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Atomfair 3-Bromodibenzofuran C12H7BrO

Description 3-Bromodibenzofuran (CAS No. 26608-06-0) is a high-purity brominated dibenzofuran derivative with the molecular formula C12H7BrO . This heterocyclic aromatic compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its versatile reactivity as a halogenated building block. The product is supplied as a crystalline solid with guaranteed ??95% purity (HPLC), rigorously tested for consistency via GC-MS and NMR spectroscopy. Optimal storage conditions recommend protection from light at 2-8??C in sealed containers under inert atmosphere to prevent degradation. Ideal for Suzuki couplings, cross-coupling reactions, and as a precursor for advanced OLED materials. CAS: 26608-06-0 Molecular Weight:…

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Description

Description

3-Bromodibenzofuran (CAS No. 26608-06-0) is a high-purity brominated dibenzofuran derivative with the molecular formula C12H7BrO. This heterocyclic aromatic compound is widely utilized in organic synthesis, pharmaceutical research, and material science due to its versatile reactivity as a halogenated building block. The product is supplied as a crystalline solid with guaranteed ??95% purity (HPLC), rigorously tested for consistency via GC-MS and NMR spectroscopy. Optimal storage conditions recommend protection from light at 2-8??C in sealed containers under inert atmosphere to prevent degradation. Ideal for Suzuki couplings, cross-coupling reactions, and as a precursor for advanced OLED materials.

  • CAS: 26608-06-0
  • Molecular Weight: 247.09 g/mol
  • Melting Point: 82-86??C
  • Hazard Codes: Xi (Irritant)
  • CAS No: 26608-06-0
  • Molecular Formula: C12H7BrO
  • Molecular Weight: 247.09
  • Exact Mass: 245.96803
  • Monoisotopic Mass: 245.96803
  • IUPAC Name: 3-bromodibenzofuran
  • SMILES: C1=CC=C2C(=C1)C3=C(O2)C=C(C=C3)Br
  • Synonyms: 3-bromodibenzofuran, 987-842-0, 3-bromodibenzo[b,d]furan, 26608-06-0, Dibenzofuran, 3-bromo-

Application

3-Bromodibenzofuran serves as a critical intermediate in the synthesis of polycyclic aromatic hydrocarbons (PAHs) for optoelectronic materials. Researchers employ this compound in palladium-catalyzed cross-coupling reactions to construct complex conjugated systems for organic semiconductors. In pharmaceutical development, it functions as a scaffold for kinase inhibitor candidates targeting inflammatory pathways. The bromine moiety enables further functionalization via nucleophilic substitution or metal-halogen exchange reactions.

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