4-Bromo-2-fluorotoluene
98%
- Product Code: 119283
Alias:
4-Bromo-2-fluorotoluene 2-fluoro-4-bromotoluene
CAS:
51436-99-8
| Molecular Weight: | 189.02 g./mol | Molecular Formula: | C₇H₆BrF |
|---|---|---|---|
| EC Number: | 257-201-3 | MDL Number: | MFCD00013551 |
| Melting Point: | Boiling Point: | 68 °C (8 mmHg) | |
| Density: | 1.492 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
4-Bromo-2-fluorotoluene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure, combining bromine and fluorine substituents on a toluene backbone, makes it valuable for constructing complex molecules. In the pharmaceutical industry, it serves as a building block for developing active pharmaceutical ingredients (APIs) with specific biological activities. Additionally, it is utilized in the synthesis of specialty chemicals, including dyes and pigments, due to its ability to introduce halogenated aromatic groups into target compounds. Its role in cross-coupling reactions, such as Suzuki and Heck reactions, further highlights its importance in advanced chemical manufacturing.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 97.5-100 |
| Refractive Index N20/D | 1.526-1.53 |
| Specific Gravity (20/20) | 1.507-1.512 |
| Appearance | Colorless To Yellow Liquid |
| Infrared Spectrum | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 5.000 | 10-20 days | ฿300.00 |
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| 25.000 | 10-20 days | ฿550.00 |
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| 100.000 | 10-20 days | ฿1,880.00 |
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4-Bromo-2-fluorotoluene
4-Bromo-2-fluorotoluene is primarily used as an intermediate in organic synthesis, particularly in the production of pharmaceuticals and agrochemicals. Its unique structure, combining bromine and fluorine substituents on a toluene backbone, makes it valuable for constructing complex molecules. In the pharmaceutical industry, it serves as a building block for developing active pharmaceutical ingredients (APIs) with specific biological activities. Additionally, it is utilized in the synthesis of specialty chemicals, including dyes and pigments, due to its ability to introduce halogenated aromatic groups into target compounds. Its role in cross-coupling reactions, such as Suzuki and Heck reactions, further highlights its importance in advanced chemical manufacturing.
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