Methyl 4-fluoro-1H-indole-3-carboxylate
96%
- Product Code: 46850
CAS:
1220039-52-0
Molecular Weight: | 193.1744 g./mol | Molecular Formula: | C₁₀H₈FNO₂ |
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EC Number: | MDL Number: | MFCD09841615 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
Methyl 4-fluoro-1H-indole-3-carboxylate is widely used in organic synthesis as a key intermediate for the development of pharmaceuticals and bioactive compounds. Its indole core structure makes it valuable in the synthesis of various indole-based drugs, which are known for their diverse biological activities, including anti-inflammatory, antiviral, and anticancer properties. The fluorine substitution enhances the compound's reactivity and bioavailability, making it a preferred choice in medicinal chemistry for designing potent drug candidates. Additionally, it serves as a building block in the preparation of agrochemicals, particularly in the development of herbicides and insecticides, due to its ability to interact with biological targets effectively. Its application extends to research laboratories, where it is utilized in the study of structure-activity relationships to optimize the efficacy of new chemical entities.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,341.00 |
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Methyl 4-fluoro-1H-indole-3-carboxylate
Methyl 4-fluoro-1H-indole-3-carboxylate is widely used in organic synthesis as a key intermediate for the development of pharmaceuticals and bioactive compounds. Its indole core structure makes it valuable in the synthesis of various indole-based drugs, which are known for their diverse biological activities, including anti-inflammatory, antiviral, and anticancer properties. The fluorine substitution enhances the compound's reactivity and bioavailability, making it a preferred choice in medicinal chemistry for designing potent drug candidates. Additionally, it serves as a building block in the preparation of agrochemicals, particularly in the development of herbicides and insecticides, due to its ability to interact with biological targets effectively. Its application extends to research laboratories, where it is utilized in the study of structure-activity relationships to optimize the efficacy of new chemical entities.
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