2,5-Dibromo-1,3-difluorobenzene
≥98%
- Product Code: 115411
CAS:
128259-71-2
| Molecular Weight: | 271.89 g./mol | Molecular Formula: | C₆H₂Br₂F₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD07783665 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C |
Product Description:
2,5-Dibromo-1,3-difluorobenzene is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique combination of bromine and fluorine atoms makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and advanced materials. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic rings with specific halogen substitutions into target molecules. This is especially useful in drug discovery, where the introduction of fluorine atoms can enhance the biological activity, metabolic stability, and bioavailability of potential drug candidates. Additionally, it serves as a precursor in the synthesis of liquid crystals and polymers, where the presence of halogens can influence the material's electronic properties and thermal stability. Its role in the production of specialty chemicals and functional materials underscores its importance in industrial and research applications.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | Solid-liquid Mixture |
| Purity (%) | 97.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.200 | 10-20 days | $16.07 |
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| 1.000 | 10-20 days | $26.62 |
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| 5.000 | 10-20 days | $99.45 |
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2,5-Dibromo-1,3-difluorobenzene
2,5-Dibromo-1,3-difluorobenzene is primarily utilized in the field of organic synthesis as a versatile building block for the development of more complex chemical structures. Its unique combination of bromine and fluorine atoms makes it particularly valuable in the creation of pharmaceuticals, agrochemicals, and advanced materials. The compound is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to introduce aromatic rings with specific halogen substitutions into target molecules. This is especially useful in drug discovery, where the introduction of fluorine atoms can enhance the biological activity, metabolic stability, and bioavailability of potential drug candidates. Additionally, it serves as a precursor in the synthesis of liquid crystals and polymers, where the presence of halogens can influence the material's electronic properties and thermal stability. Its role in the production of specialty chemicals and functional materials underscores its importance in industrial and research applications.
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