5-[5-(Trifluoromethyl)isoxazol-3-yl]thiophene-2-sulfonyl chloride
97%
- Product Code: 244813
CAS:
229956-98-3
| Molecular Weight: | 317.69 g./mol | Molecular Formula: | C₈H₃ClF₃NO₃S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00831001 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines or alcohols to form sulfonamides or sulfonate esters, making it valuable in constructing sulfone-based derivatives. It is especially useful in drug discovery for developing kinase inhibitors and other therapeutic agents where the trifluoromethylisoxazole moiety enhances metabolic stability and binding affinity. Also employed in the preparation of functionalized thiophene derivatives for use in materials science, including organic semiconductors and electronic materials.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | $318.81 |
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| 5.000 | 10-20 days | $1,110.65 |
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5-[5-(Trifluoromethyl)isoxazol-3-yl]thiophene-2-sulfonyl chloride
Used as a key intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals and agrochemicals. Its sulfonyl chloride group readily reacts with amines or alcohols to form sulfonamides or sulfonate esters, making it valuable in constructing sulfone-based derivatives. It is especially useful in drug discovery for developing kinase inhibitors and other therapeutic agents where the trifluoromethylisoxazole moiety enhances metabolic stability and binding affinity. Also employed in the preparation of functionalized thiophene derivatives for use in materials science, including organic semiconductors and electronic materials.
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