Ethyl 7-bromo-1H-indole-2-carboxylate
95%
- Product Code: 52040
Alias:
Ethyl 7-bromo-2-indolecarboxylate;
CAS:
16732-69-7
| Molecular Weight: | 268.11 g./mol | Molecular Formula: | C₁₁H₁₀BrNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD04972046 | |
| Melting Point: | Boiling Point: | 394.7ºC | |
| Density: | 1.554 g/cm3 | Storage Condition: | Room temperature, dry, sealed |
Product Description:
Ethyl 7-bromo-1H-indole-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex indole derivatives. Its bromo and ester functional groups make it a versatile building block in pharmaceutical research, particularly for the synthesis of compounds with potential biological activity. It is often employed in the construction of indole-based molecules that are explored for their therapeutic properties, such as anti-inflammatory, anticancer, or antimicrobial agents. Additionally, this compound is utilized in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of drug candidates. Its reactivity also allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery programs.
Product Specification:
| Test | Specification |
|---|---|
| Purity | 94.5 100% |
| Appearance | WHITE TO LIGHT YELLOW SOLID |
| NMR | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿1,380.00 |
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| 5.000 | 10-20 days | ฿4,700.00 |
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| 25.000 | 10-20 days | ฿16,670.00 |
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Ethyl 7-bromo-1H-indole-2-carboxylate
Ethyl 7-bromo-1H-indole-2-carboxylate is primarily used in organic synthesis as a key intermediate for the development of more complex indole derivatives. Its bromo and ester functional groups make it a versatile building block in pharmaceutical research, particularly for the synthesis of compounds with potential biological activity. It is often employed in the construction of indole-based molecules that are explored for their therapeutic properties, such as anti-inflammatory, anticancer, or antimicrobial agents. Additionally, this compound is utilized in the study of structure-activity relationships (SAR) to optimize the efficacy and selectivity of drug candidates. Its reactivity also allows for further functionalization, enabling the creation of diverse chemical libraries for drug discovery programs.
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