3-Bromo-5-fluorobenzotrifluoride
98%
Reagent
Code: #118030
Alias
5-fluoro-3-bromobenzotrifluoride; 3-bromo-α,α,α,5-tetrafluorotoluene; 1-bromo-3-fluoro-5-(trifluoromethyl)benzene
CAS Number
130723-13-6
blur_circular Chemical Specifications
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Molecular Information
Weight
243 g/mol
Formula
BrC₆H₃FCF₃
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Registry Numbers
MDL Number
MFCD00042498
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Physical Properties
Boiling Point
138-139 °C(lit.)
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Storage & Handling
Density
1.511 g/mL at 25 °C(lit.)
Storage
room temperature
description 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.
format_list_bulleted Product Specification
| Test Parameter | 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 |
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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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