5-Bromo-3-iodo-4-methylpyridin-2-amine
95%
- Product Code: 120178
CAS:
1150618-04-4
| Molecular Weight: | 312.93 g./mol | Molecular Formula: | C₆H₆BrIN₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD12024445 | |
| Melting Point: | Boiling Point: | 316 °C | |
| Density: | 2.243 g/cm3 | Storage Condition: | 2-8°C, sealed, dry, protected from light |
Product Description:
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique halogenated pyridine core makes it particularly valuable in pharmaceutical research, where it is often employed in the synthesis of potential drug candidates, especially those targeting neurological and infectious diseases. Additionally, the presence of both bromine and iodine atoms allows for further functionalization through various cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse libraries of compounds for biological screening. Its application extends to materials science, where it can be used to design and synthesize novel organic materials with specific electronic or photophysical properties.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $135.01 |
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5-Bromo-3-iodo-4-methylpyridin-2-amine
This compound is primarily utilized in the field of organic synthesis, where it serves as a versatile intermediate for the development of more complex chemical structures. Its unique halogenated pyridine core makes it particularly valuable in pharmaceutical research, where it is often employed in the synthesis of potential drug candidates, especially those targeting neurological and infectious diseases. Additionally, the presence of both bromine and iodine atoms allows for further functionalization through various cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the creation of diverse libraries of compounds for biological screening. Its application extends to materials science, where it can be used to design and synthesize novel organic materials with specific electronic or photophysical properties.
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