Methyl 5-chloro-4-fluorothiophene-2-carboxylate
97%
- Product Code: 48746
CAS:
2089319-62-8
| Molecular Weight: | 194.6112 g./mol | Molecular Formula: | C₆H₄ClFO₂S |
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| EC Number: | MDL Number: | MFCD30189030 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both chloro and fluoro substituents, makes it a valuable building block for creating compounds with potential biological activity. In pharmaceuticals, it is often incorporated into drug candidates targeting various diseases, leveraging its ability to enhance the potency and selectivity of the final product. In agrochemicals, it serves as a precursor for developing pesticides or herbicides, where its unique electronic properties can improve the efficacy of the active ingredients. Additionally, it is utilized in organic synthesis for the preparation of thiophene-based derivatives, which are important in material science for creating conductive polymers or organic semiconductors.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.050 | 10-20 days | ฿5,958.00 |
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Methyl 5-chloro-4-fluorothiophene-2-carboxylate
This chemical is primarily used in the pharmaceutical and agrochemical industries as a key intermediate in the synthesis of more complex molecules. Its structure, featuring both chloro and fluoro substituents, makes it a valuable building block for creating compounds with potential biological activity. In pharmaceuticals, it is often incorporated into drug candidates targeting various diseases, leveraging its ability to enhance the potency and selectivity of the final product. In agrochemicals, it serves as a precursor for developing pesticides or herbicides, where its unique electronic properties can improve the efficacy of the active ingredients. Additionally, it is utilized in organic synthesis for the preparation of thiophene-based derivatives, which are important in material science for creating conductive polymers or organic semiconductors.
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