Ethyl 4-amino-5-methoxy-1,2-dimethyl-1H-indole-3-carboxylate
95%
- Product Code: 50557
CAS:
52535-65-6
| Molecular Weight: | 262.3 g./mol | Molecular Formula: | C₁₄H₁₈N₂O₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03848208 | |
| Melting Point: | 96-98 °C | Boiling Point: | 432.3±40.0 °C(Predicted) |
| Density: | 1.21±0.1 g/cm3(Predicted) | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly in the development of novel indole derivatives. Its structure serves as a key intermediate in the synthesis of more complex molecules, which are often explored for their potential pharmacological activities. Researchers focus on its application in creating compounds with possible anti-inflammatory, anticancer, or antimicrobial properties. Additionally, it is employed in the study of structure-activity relationships (SAR) to optimize the biological efficacy of indole-based drugs. Its role in medicinal chemistry underscores its importance in the discovery and development of new therapeutic agents.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.010 | 10-20 days | $133.35 |
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| 0.050 | 10-20 days | $519.84 |
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Ethyl 4-amino-5-methoxy-1,2-dimethyl-1H-indole-3-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly in the development of novel indole derivatives. Its structure serves as a key intermediate in the synthesis of more complex molecules, which are often explored for their potential pharmacological activities. Researchers focus on its application in creating compounds with possible anti-inflammatory, anticancer, or antimicrobial properties. Additionally, it is employed in the study of structure-activity relationships (SAR) to optimize the biological efficacy of indole-based drugs. Its role in medicinal chemistry underscores its importance in the discovery and development of new therapeutic agents.
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