3-Bromo-4-nitro-1H-pyrrolo[2,3-b]pyridine
98%
- Product Code: 45242
CAS:
869335-36-4
| Molecular Weight: | 242.0320 g./mol | Molecular Formula: | C₇H₄BrN₃O₂ |
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| EC Number: | MDL Number: | MFCD09880133 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of more complex molecules. Its structure, featuring both bromo and nitro functional groups, makes it a versatile building block for constructing heterocyclic compounds, which are often found in pharmaceuticals and agrochemicals. Researchers leverage its reactivity in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create novel compounds with potential biological activity. Additionally, it is explored in medicinal chemistry for the design of drug candidates targeting various diseases, including cancer and infectious diseases, due to its ability to interact with biological targets. Its application extends to materials science, where it contributes to the synthesis of organic electronic materials and dyes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿918.00 |
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3-Bromo-4-nitro-1H-pyrrolo[2,3-b]pyridine
This compound is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the development of more complex molecules. Its structure, featuring both bromo and nitro functional groups, makes it a versatile building block for constructing heterocyclic compounds, which are often found in pharmaceuticals and agrochemicals. Researchers leverage its reactivity in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create novel compounds with potential biological activity. Additionally, it is explored in medicinal chemistry for the design of drug candidates targeting various diseases, including cancer and infectious diseases, due to its ability to interact with biological targets. Its application extends to materials science, where it contributes to the synthesis of organic electronic materials and dyes.
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