Ethyl 4-bromothieno[2,3-c]pyridine-2-carboxylate
97%
- Product Code: 47570
CAS:
1809004-78-1
| Molecular Weight: | 286.15 g./mol | Molecular Formula: | C₁₀H₈BrNO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD30188747 | |
| Melting Point: | Boiling Point: | 382.6°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed away from light |
Product Description:
This compound is primarily used in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its thienopyridine core makes it valuable in the creation of pharmaceuticals, particularly in the research and development of drugs targeting neurological disorders and cardiovascular diseases. The ethyl ester group enhances its reactivity, allowing for further chemical modifications, such as hydrolysis or transesterification, to yield derivatives with potential biological activity. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are often explored for their antimicrobial, anti-inflammatory, and anticancer properties. Its bromine substituent also provides a reactive site for cross-coupling reactions, enabling the construction of diverse molecular frameworks in medicinal chemistry and material science.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | $48.14 |
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| 0.250 | 10-20 days | $80.70 |
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| 1.000 | 10-20 days | $242.09 |
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Ethyl 4-bromothieno[2,3-c]pyridine-2-carboxylate
This compound is primarily used in organic synthesis as a versatile intermediate for the development of more complex chemical structures. Its thienopyridine core makes it valuable in the creation of pharmaceuticals, particularly in the research and development of drugs targeting neurological disorders and cardiovascular diseases. The ethyl ester group enhances its reactivity, allowing for further chemical modifications, such as hydrolysis or transesterification, to yield derivatives with potential biological activity. Additionally, it serves as a building block in the synthesis of heterocyclic compounds, which are often explored for their antimicrobial, anti-inflammatory, and anticancer properties. Its bromine substituent also provides a reactive site for cross-coupling reactions, enabling the construction of diverse molecular frameworks in medicinal chemistry and material science.
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