4-Fluoro-1H-indole-3-carboxylic acid
96%
- Product Code: 59988
CAS:
23077-42-1
| Molecular Weight: | 179.15 g./mol | Molecular Formula: | C₉H₆FNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD09954941 | |
| Melting Point: | Boiling Point: | 422.2±25.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, away from light, dry, sealed |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both an indole ring and a carboxylic acid group, makes it a versatile building block for the development of new drugs, particularly in the synthesis of indole-based pharmaceuticals. It is often employed in the creation of compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its fluorine substitution enhances its reactivity and stability, making it valuable in medicinal chemistry research for optimizing drug candidates.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 0.100 | 10-20 days | £42.75 |
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| 0.250 | 10-20 days | £63.92 |
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| 1.000 | 10-20 days | £159.18 |
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4-Fluoro-1H-indole-3-carboxylic acid
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmacologically active compounds. Its structure, featuring both an indole ring and a carboxylic acid group, makes it a versatile building block for the development of new drugs, particularly in the synthesis of indole-based pharmaceuticals. It is often employed in the creation of compounds with potential anti-inflammatory, anticancer, or antimicrobial properties. Additionally, its fluorine substitution enhances its reactivity and stability, making it valuable in medicinal chemistry research for optimizing drug candidates.
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