S)-N-Benzhydryl-2-(3-(3,5-bis(trifluoromethyl)phenyl)thioureido)-N,3,3-trimethylbutanamide
98%
- Product Code: 59671
CAS:
1186602-28-7
| Molecular Weight: | 581.6154792 g./mol | Molecular Formula: | C₂₉H₂₉F₆N₃OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD18827622 | |
| Melting Point: | 193-198 °C | Boiling Point: | 574.7±60.0 °C(Predicted) |
| Density: | 1.289±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a benzhydryl group and trifluoromethylphenyl moiety, makes it suitable for designing compounds that interact with specific biological targets, such as enzymes or receptors. It is often explored in the development of potential therapeutic agents, including those targeting neurological disorders or inflammatory conditions. Additionally, its thioureido group enhances its ability to form stable interactions with proteins, making it valuable in the study of enzyme inhibition or modulation. Researchers also leverage its unique chemical properties to optimize pharmacokinetic profiles, such as improving metabolic stability and bioavailability in drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | $315.97 |
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S)-N-Benzhydryl-2-(3-(3,5-bis(trifluoromethyl)phenyl)thioureido)-N,3,3-trimethylbutanamide
This compound is primarily utilized in the field of medicinal chemistry and drug development, particularly as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a benzhydryl group and trifluoromethylphenyl moiety, makes it suitable for designing compounds that interact with specific biological targets, such as enzymes or receptors. It is often explored in the development of potential therapeutic agents, including those targeting neurological disorders or inflammatory conditions. Additionally, its thioureido group enhances its ability to form stable interactions with proteins, making it valuable in the study of enzyme inhibition or modulation. Researchers also leverage its unique chemical properties to optimize pharmacokinetic profiles, such as improving metabolic stability and bioavailability in drug candidates.
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