Ethyl 3-bromofuran-2-carboxylate
95%
- Product Code: 83651
CAS:
32460-07-4
| Molecular Weight: | 219.03 g./mol | Molecular Formula: | C₇H₇BrO₃ |
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| EC Number: | MDL Number: | MFCD24387450 | |
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| Density: | Storage Condition: | 2-8°C |
Product Description:
Ethyl 3-bromofuran-2-carboxylate finds its primary application in organic synthesis, particularly as a versatile intermediate in the construction of complex molecules. It is commonly used in the development of pharmaceuticals, where its bromine and ester functional groups allow for further chemical modifications, such as cross-coupling reactions or nucleophilic substitutions. This compound is also employed in the synthesis of heterocyclic compounds, which are crucial in medicinal chemistry for designing drugs with specific biological activities. Additionally, it serves as a building block in agrochemical research for creating novel pesticides or herbicides. Its reactivity and structural features make it a valuable tool in academic and industrial laboratories for exploring new chemical pathways.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | €216.07 |
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| 0.250 | 10-20 days | €370.40 |
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| 1.000 | 10-20 days | €740.81 |
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Ethyl 3-bromofuran-2-carboxylate
Ethyl 3-bromofuran-2-carboxylate finds its primary application in organic synthesis, particularly as a versatile intermediate in the construction of complex molecules. It is commonly used in the development of pharmaceuticals, where its bromine and ester functional groups allow for further chemical modifications, such as cross-coupling reactions or nucleophilic substitutions. This compound is also employed in the synthesis of heterocyclic compounds, which are crucial in medicinal chemistry for designing drugs with specific biological activities. Additionally, it serves as a building block in agrochemical research for creating novel pesticides or herbicides. Its reactivity and structural features make it a valuable tool in academic and industrial laboratories for exploring new chemical pathways.
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