3-Bromo-4-fluorotoluene
99%
- Product Code: 117993
Alias:
3-Bromo-4-fluorotoluene
CAS:
452-62-0
| Molecular Weight: | 189.02 g./mol | Molecular Formula: | C₇H₆BrF |
|---|---|---|---|
| EC Number: | 207-201-4 | MDL Number: | MFCD00040827 |
| Melting Point: | Boiling Point: | 169 °C756 mm Hg(lit.) | |
| Density: | 1.507 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
3-Bromo-4-fluorotoluene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of complex molecules. In pharmaceutical research, it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs) that may exhibit therapeutic properties. Additionally, it is employed in the creation of specialty chemicals and dyes, where its halogenated aromatic ring contributes to desired chemical properties. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, is also notable, enabling the formation of carbon-carbon or carbon-heteroatom bonds in advanced synthetic processes.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 99 |
| Refractive Index N20/D | 1.529-1.532 |
| Specific Gravity (20/20) | 1.518-1.522 |
| Appearance | Light Yellow Liquid |
| Infrared Spectrometry | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | $15.78 |
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| 25.000 | 10-20 days | $52.33 |
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| 100.000 | 10-20 days | $171.51 |
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| 500.000 | 10-20 days | $676.51 |
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3-Bromo-4-fluorotoluene
3-Bromo-4-fluorotoluene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its structure allows for further functionalization, making it valuable in the development of complex molecules. In pharmaceutical research, it serves as a building block for the synthesis of active pharmaceutical ingredients (APIs) that may exhibit therapeutic properties. Additionally, it is employed in the creation of specialty chemicals and dyes, where its halogenated aromatic ring contributes to desired chemical properties. Its role in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, is also notable, enabling the formation of carbon-carbon or carbon-heteroatom bonds in advanced synthetic processes.
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