Ethyl 4-bromothiophene-3-carboxylate
95%
- Product Code: 94339
CAS:
224449-33-6
| Molecular Weight: | 235.10 g./mol | Molecular Formula: | C₇H₇BrO₂S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD14584478 | |
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| Density: | Storage Condition: | Room temperature, away from light, dry, sealed |
Product Description:
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. It is often employed in the preparation of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. The bromine atom in the structure makes it a valuable intermediate for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in medicinal chemistry to create diverse chemical libraries. Additionally, its thiophene moiety is significant in materials science, where it contributes to the development of organic semiconductors and conductive polymers used in electronic devices. The ester group further allows for functionalization, enabling its use in the design of agrochemicals or specialty chemicals.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,853.00 |
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| 0.250 | 10-20 days | ฿4,266.00 |
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| 1.000 | 10-20 days | ฿10,656.00 |
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Ethyl 4-bromothiophene-3-carboxylate
This compound is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. It is often employed in the preparation of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. The bromine atom in the structure makes it a valuable intermediate for cross-coupling reactions, such as Suzuki or Heck reactions, which are widely used in medicinal chemistry to create diverse chemical libraries. Additionally, its thiophene moiety is significant in materials science, where it contributes to the development of organic semiconductors and conductive polymers used in electronic devices. The ester group further allows for functionalization, enabling its use in the design of agrochemicals or specialty chemicals.
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