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Atomfair Ethanone, 1,1′-[1,1′-biphenyl]-4,4′-diylbis[2-bromo- C16H12Br2O2

Description Ethanone, 1,1′-[1,1′-biphenyl]-4,4′-diylbis[2-bromo- (CAS No. 4072-67-7) is a high-purity organic compound with the molecular formula C16H12Br2O2. This crystalline solid is a bifunctional brominated ketone derivative, characterized by its biphenyl core symmetrically substituted with 2-bromoacetyl groups. As a versatile building block in organic synthesis, it offers exceptional reactivity for nucleophilic substitution and cross-coupling reactions. Our product undergoes rigorous quality control to ensure ??98% purity (HPLC) with detailed characterization including1H/13C NMR and mass spectrometry data. Suitable for pharmaceutical intermediates, materials science research, and as a precursor for conjugated polymers. Packaged under inert atmosphere in amber glass vials to ensure stability.

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Description

Description

Ethanone, 1,1′-[1,1′-biphenyl]-4,4′-diylbis[2-bromo- (CAS No. 4072-67-7) is a high-purity organic compound with the molecular formula C16H12Br2O2. This crystalline solid is a bifunctional brominated ketone derivative, characterized by its biphenyl core symmetrically substituted with 2-bromoacetyl groups. As a versatile building block in organic synthesis, it offers exceptional reactivity for nucleophilic substitution and cross-coupling reactions. Our product undergoes rigorous quality control to ensure ??98% purity (HPLC) with detailed characterization including 1H/13C NMR and mass spectrometry data. Suitable for pharmaceutical intermediates, materials science research, and as a precursor for conjugated polymers. Packaged under inert atmosphere in amber glass vials to ensure stability.

  • CAS No: 4072-67-7
  • Molecular Formula: C16H12Br2O2
  • Molecular Weight: 396.07
  • Exact Mass: 395.91836
  • Monoisotopic Mass: 393.92040
  • IUPAC Name: 2-bromo-1-[4-[4-(2-bromoacetyl)phenyl]phenyl]ethanone
  • SMILES: C1=CC(=CC=C1C2=CC=C(C=C2)C(=O)CBr)C(=O)CBr
  • Synonyms: 4,4′-Bis(2-bromoacetyl)biphenyl, EINECS 223-785-3, Ethanone, 1,1′-[1,1′-biphenyl]-4,4′-diylbis[2-bromo-, DTXSID0063286, 1,1′-[1,1′-biphenyl]-4,4′-diylbis[2-bromoethan-1-one]

Application

This compound serves as a key intermediate in the synthesis of organic electronic materials, particularly for creating conjugated systems in OLED and OPV applications. Researchers utilize its reactive bromoacetyl groups for efficient cross-coupling in polymer synthesis. The symmetrical bifunctional nature makes it valuable for creating rigid-rod polymers and molecular scaffolds. In medicinal chemistry, it finds use as a precursor for kinase inhibitor development.

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