Description

2-Bromoheptafluoronaphthalene (CAS No. 27041-17-4) is a highly fluorinated aromatic compound with the molecular formula C₁₀BrF₇. This specialized chemical is characterized by its naphthalene backbone substituted with seven fluorine atoms and one bromine atom, offering unique reactivity and stability for advanced synthetic applications. With an IUPAC name of 2-bromo-1,3,4,5,6,7,8-heptafluoronaphthalene, it is a valuable intermediate in organofluorine chemistry, particularly for constructing complex fluorinated architectures. Its high purity and well-defined structure make it ideal for researchers developing pharmaceuticals, agrochemicals, or materials requiring tailored fluorination. Available in rigorously controlled batches, this compound is supplied with comprehensive analytical data (GC/MS, NMR) to ensure reproducibility in demanding research environments.

Properties

• CAS Number: 27041-17-4
• Complexity: 317
• IUPAC Name: 2-bromo-1,3,4,5,6,7,8-heptafluoro-naphthalene
• InChI: InChI=1S/C10BrF7/c11-3-4(12)1-2(5(13)8(3)16)7(15)10(18)9(17)6(1)14
• InChI Key: PMTDLHCXDWASRN-UHFFFAOYSA-N
• Exact Mass: 331.90716
• Molecular Formula: C10BrF7
• Molecular Weight: 333.00
• SMILES: C12=C(C(=C(C(=C1F)F)F)F)C(=C(C(=C2F)F)Br)F
• Monoisotopic Mass: 331.90716
• Synonyms: 2-Bromoheptafluoronaphthalene, 27041-17-4, DTXSID30465603, DTXCID20416422, 2-bromo-1,3,4,5,6,7,8-heptafluoronaphthalene, 2-BROMOPERFLUORONAPHTHALENE, MFCD07784218, 2-bromoheptafluoro-naphthalene, SCHEMBL3020625, AKOS016007807, FB88327, AC-25496, DB-025256, G66699

Application

2-Bromoheptafluoronaphthalene serves as a key building block in the synthesis of fluorinated organic materials, particularly for electronic and pharmaceutical applications where enhanced stability and lipophilicity are required. Its electron-deficient aromatic system makes it valuable in cross-coupling reactions to create novel fluorinated ligands or polymers. Researchers utilize this compound to develop advanced liquid crystals and corrosion-resistant coatings due to its thermal and chemical inertness. In medicinal chemistry, it acts as a precursor for PET radiotracer development by leveraging its facile bromine substitution chemistry.

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