6-Bromo-4-nitro-1H-indole
97%
- Product Code: 120660
CAS:
885520-50-3
| Molecular Weight: | 241.04 g./mol | Molecular Formula: | C₈H₅BrN₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07781453 | |
| Melting Point: | Boiling Point: | 402.3±25.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
6-Bromo-4-nitro-1H-indole is primarily used in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of indole-based drugs that target various biological pathways. It is also utilized in research for the development of new therapeutic agents, especially in the fields of oncology and neurology, where indole derivatives are known to exhibit significant biological activity. Additionally, this compound serves as a building block in the synthesis of agrochemicals, contributing to the development of new pesticides and herbicides. Its nitro and bromo functional groups make it a versatile reagent in cross-coupling reactions, which are essential in constructing complex organic molecules.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,881.00 |
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| 0.250 | 10-20 days | ฿3,366.00 |
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| 1.000 | 10-20 days | ฿8,361.00 |
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6-Bromo-4-nitro-1H-indole
6-Bromo-4-nitro-1H-indole is primarily used in organic synthesis as a key intermediate for the development of more complex chemical compounds. Its structure makes it valuable in the synthesis of pharmaceuticals, particularly in the creation of indole-based drugs that target various biological pathways. It is also utilized in research for the development of new therapeutic agents, especially in the fields of oncology and neurology, where indole derivatives are known to exhibit significant biological activity. Additionally, this compound serves as a building block in the synthesis of agrochemicals, contributing to the development of new pesticides and herbicides. Its nitro and bromo functional groups make it a versatile reagent in cross-coupling reactions, which are essential in constructing complex organic molecules.
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