is often employed in hydrogenation, cross-coupling, and other stereoselective transformations, enabling the production of enantiomerically pure pharmaceuticals, agrochemicals, and fine chemicals. Its ability to induce high enantioselectiv

This chemical is primarily utilized in the field of asymmetric catalysis, particularly in the synthesis of chiral compounds. Its structure, featuring diphenylphosphino groups and a chiral backbone, makes it an effective ligand in transition metal-catalyzed reactions. It is often employed in hydrogenation, cross-coupling, and other stereoselective transformations, enabling the production of enantiomerically pure pharmaceuticals, agrochemicals, and fine chemicals. Its ability to induce high enantioselectivity and reactivity in catalytic processes makes it a valuable tool in organic synthesis. Additionally, it finds use in academic and industrial research for developing new catalytic methodologies and optimizing existing ones.

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