Ethyl 5-bromo-3-formyl-1h-indole-2-carboxylate
95%
- Product Code: 71162
CAS:
100123-25-9
| Molecular Weight: | 296.1 g./mol | Molecular Formula: | C₁₂H₁₀BrNO₃ |
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| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, stored in inert gas |
Product Description:
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. Its structure, featuring both bromo and formyl functional groups, makes it a versatile intermediate for constructing complex indole-based compounds. It is often employed in the synthesis of potential drug candidates targeting various diseases, including cancer and neurological disorders. Additionally, it serves as a building block in the preparation of heterocyclic compounds, which are crucial in medicinal chemistry and material science. Its reactivity allows for further modifications, enabling researchers to explore a wide range of chemical transformations.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Pale Yellow Powder |
| PURITY | 94.5-100 |
| PROTON NMR SPECTRUM | Conforms to Structure |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿3,880.00 |
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| 1.000 | 10-20 days | ฿8,660.00 |
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| 5.000 | 10-20 days | ฿29,990.00 |
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Ethyl 5-bromo-3-formyl-1h-indole-2-carboxylate
This compound is primarily utilized in organic synthesis, particularly in the development of pharmaceuticals and biologically active molecules. Its structure, featuring both bromo and formyl functional groups, makes it a versatile intermediate for constructing complex indole-based compounds. It is often employed in the synthesis of potential drug candidates targeting various diseases, including cancer and neurological disorders. Additionally, it serves as a building block in the preparation of heterocyclic compounds, which are crucial in medicinal chemistry and material science. Its reactivity allows for further modifications, enabling researchers to explore a wide range of chemical transformations.
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