N-[(1S,2S)-2-aMinocyclohexyl]-3,5-bis(trifluoroMethyl)- BenzenesulfonaMide
98%
- Product Code: 70722
CAS:
313342-21-1
| Molecular Weight: | 390.3444592 g./mol | Molecular Formula: | C₁₄H₁₆F₆N₂O₂S |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. It plays a significant role in the development of pharmaceutical agents, particularly in the creation of small molecule inhibitors that target specific enzymes or receptors. Its structural features, including the trifluoromethyl groups and sulfonamide moiety, contribute to its ability to interact with biological targets, enhancing binding affinity and selectivity. Researchers often employ it in drug discovery programs to explore its potential in treating diseases such as cancer, inflammation, and central nervous system disorders. Additionally, its chiral centers make it valuable in studies involving stereochemistry and the development of enantioselective drugs.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿1,890.00 |
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| 0.250 | 10-20 days | ฿7,398.00 |
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| 1.000 | 10-20 days | ฿22,185.00 |
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N-[(1S,2S)-2-aMinocyclohexyl]-3,5-bis(trifluoroMethyl)- BenzenesulfonaMide
This chemical is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active compounds. It plays a significant role in the development of pharmaceutical agents, particularly in the creation of small molecule inhibitors that target specific enzymes or receptors. Its structural features, including the trifluoromethyl groups and sulfonamide moiety, contribute to its ability to interact with biological targets, enhancing binding affinity and selectivity. Researchers often employ it in drug discovery programs to explore its potential in treating diseases such as cancer, inflammation, and central nervous system disorders. Additionally, its chiral centers make it valuable in studies involving stereochemistry and the development of enantioselective drugs.
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