4,5-Difluoro-1H-indole
≥95%
- Product Code: 118398
CAS:
247564-63-2
| Molecular Weight: | 153.13 g./mol | Molecular Formula: | C₈H₅F₂N |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD01863154 | |
| Melting Point: | Boiling Point: | 264.5°C at 760 mmHg | |
| Density: | Storage Condition: | -20°C, dry sealed |
Product Description:
4,5-Difluoro-1H-indole is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring fluorine atoms, enhances the metabolic stability and bioavailability of drug candidates, making it valuable in the design of new therapeutic agents. It is particularly relevant in the development of anti-inflammatory, anticancer, and central nervous system (CNS) drugs. Additionally, its unique properties are exploited in organic synthesis to create complex molecules for further biological evaluation. Researchers also utilize it in the study of enzyme interactions and receptor binding due to its ability to mimic natural indole derivatives while offering improved chemical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | $111.59 |
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| 1.000 | 10-20 days | $279.39 |
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| 5.000 | 10-20 days | $1,121.78 |
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| 10.000 | 10-20 days | $1,917.68 |
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4,5-Difluoro-1H-indole
4,5-Difluoro-1H-indole is primarily used in pharmaceutical research and development as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring fluorine atoms, enhances the metabolic stability and bioavailability of drug candidates, making it valuable in the design of new therapeutic agents. It is particularly relevant in the development of anti-inflammatory, anticancer, and central nervous system (CNS) drugs. Additionally, its unique properties are exploited in organic synthesis to create complex molecules for further biological evaluation. Researchers also utilize it in the study of enzyme interactions and receptor binding due to its ability to mimic natural indole derivatives while offering improved chemical properties.
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