Ethyl 5-bromo-1-benzo[b]thiophene-2-carboxylate
95%
- Product Code: 86801
CAS:
13771-68-1
| Molecular Weight: | 285.16 g./mol | Molecular Formula: | C₁₁H₉BrO₂S |
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| EC Number: | MDL Number: | MFCD12756246 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | Store at room temperature, away from light, dry and sealed |
Product Description:
This compound is primarily used in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring a benzo[b]thiophene core with a bromo substituent and an ester group, makes it valuable in medicinal chemistry for the synthesis of potential drug candidates. Researchers utilize it in the construction of heterocyclic compounds, which are often explored for their biological activities, such as anti-inflammatory, antimicrobial, or anticancer properties. Additionally, it serves as a building block in material science for the creation of organic semiconductors or luminescent materials due to its conjugated system. The bromo group allows for further functionalization through cross-coupling reactions, enhancing its versatility in synthetic applications.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,656.00 |
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| 1.000 | 10-20 days | ฿4,122.00 |
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| 5.000 | 10-20 days | ฿14,499.00 |
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Ethyl 5-bromo-1-benzo[b]thiophene-2-carboxylate
This compound is primarily used in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring a benzo[b]thiophene core with a bromo substituent and an ester group, makes it valuable in medicinal chemistry for the synthesis of potential drug candidates. Researchers utilize it in the construction of heterocyclic compounds, which are often explored for their biological activities, such as anti-inflammatory, antimicrobial, or anticancer properties. Additionally, it serves as a building block in material science for the creation of organic semiconductors or luminescent materials due to its conjugated system. The bromo group allows for further functionalization through cross-coupling reactions, enhancing its versatility in synthetic applications.
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