2-Bromo-3-iodophenol
97%
- Product Code: 116660
CAS:
863870-88-6
| Molecular Weight: | 298.9 g./mol | Molecular Formula: | C₆H₄BrIO |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD08166322 | |
| Melting Point: | 69-71 °C | Boiling Point: | 290.1±25.0 °C(Predicted) |
| Density: | 2.369±0.06 g/cm3(Predicted) | Storage Condition: | 2-8℃, shading |
Product Description:
2-Bromo-3-iodophenol is primarily used in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in the pharmaceutical industry, where it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs). Its unique halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki and Sonogashira reactions, which are crucial for creating carbon-carbon bonds in drug development. Additionally, it finds applications in material science, where it is used to synthesize specialized polymers and organic compounds with specific electronic or optical properties. Its role in research and development is significant, particularly in the study of halogenated aromatic compounds and their reactivity.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | $97.69 |
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| 0.250 | 10-20 days | $168.12 |
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2-Bromo-3-iodophenol
2-Bromo-3-iodophenol is primarily used in organic synthesis as a versatile intermediate. It is often employed in the preparation of complex molecules, particularly in the pharmaceutical industry, where it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs). Its unique halogenated structure makes it valuable in cross-coupling reactions, such as Suzuki and Sonogashira reactions, which are crucial for creating carbon-carbon bonds in drug development. Additionally, it finds applications in material science, where it is used to synthesize specialized polymers and organic compounds with specific electronic or optical properties. Its role in research and development is significant, particularly in the study of halogenated aromatic compounds and their reactivity.
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