(S)-4-Phenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
97%,99%ee
- Product Code: 38548
CAS:
1803416-28-5
| Molecular Weight: | 292.2559 g./mol | Molecular Formula: | C₁₅H₁₁F₃N₂O |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD32173539 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a trifluoromethylpyridine moiety and a dihydrooxazole ring, makes it valuable in the development of pharmaceuticals targeting specific enzymes or receptors. It is often employed in the design of inhibitors for therapeutic applications, particularly in areas such as oncology, inflammation, and infectious diseases. Additionally, its chiral center allows for the creation of enantiomerically pure compounds, enhancing the precision and efficacy of drug candidates. Researchers also explore its potential in agrochemical development, leveraging its unique chemical properties to create novel pesticides or herbicides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,529.00 |
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(S)-4-Phenyl-2-(5-(trifluoromethyl)pyridin-2-yl)-4,5-dihydrooxazole
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of biologically active molecules. Its structure, featuring a trifluoromethylpyridine moiety and a dihydrooxazole ring, makes it valuable in the development of pharmaceuticals targeting specific enzymes or receptors. It is often employed in the design of inhibitors for therapeutic applications, particularly in areas such as oncology, inflammation, and infectious diseases. Additionally, its chiral center allows for the creation of enantiomerically pure compounds, enhancing the precision and efficacy of drug candidates. Researchers also explore its potential in agrochemical development, leveraging its unique chemical properties to create novel pesticides or herbicides.
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