1,3-Dibromo-5-fluoro-2-iodobenzene
98%
- Product Code: 114139
Alias:
2,6-Dibromo-4-fluoroiodobenzene
CAS:
62720-29-0
| Molecular Weight: | 379.8 g./mol | Molecular Formula: | C₆H₂Br₂FI |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00042232 | |
| Melting Point: | 134-137 °C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This compound is primarily used as a versatile intermediate in organic synthesis, particularly in the development of complex molecules for pharmaceuticals and agrochemicals. Its unique halogen substitution pattern allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki, Sonogashira, or Buchwald-Hartwig couplings. These reactions are crucial for constructing aromatic frameworks in drug discovery and material science. Additionally, it serves as a building block for synthesizing fluorinated and iodinated compounds, which are often explored for their biological activity or use in imaging agents. Its stability and reactivity make it a preferred choice in research and industrial applications.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point | 133-138 |
| Purity (GC) | 98-100 |
| Appearance | White To Light Brown |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿360.00 |
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| 5.000 | 10-20 days | ฿1,000.00 |
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| 25.000 | 10-20 days | ฿3,860.00 |
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1,3-Dibromo-5-fluoro-2-iodobenzene
This compound is primarily used as a versatile intermediate in organic synthesis, particularly in the development of complex molecules for pharmaceuticals and agrochemicals. Its unique halogen substitution pattern allows for selective functionalization, making it valuable in cross-coupling reactions such as Suzuki, Sonogashira, or Buchwald-Hartwig couplings. These reactions are crucial for constructing aromatic frameworks in drug discovery and material science. Additionally, it serves as a building block for synthesizing fluorinated and iodinated compounds, which are often explored for their biological activity or use in imaging agents. Its stability and reactivity make it a preferred choice in research and industrial applications.
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