[1,2,3]Thiadiazole-4-carbonyl chloride
97%
- Product Code: 243364
CAS:
4100-17-8
| Molecular Weight: | 148.57 g./mol | Molecular Formula: | C₃HClN₂OS |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03840353 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, argon-filled |
Product Description:
Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its reactivity allows for the introduction of the thiadiazole ring into larger molecules, enhancing biological activity. Commonly employed in the development of herbicides, fungicides, and plant growth regulators due to the thiadiazole core’s ability to interact with biological targets in pests and pathogens. Also utilized in the preparation of specialty polymers and corrosion inhibitors, where its sulfur and nitrogen atoms contribute to metal coordination and material stability. The carbonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing amide and ester linkages in complex molecule assembly.
Sizes / Availability / Pricing:
| Size | Availability | Price | Quantity |
|---|---|---|---|
| 0.500 | 10-20 days | $311.38 |
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[1,2,3]Thiadiazole-4-carbonyl chloride
Used primarily as an intermediate in the synthesis of agrochemicals and pharmaceuticals. Its reactivity allows for the introduction of the thiadiazole ring into larger molecules, enhancing biological activity. Commonly employed in the development of herbicides, fungicides, and plant growth regulators due to the thiadiazole core’s ability to interact with biological targets in pests and pathogens. Also utilized in the preparation of specialty polymers and corrosion inhibitors, where its sulfur and nitrogen atoms contribute to metal coordination and material stability. The carbonyl chloride group readily reacts with amines and alcohols, making it valuable for constructing amide and ester linkages in complex molecule assembly.
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