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Atomfair 2,8-Dibromodibenzothiophene C12H6Br2S

Description 2,8-Dibromodibenzothiophene (CAS No. 31574-87-5) is a high-purity brominated dibenzothiophene derivative with the molecular formula C12H6Br2S . This heterocyclic aromatic compound is widely utilized in organic synthesis, materials science, and pharmaceutical research due to its unique electronic and steric properties. The dibromination at the 2,8-positions enhances its reactivity as a building block for Suzuki coupling, Buchwald-Hartwig amination, and other cross-coupling reactions. Our product is rigorously tested via HPLC, GC-MS, and1H/13C NMR to ensure ??98% purity, meeting the stringent requirements of advanced research applications. Supplied as a crystalline solid with documented lot-specific analytical data, it is ideal for developing organic semiconductors,…

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Description

Description

2,8-Dibromodibenzothiophene (CAS No. 31574-87-5) is a high-purity brominated dibenzothiophene derivative with the molecular formula C12H6Br2S. This heterocyclic aromatic compound is widely utilized in organic synthesis, materials science, and pharmaceutical research due to its unique electronic and steric properties. The dibromination at the 2,8-positions enhances its reactivity as a building block for Suzuki coupling, Buchwald-Hartwig amination, and other cross-coupling reactions. Our product is rigorously tested via HPLC, GC-MS, and 1H/13C NMR to ensure ??98% purity, meeting the stringent requirements of advanced research applications. Supplied as a crystalline solid with documented lot-specific analytical data, it is ideal for developing organic semiconductors, ligands, or bioactive molecules.

  • CAS No: 31574-87-5
  • Molecular Formula: C12H6Br2S
  • Molecular Weight: 342.05
  • Exact Mass: 341.85365
  • Monoisotopic Mass: 339.85570
  • IUPAC Name: 2,8-dibromodibenzothiophene
  • SMILES: C1=CC2=C(C=C1Br)C3=C(S2)C=CC(=C3)Br
  • Synonyms: 2,8-Dibromodibenzothiophene, 31574-87-5, DTXSID40348155, DTXCID70299227, 636-527-3

Application

2,8-Dibromodibenzothiophene serves as a key precursor in synthesizing ??-conjugated systems for organic electronics, including OLEDs and OFETs, due to its planar structure and bromine-mediated reactivity. Researchers employ it to construct thiophene-based ligands for transition-metal catalysts in asymmetric synthesis. In medicinal chemistry, it acts as a scaffold for developing kinase inhibitors or antimicrobial agents by functionalizing the dibenzothiophene core.

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