(4S,5S)-N-(3,5-Bis(trifluoromethyl)phenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-2-amine
≥98%,≥99%e.e.
- Product Code: 59741
| Molecular Weight: | 449.4 g./mol | Molecular Formula: | C₂₃H₁₇N₃F₆ |
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| Density: | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry due to its unique structure and properties. It serves as a key intermediate in the development of chiral catalysts, which are essential for asymmetric synthesis reactions. These reactions are crucial in producing enantiomerically pure compounds, particularly in the pharmaceutical industry where the chirality of a drug can significantly impact its efficacy and safety.
Additionally, it is employed in the design and synthesis of novel ligands for metal-catalyzed reactions. Its imidazole core and trifluoromethyl groups enhance its ability to bind to metal centers, making it valuable in catalysis research. The compound’s structural features also make it a candidate for studying enzyme inhibition, particularly in targeting enzymes involved in disease pathways. Its potential applications extend to the development of therapeutic agents, especially in areas requiring high specificity and selectivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿30,132.00 |
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(4S,5S)-N-(3,5-Bis(trifluoromethyl)phenyl)-4,5-diphenyl-4,5-dihydro-1H-imidazol-2-amine
This compound is primarily utilized in the field of organic synthesis and medicinal chemistry due to its unique structure and properties. It serves as a key intermediate in the development of chiral catalysts, which are essential for asymmetric synthesis reactions. These reactions are crucial in producing enantiomerically pure compounds, particularly in the pharmaceutical industry where the chirality of a drug can significantly impact its efficacy and safety.
Additionally, it is employed in the design and synthesis of novel ligands for metal-catalyzed reactions. Its imidazole core and trifluoromethyl groups enhance its ability to bind to metal centers, making it valuable in catalysis research. The compound’s structural features also make it a candidate for studying enzyme inhibition, particularly in targeting enzymes involved in disease pathways. Its potential applications extend to the development of therapeutic agents, especially in areas requiring high specificity and selectivity.
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