2-Bromo-1-fluoro-4-nitrobenzene
99.5%
- Product Code: 116627
CAS:
701-45-1
| Molecular Weight: | 220 g./mol | Molecular Formula: | C₆H₃BrFNO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00055433 | |
| Melting Point: | 55°C | Boiling Point: | |
| Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring bromo, fluoro, and nitro groups, makes it a versatile building block for constructing more complex molecules. It is often employed in nucleophilic aromatic substitution reactions, where the bromo and fluoro groups can be selectively replaced by other functional groups. Additionally, it serves as a precursor in the synthesis of dyes, pigments, and other specialty chemicals. Its nitro group also makes it useful in reactions involving reduction to form amines, which are key intermediates in drug development.
Product Specification:
| Test | Specification |
|---|---|
| Melting Point (Degree Celsius) | 55-59 |
| Purity (%) | 99.5-100 |
| Appearance | White To Grey Powder Or Crystals |
| Infrared Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿640.00 |
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| 5.000 | 10-20 days | ฿1,780.00 |
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| 25.000 | 10-20 days | ฿7,680.00 |
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2-Bromo-1-fluoro-4-nitrobenzene
This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure, featuring bromo, fluoro, and nitro groups, makes it a versatile building block for constructing more complex molecules. It is often employed in nucleophilic aromatic substitution reactions, where the bromo and fluoro groups can be selectively replaced by other functional groups. Additionally, it serves as a precursor in the synthesis of dyes, pigments, and other specialty chemicals. Its nitro group also makes it useful in reactions involving reduction to form amines, which are key intermediates in drug development.
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