(S)-1-(3,5-Bis(trifluoromethyl)phenyl)-3-(1-(dimethylamino)-3-methylbutan-2-yl)thiourea
98%
- Product Code: 70456
CAS:
1048692-50-7
| Molecular Weight: | 401.41 g./mol | Molecular Formula: | C₁₆H₂₁F₆N₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD23703021 | |
| Melting Point: | 109-110 °C | Boiling Point: | 349.6±52.0 °C |
| Density: | 1.281±0.06 g/cm3 | Storage Condition: | 2-8°C |
Product Description:
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. 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 the design of potent inhibitors for specific protein targets. Researchers often employ it in the synthesis of molecules with potential therapeutic applications, such as antiviral or anticancer agents. Additionally, its chiral center allows for the exploration of stereoselective reactions, contributing to the development of enantiomerically pure drugs. Its applications are largely confined to laboratory settings, where it is used to study reaction mechanisms and optimize synthetic pathways for drug discovery.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,549.00 |
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(S)-1-(3,5-Bis(trifluoromethyl)phenyl)-3-(1-(dimethylamino)-3-methylbutan-2-yl)thiourea
This chemical is primarily utilized in the field of organic synthesis and pharmaceutical research. 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 the design of potent inhibitors for specific protein targets. Researchers often employ it in the synthesis of molecules with potential therapeutic applications, such as antiviral or anticancer agents. Additionally, its chiral center allows for the exploration of stereoselective reactions, contributing to the development of enantiomerically pure drugs. Its applications are largely confined to laboratory settings, where it is used to study reaction mechanisms and optimize synthetic pathways for drug discovery.
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