(S)-2-Amino-4-((trifluoromethyl)thio)butanoic acid
97%
- Product Code: 38291
CAS:
764-52-3
| Molecular Weight: | 203.18 g./mol | Molecular Formula: | C₅H₈F₃NO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07636752 | |
| Melting Point: | Boiling Point: | 260.6°C at 760 mmHg | |
| Density: | 1.45g/cm3 | Storage Condition: | Room temperature, away from light, stored in an inert gas |
Product Description:
This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a trifluoromethylthio group, makes it valuable for designing compounds with enhanced metabolic stability and bioavailability. It is often employed in the creation of potential drug candidates targeting neurological disorders, as the trifluoromethylthio group can influence receptor binding and activity. Additionally, it is used in the study of enzyme mechanisms and as a building block in peptide chemistry, where its chiral center allows for the production of stereospecific compounds. Its applications also extend to agrochemical research, where it contributes to the development of novel pesticides and herbicides with improved efficacy.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | White to Off-white Solid |
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.020 | 10-20 days | ฿34,490.00 |
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(S)-2-Amino-4-((trifluoromethyl)thio)butanoic acid
This compound is primarily utilized in the field of pharmaceutical research and development, where it serves as a key intermediate in the synthesis of various biologically active molecules. Its unique structure, featuring a trifluoromethylthio group, makes it valuable for designing compounds with enhanced metabolic stability and bioavailability. It is often employed in the creation of potential drug candidates targeting neurological disorders, as the trifluoromethylthio group can influence receptor binding and activity. Additionally, it is used in the study of enzyme mechanisms and as a building block in peptide chemistry, where its chiral center allows for the production of stereospecific compounds. Its applications also extend to agrochemical research, where it contributes to the development of novel pesticides and herbicides with improved efficacy.
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