Ethyl 1-methyl-1H-indazole-3-carboxylate
95%
- Product Code: 83115
CAS:
220488-05-1
| Molecular Weight: | 204.23 g./mol | Molecular Formula: | C₁₁H₁₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07368499 | |
| Melting Point: | 58 °C | Boiling Point: | 326.5±15.0 °C(Predicted) |
| Density: | 1.19±0.1 g/cm3(Predicted) | Storage Condition: | room temperature |
Product Description:
Ethyl 1-methyl-1H-indazole-3-carboxylate is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting central nervous system disorders. Its indazole core structure is often incorporated into molecules designed to interact with specific receptors or enzymes, making it valuable in the creation of potential therapeutic agents. Additionally, this compound is explored in medicinal chemistry for its role in developing inhibitors or modulators of protein-protein interactions, which are crucial in treating diseases like cancer and inflammation. Its ester functional group also allows for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿9,000.00 |
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| 0.250 | 10-20 days | ฿17,280.00 |
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| 1.000 | 10-20 days | ฿43,200.00 |
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Ethyl 1-methyl-1H-indazole-3-carboxylate
Ethyl 1-methyl-1H-indazole-3-carboxylate is primarily utilized in the field of pharmaceutical research and development. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting central nervous system disorders. Its indazole core structure is often incorporated into molecules designed to interact with specific receptors or enzymes, making it valuable in the creation of potential therapeutic agents. Additionally, this compound is explored in medicinal chemistry for its role in developing inhibitors or modulators of protein-protein interactions, which are crucial in treating diseases like cancer and inflammation. Its ester functional group also allows for further chemical modifications, enabling the creation of diverse derivatives for drug discovery and optimization.
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