5-(3-Methylisoxazol-5-yl)thiophene-2-sulfonyl chloride
95%
- Product Code: 211467
CAS:
1282218-14-7
| Molecular Weight: | 263.72 g./mol | Molecular Formula: | C₈H₆ClNO₃S₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD15729904 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, dry, light-proof |
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 and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. It is employed in the development of kinase inhibitors and other targeted therapies in medicinal chemistry. The presence of the methylisoxazole and thiophene rings enhances binding affinity in certain drug candidates, especially those targeting neurological and inflammatory pathways. Also utilized in materials science for designing conjugated systems in organic electronics due to its aromatic and heterocyclic framework.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 100mg | 10-20 days | ฿6,770.00 |
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| 250mg | 10-20 days | ฿9,940.00 |
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| 1g | 10-20 days | ฿25,440.00 |
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5-(3-Methylisoxazol-5-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 and alcohols, making it valuable for constructing sulfonamide and sulfonate ester derivatives. It is employed in the development of kinase inhibitors and other targeted therapies in medicinal chemistry. The presence of the methylisoxazole and thiophene rings enhances binding affinity in certain drug candidates, especially those targeting neurological and inflammatory pathways. Also utilized in materials science for designing conjugated systems in organic electronics due to its aromatic and heterocyclic framework.
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