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Atomfair 1-Bromo-2,3,4,5-tetrafluorobenzene C6HBrF4
Description 1-Bromo-2,3,4,5-tetrafluorobenzene (CAS No. 1074-91-5) is a high-purity fluorinated aromatic compound with the molecular formula C6HBrF4. This organobromine derivative is characterized by its tetrafluorinated benzene ring, making it a valuable intermediate in synthetic organic chemistry and materials science. Its unique structure offers excellent reactivity for nucleophilic substitutions, cross-coupling reactions, and as a precursor for advanced fluorinated materials. Suitable for research and industrial applications, this compound is supplied with rigorous quality control to ensure consistency in performance. Store in a cool, dry place away from light and moisture to maintain stability.
Description
Description
1-Bromo-2,3,4,5-tetrafluorobenzene (CAS No. 1074-91-5) is a high-purity fluorinated aromatic compound with the molecular formula C6HBrF4. This organobromine derivative is characterized by its tetrafluorinated benzene ring, making it a valuable intermediate in synthetic organic chemistry and materials science. Its unique structure offers excellent reactivity for nucleophilic substitutions, cross-coupling reactions, and as a precursor for advanced fluorinated materials. Suitable for research and industrial applications, this compound is supplied with rigorous quality control to ensure consistency in performance. Store in a cool, dry place away from light and moisture to maintain stability.
- CAS No: 1074-91-5
- Molecular Formula: C6HBrF4
- Molecular Weight: 228.97
- Exact Mass: 227.91978
- Monoisotopic Mass: 227.91978
- IUPAC Name: 1-bromo-2,3,4,5-tetrafluorobenzene
- SMILES: C1=C(C(=C(C(=C1Br)F)F)F)F
- Synonyms: 1-Bromo-2,3,4,5-tetrafluorobenzene, 1074-91-5, EINECS 214-048-7, DTXSID50148042, DTXCID9070533
Application
1-Bromo-2,3,4,5-tetrafluorobenzene is widely used as a key building block in the synthesis of pharmaceuticals, agrochemicals, and liquid crystals. Its electron-deficient aromatic ring makes it ideal for Suzuki-Miyaura and other cross-coupling reactions. Researchers also employ it in the development of fluorinated polymers and advanced materials with enhanced thermal and chemical resistance. Additionally, it serves as a precursor for ligands and catalysts in organometallic chemistry.
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