Methyl 4-bromo-5-formylthiophene-2-carboxylate
95%
- Product Code: 47500
CAS:
648412-59-3
| Molecular Weight: | 249.0900 g./mol | Molecular Formula: | C₇H₅BrO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD11100203 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of complex molecules. It is often employed in the preparation of thiophene-based derivatives, which are significant in pharmaceutical research due to their potential biological activities. The presence of both formyl and ester functional groups allows for further chemical modifications, making it a valuable intermediate in the synthesis of heterocyclic compounds. Additionally, it is used in material science for the creation of organic semiconductors and conductive polymers, where thiophene derivatives play a crucial role in enhancing electronic properties. Its bromo substituent also facilitates cross-coupling reactions, enabling the construction of more elaborate structures for various applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿12,528.00 |
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Methyl 4-bromo-5-formylthiophene-2-carboxylate
This compound is primarily utilized in organic synthesis as a versatile building block for the development of complex molecules. It is often employed in the preparation of thiophene-based derivatives, which are significant in pharmaceutical research due to their potential biological activities. The presence of both formyl and ester functional groups allows for further chemical modifications, making it a valuable intermediate in the synthesis of heterocyclic compounds. Additionally, it is used in material science for the creation of organic semiconductors and conductive polymers, where thiophene derivatives play a crucial role in enhancing electronic properties. Its bromo substituent also facilitates cross-coupling reactions, enabling the construction of more elaborate structures for various applications.
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