1,3-Dibromo-2-(bromomethyl)-5-fluorobenzene
97%
- Product Code: 38932
CAS:
1804933-11-6
| Molecular Weight: | 346.82 g./mol | Molecular Formula: | C₇H₄Br₃F |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD28784743 | |
| Melting Point: | Boiling Point: | 302.8±37.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed |
Product Description:
This chemical is primarily utilized in organic synthesis as a versatile building block for the construction of complex molecules. Its multiple reactive sites, including bromine atoms and a fluorine substituent, make it valuable for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. The presence of the fluorine atom can enhance the biological activity and metabolic stability of the resulting compounds, making it particularly useful in drug discovery. Additionally, it serves as an intermediate in the production of specialty chemicals and materials, including polymers and liquid crystals, due to its ability to introduce specific functional groups into molecular frameworks.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿8,469.00 |
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| 0.250 | 10-20 days | ฿16,947.00 |
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1,3-Dibromo-2-(bromomethyl)-5-fluorobenzene
This chemical is primarily utilized in organic synthesis as a versatile building block for the construction of complex molecules. Its multiple reactive sites, including bromine atoms and a fluorine substituent, make it valuable for cross-coupling reactions, such as Suzuki or Sonogashira couplings, which are essential in the development of pharmaceuticals and agrochemicals. The presence of the fluorine atom can enhance the biological activity and metabolic stability of the resulting compounds, making it particularly useful in drug discovery. Additionally, it serves as an intermediate in the production of specialty chemicals and materials, including polymers and liquid crystals, due to its ability to introduce specific functional groups into molecular frameworks.
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