1-[3,5-Bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-(dimethylamino)cyclohexyl]thiourea
≥98%,99%e.e.
- Product Code: 70590
CAS:
851477-20-8
| Molecular Weight: | 413.4 g./mol | Molecular Formula: | C₁₇H₂₁F₆N₃S |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, dry |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of biologically active compounds, particularly those targeting enzyme inhibition. Its unique structure, featuring trifluoromethyl groups and a thiourea moiety, makes it valuable in designing molecules with enhanced binding affinity and selectivity. It is often employed in the synthesis of potential drug candidates for conditions such as cancer, inflammation, and infectious diseases. Additionally, its chiral cyclohexylamine component is useful in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to off-white Solid |
| PURITY | 97.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿670.00 |
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| 0.250 | 10-20 days | ฿1,590.00 |
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| 1.000 | 10-20 days | ฿6,260.00 |
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| 5.000 | 10-20 days | ฿10,030.00 |
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1-[3,5-Bis(trifluoromethyl)phenyl]-3-[(1S,2S)-2-(dimethylamino)cyclohexyl]thiourea
This chemical is primarily utilized in the field of organic synthesis and medicinal chemistry. It serves as a key intermediate in the development of biologically active compounds, particularly those targeting enzyme inhibition. Its unique structure, featuring trifluoromethyl groups and a thiourea moiety, makes it valuable in designing molecules with enhanced binding affinity and selectivity. It is often employed in the synthesis of potential drug candidates for conditions such as cancer, inflammation, and infectious diseases. Additionally, its chiral cyclohexylamine component is useful in asymmetric synthesis, contributing to the production of enantiomerically pure compounds.
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