Ethyl 6-bromo-5-hydroxy-1-methyl-2-((phenylthio)methyl)-1H-Indole-3-carboxylate
≥95%
- Product Code: 120665
CAS:
131707-24-9
| Molecular Weight: | 420.32 g./mol | Molecular Formula: | C₁₉H₁₈BrNO₃S |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00378136 | |
| Melting Point: | Boiling Point: | 570.6°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of indole-based compounds, which are important in drug discovery due to their biological activity. Specifically, it is used in the synthesis of potential therapeutic agents targeting various diseases, including cancer, inflammation, and neurological disorders. Its structural features, such as the bromo and hydroxyl groups, make it a versatile building block for modifying and optimizing drug candidates. Researchers also explore its applications in creating novel heterocyclic compounds with potential pharmacological properties.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Light Brown Solid |
| Purity (%) | 94.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | €24.01 |
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| 10.000 | 10-20 days | €44.32 |
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| 25.000 | 10-20 days | €79.15 |
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| 100.000 | 10-20 days | €250.89 |
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Ethyl 6-bromo-5-hydroxy-1-methyl-2-((phenylthio)methyl)-1H-Indole-3-carboxylate
This compound is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of indole-based compounds, which are important in drug discovery due to their biological activity. Specifically, it is used in the synthesis of potential therapeutic agents targeting various diseases, including cancer, inflammation, and neurological disorders. Its structural features, such as the bromo and hydroxyl groups, make it a versatile building block for modifying and optimizing drug candidates. Researchers also explore its applications in creating novel heterocyclic compounds with potential pharmacological properties.
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