3-(carboxymethyl)-1-methyl-1H-indole-2-carboxylic acid
95%
- Product Code: 65931
CAS:
58664-93-0
| Molecular Weight: | 233.22 g./mol | Molecular Formula: | C₁₂H₁₁NO₄ |
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| EC Number: | MDL Number: | MFCD00228988 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting inflammation and pain management. Its structural framework is often incorporated into the development of nonsteroidal anti-inflammatory drugs (NSAIDs) due to its potential to inhibit cyclooxygenase enzymes, which play a role in inflammatory processes. Additionally, it is explored in the design of novel indole-based compounds for potential therapeutic applications in treating diseases like arthritis and other inflammatory conditions. Its carboxylic acid groups make it a versatile building block for further chemical modifications, enhancing its utility in drug discovery and development.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,861.00 |
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| 0.250 | 10-20 days | ฿7,020.00 |
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| 1.000 | 10-20 days | ฿14,040.00 |
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3-(carboxymethyl)-1-methyl-1H-indole-2-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting inflammation and pain management. Its structural framework is often incorporated into the development of nonsteroidal anti-inflammatory drugs (NSAIDs) due to its potential to inhibit cyclooxygenase enzymes, which play a role in inflammatory processes. Additionally, it is explored in the design of novel indole-based compounds for potential therapeutic applications in treating diseases like arthritis and other inflammatory conditions. Its carboxylic acid groups make it a versatile building block for further chemical modifications, enhancing its utility in drug discovery and development.
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