Ethyl 3-amino-7-bromobenzofuran-2-carboxylate
95%
- Product Code: 121146
CAS:
1823241-41-3
| Molecular Weight: | 284.11 g./mol | Molecular Formula: | C₁₁H₁₀BrNO₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD21609332 | |
| Melting Point: | Boiling Point: | 382.0±37.0 °C(Predicted) | |
| Density: | 1.585±0.06 g/cm3(Predicted) | Storage Condition: | 2-8°C, dry, sealed |
Product Description:
Ethyl 3-amino-7-bromobenzofuran-2-carboxylate is primarily utilized in organic synthesis as a key intermediate for the development of pharmaceuticals and bioactive compounds. Its structure, featuring both amino and bromo functional groups, makes it a versatile building block in the synthesis of heterocyclic compounds. It is often employed in the preparation of benzofuran derivatives, which are known for their potential therapeutic properties, including anti-inflammatory, antimicrobial, and anticancer activities. Additionally, this compound is used in research settings to explore novel drug candidates and to study structure-activity relationships in medicinal chemistry. Its application extends to the development of fluorescent probes and dyes due to the benzofuran core's ability to exhibit photophysical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿16,974.00 |
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| 1.000 | 10-20 days | ฿38,052.00 |
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Ethyl 3-amino-7-bromobenzofuran-2-carboxylate
Ethyl 3-amino-7-bromobenzofuran-2-carboxylate is primarily utilized in organic synthesis as a key intermediate for the development of pharmaceuticals and bioactive compounds. Its structure, featuring both amino and bromo functional groups, makes it a versatile building block in the synthesis of heterocyclic compounds. It is often employed in the preparation of benzofuran derivatives, which are known for their potential therapeutic properties, including anti-inflammatory, antimicrobial, and anticancer activities. Additionally, this compound is used in research settings to explore novel drug candidates and to study structure-activity relationships in medicinal chemistry. Its application extends to the development of fluorescent probes and dyes due to the benzofuran core's ability to exhibit photophysical properties.
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