2,4-Dibromo-1,5-difluoro-3-nitrobenzene
≥95%
- Product Code: 40807
CAS:
144450-58-8
| Molecular Weight: | 316.88 g./mol | Molecular Formula: | C₆HBr₂F₂NO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD22681519 | |
| Melting Point: | Boiling Point: | 229.1±35.0°C at 760 mmHg | |
| Density: | Storage Condition: | Room temperature, dry and sealed |
Product Description:
This chemical is primarily utilized as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring bromine and fluorine substituents, makes it a valuable building block for creating molecules with specific electronic and steric properties. It is often employed in the development of active pharmaceutical ingredients (APIs) where the introduction of halogen atoms can enhance biological activity or stability. Additionally, it finds use in the preparation of specialty chemicals, including dyes and pigments, due to its ability to modify color properties and improve lightfastness. In research, it serves as a reagent in organic synthesis, particularly in cross-coupling reactions and nucleophilic aromatic substitution processes.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿1,600.00 |
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2,4-Dibromo-1,5-difluoro-3-nitrobenzene
This chemical is primarily utilized as an intermediate in the synthesis of more complex organic compounds, particularly in the pharmaceutical and agrochemical industries. Its structure, featuring bromine and fluorine substituents, makes it a valuable building block for creating molecules with specific electronic and steric properties. It is often employed in the development of active pharmaceutical ingredients (APIs) where the introduction of halogen atoms can enhance biological activity or stability. Additionally, it finds use in the preparation of specialty chemicals, including dyes and pigments, due to its ability to modify color properties and improve lightfastness. In research, it serves as a reagent in organic synthesis, particularly in cross-coupling reactions and nucleophilic aromatic substitution processes.
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