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Atomfair 3-Bromo-5-fluorobenzotrifluoride C7H3BrF4
Description 3-Bromo-5-fluorobenzotrifluoride (CAS No. 130723-13-6) is a high-purity halogenated aromatic compound with the molecular formula C7H3BrF4. This specialized chemical, also known by its IUPAC name 1-bromo-3-fluoro-5-(trifluoromethyl)benzene , features a benzene ring substituted with bromine, fluorine, and a trifluoromethyl group, making it a valuable building block in synthetic organic chemistry. Its unique structure offers excellent reactivity for cross-coupling reactions, nucleophilic substitutions, and other transformations. Ideal for pharmaceutical, agrochemical, and materials science research, this compound is supplied with comprehensive analytical data (GC/HPLC, NMR) to ensure quality and consistency. Store in a cool, dry place under inert atmosphere to maintain stability.
Description
Description
3-Bromo-5-fluorobenzotrifluoride (CAS No. 130723-13-6) is a high-purity halogenated aromatic compound with the molecular formula C7H3BrF4. This specialized chemical, also known by its IUPAC name 1-bromo-3-fluoro-5-(trifluoromethyl)benzene, features a benzene ring substituted with bromine, fluorine, and a trifluoromethyl group, making it a valuable building block in synthetic organic chemistry. Its unique structure offers excellent reactivity for cross-coupling reactions, nucleophilic substitutions, and other transformations. Ideal for pharmaceutical, agrochemical, and materials science research, this compound is supplied with comprehensive analytical data (GC/HPLC, NMR) to ensure quality and consistency. Store in a cool, dry place under inert atmosphere to maintain stability.
- CAS No: 130723-13-6
- Molecular Formula: C7H3BrF4
- Molecular Weight: 243.00
- Exact Mass: 241.93543
- Monoisotopic Mass: 241.93543
- IUPAC Name: 1-bromo-3-fluoro-5-(trifluoromethyl)benzene
- SMILES: C1=C(C=C(C=C1F)Br)C(F)(F)F
- Synonyms: 3-Bromo-5-fluorobenzotrifluoride, 130723-13-6, DTXSID50371277, DTXCID60322311, 642-494-6
Application
3-Bromo-5-fluorobenzotrifluoride is widely used as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its electron-deficient aromatic ring makes it suitable for Suzuki, Stille, and other palladium-catalyzed cross-coupling reactions. Researchers also employ it to introduce trifluoromethyl groups into target molecules, enhancing metabolic stability and lipophilicity. In material science, it serves as a precursor for liquid crystals and organic electronic components.
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