4-Bromo-5,7-difluoro-1H-indole
97%
- Product Code: 47469
CAS:
1381878-59-6
| Molecular Weight: | 232.02 g./mol | Molecular Formula: | C₈H₄BrF₂N |
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| EC Number: | MDL Number: | MFCD23133073 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, store under inert gas |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex chemical structures. Its unique halogenated indole core makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential biological activity. Researchers often employ it in the design of molecules targeting specific enzymes or receptors, leveraging its bromo and fluoro substituents to enhance binding affinity and selectivity. Additionally, it is explored in the development of agrochemicals, where its structural features contribute to the optimization of pesticidal or herbicidal properties. Its versatility in chemical reactions, such as cross-coupling and functional group transformations, further expands its utility in medicinal and industrial chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿4,725.00 |
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| 0.250 | 10-20 days | ฿9,450.00 |
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4-Bromo-5,7-difluoro-1H-indole
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate for the development of more complex chemical structures. Its unique halogenated indole core makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of compounds with potential biological activity. Researchers often employ it in the design of molecules targeting specific enzymes or receptors, leveraging its bromo and fluoro substituents to enhance binding affinity and selectivity. Additionally, it is explored in the development of agrochemicals, where its structural features contribute to the optimization of pesticidal or herbicidal properties. Its versatility in chemical reactions, such as cross-coupling and functional group transformations, further expands its utility in medicinal and industrial chemistry.
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