3-Bromo-5-fluorobenzotrifluoride
98%
- Product Code: 118030
Alias:
5-fluoro-3-bromobenzotrifluoride; 3-bromo-α,α,α,5-tetrafluorotoluene; 1-bromo-3-fluoro-5-(trifluoromethyl)benzene
CAS:
130723-13-6
| Molecular Weight: | 243 g./mol | Molecular Formula: | BrC₆H₃FCF₃ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD00042498 | |
| Melting Point: | Boiling Point: | 138-139 °C(lit.) | |
| Density: | 1.511 g/mL at 25 °C(lit.) | Storage Condition: | room temperature |
Product Description:
3-Bromo-5-fluorobenzotrifluoride is widely used as a key intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its unique structure allows it to participate in various coupling reactions, such as Suzuki and Sonogashira reactions, which are essential for creating complex molecules. The compound is also employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce both fluorine and bromine substituents, which can enhance the biological activity and metabolic stability of drugs. Additionally, it serves as a building block in the synthesis of specialty chemicals and advanced materials, where its trifluoromethyl group imparts desirable properties like chemical resistance and thermal stability.
Product Specification:
| Test | Specification |
|---|---|
| Purity (GC) | 98 |
| Purity (Titration By Agno3 After Oxygen Combustion) | 97.5-102.5 |
| Purity (Titration By Agno3 After Oxygen Combustion) | 97.5-102.5 |
| Refractive Index N20/D | 1.453-1.457 |
| Relative Density (20/20) | 1.704-1.71 |
| Appearance | White To Off-White To Pale Yellow Solid Or Liquid |
| Infrared Spectrum | Conforms To Structure |
| Proton NMR Spectrum | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
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| 1.000 | 10-20 days | $12.04 |
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| 5.000 | 10-20 days | $24.09 |
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| 25.000 | 10-20 days | $54.82 |
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| 100.000 | 10-20 days | $206.40 |
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| 500.000 | 10-20 days | $997.94 |
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3-Bromo-5-fluorobenzotrifluoride
3-Bromo-5-fluorobenzotrifluoride is widely used as a key intermediate in organic synthesis, particularly in the pharmaceutical and agrochemical industries. Its unique structure allows it to participate in various coupling reactions, such as Suzuki and Sonogashira reactions, which are essential for creating complex molecules. The compound is also employed in the development of active pharmaceutical ingredients (APIs) due to its ability to introduce both fluorine and bromine substituents, which can enhance the biological activity and metabolic stability of drugs. Additionally, it serves as a building block in the synthesis of specialty chemicals and advanced materials, where its trifluoromethyl group imparts desirable properties like chemical resistance and thermal stability.
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