1S,2S-N-[3,5-bis(trifluoromethyl)]benzene sulfonamide-1,2-diphenyl ethylenediamine
97%
- Product Code: 70714
CAS:
313342-22-2
| Molecular Weight: | 488.4459392 g./mol | Molecular Formula: | C₂₂H₁₈F₆N₂O₂S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its structure, featuring chiral centers and trifluoromethyl groups, makes it highly effective as a chiral ligand or catalyst in organic transformations. It is often employed in the synthesis of pharmaceuticals, where achieving high enantiomeric purity is critical. Additionally, its sulfonamide group enhances its stability and reactivity in various chemical environments, making it suitable for use in complex synthetic pathways. The trifluoromethyl groups contribute to its electron-withdrawing properties, which can improve the efficiency of catalytic processes. Overall, it plays a significant role in the development of enantiomerically pure compounds in medicinal chemistry and fine chemical synthesis.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,989.00 |
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1S,2S-N-[3,5-bis(trifluoromethyl)]benzene sulfonamide-1,2-diphenyl ethylenediamine
This compound is primarily utilized in asymmetric synthesis and catalysis, particularly in enantioselective reactions. Its structure, featuring chiral centers and trifluoromethyl groups, makes it highly effective as a chiral ligand or catalyst in organic transformations. It is often employed in the synthesis of pharmaceuticals, where achieving high enantiomeric purity is critical. Additionally, its sulfonamide group enhances its stability and reactivity in various chemical environments, making it suitable for use in complex synthetic pathways. The trifluoromethyl groups contribute to its electron-withdrawing properties, which can improve the efficiency of catalytic processes. Overall, it plays a significant role in the development of enantiomerically pure compounds in medicinal chemistry and fine chemical synthesis.
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