(4R,5R)-N-(3,5-Bis(trifluoromethyl)phenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-2-amine

≥98%,≥99%e.e.

Reagent Code: #59720

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 449.4 g/mol
Formula C₂₃H₁₇N₃F₆
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its structure, featuring imidazole and trifluoromethylphenyl groups, makes it effective in facilitating enantioselective transformations, which are crucial in the production of pharmaceuticals and fine chemicals. It is often employed in reactions like hydrogenation, where high selectivity for specific enantiomers is required. Additionally, its stability and unique electronic properties make it suitable for use in advanced material research, particularly in the development of chiral polymers or complexes with potential applications in optoelectronics and catalysis. Its role in enhancing reaction efficiency and selectivity underscores its importance in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿30,132.00

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(4R,5R)-N-(3,5-Bis(trifluoromethyl)phenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-2-amine
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This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its structure, featuring imidazole and trifluoromethylphenyl groups, makes it effective in facilitating enantioselective transformations, which are crucial in the production of pharmaceuticals and fine chemicals. It is often employed in reactions like hydrogenation, where high selectivity for specific enantiomers is required. Additionally, its stability and unique el

This chemical is primarily utilized in the field of organic synthesis, particularly as a chiral ligand or catalyst in asymmetric reactions. Its structure, featuring imidazole and trifluoromethylphenyl groups, makes it effective in facilitating enantioselective transformations, which are crucial in the production of pharmaceuticals and fine chemicals. It is often employed in reactions like hydrogenation, where high selectivity for specific enantiomers is required. Additionally, its stability and unique electronic properties make it suitable for use in advanced material research, particularly in the development of chiral polymers or complexes with potential applications in optoelectronics and catalysis. Its role in enhancing reaction efficiency and selectivity underscores its importance in modern synthetic chemistry.

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