Methyl 5-chloro-4-fluoro-1H-indole-2-carboxylate
97%
- Product Code: 48745
CAS:
480450-89-3
| Molecular Weight: | 227.62 g./mol | Molecular Formula: | C₁₀H₇ClFNO₂ |
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| Density: | Storage Condition: | room temperature |
Product Description:
Methyl 5-chloro-4-fluoro-1H-indole-2-carboxylate is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its indole core structure makes it valuable for developing drugs targeting neurological disorders, such as serotonin receptor modulators, which are essential in treating conditions like depression and anxiety. Additionally, it serves as a building block in the creation of anticancer agents, particularly in the design of molecules that inhibit specific enzymes or pathways involved in tumor growth. The compound is also utilized in agrochemical research for developing novel pesticides and herbicides, leveraging its halogenated indole structure to enhance biological activity and stability. Its versatility in organic synthesis further extends to the production of dyes and pigments, where it contributes to the creation of complex aromatic systems with specific optical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿14,400.00 |
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Methyl 5-chloro-4-fluoro-1H-indole-2-carboxylate
Methyl 5-chloro-4-fluoro-1H-indole-2-carboxylate is widely used in the pharmaceutical industry as a key intermediate in the synthesis of various bioactive compounds. Its indole core structure makes it valuable for developing drugs targeting neurological disorders, such as serotonin receptor modulators, which are essential in treating conditions like depression and anxiety. Additionally, it serves as a building block in the creation of anticancer agents, particularly in the design of molecules that inhibit specific enzymes or pathways involved in tumor growth. The compound is also utilized in agrochemical research for developing novel pesticides and herbicides, leveraging its halogenated indole structure to enhance biological activity and stability. Its versatility in organic synthesis further extends to the production of dyes and pigments, where it contributes to the creation of complex aromatic systems with specific optical properties.
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