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Atomfair 1-bromo-9,9-dimethyl-9H-fluorene C15H13Br

Description 1-Bromo-9,9-dimethyl-9H-fluorene (CAS No. 1225053-54-2) is a high-purity brominated fluorene derivative with the molecular formula C15H13Br. This compound features a unique 9,9-dimethylfluorene backbone with a bromine substituent at the 1-position, offering exceptional reactivity for cross-coupling reactions, such as Suzuki-Miyaura and Negishi couplings. Its rigid, planar structure makes it an ideal building block for organic semiconductors, OLED materials, and advanced polymer synthesis. With a molecular weight of 273.17 g/mol, this reagent is supplied as a crystalline solid with >95% purity (HPLC), ensuring consistent performance in research and industrial applications. Proper storage under inert conditions is recommended to maintain stability.

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Description

Description

1-Bromo-9,9-dimethyl-9H-fluorene (CAS No. 1225053-54-2) is a high-purity brominated fluorene derivative with the molecular formula C15H13Br. This compound features a unique 9,9-dimethylfluorene backbone with a bromine substituent at the 1-position, offering exceptional reactivity for cross-coupling reactions, such as Suzuki-Miyaura and Negishi couplings. Its rigid, planar structure makes it an ideal building block for organic semiconductors, OLED materials, and advanced polymer synthesis. With a molecular weight of 273.17 g/mol, this reagent is supplied as a crystalline solid with >95% purity (HPLC), ensuring consistent performance in research and industrial applications. Proper storage under inert conditions is recommended to maintain stability.

  • CAS No: 1225053-54-2
  • Molecular Formula: C15H13Br
  • Molecular Weight: 273.17
  • Exact Mass: 272.02006
  • Monoisotopic Mass: 272.02006
  • IUPAC Name: 1-bromo-9,9-dimethylfluorene
  • SMILES: CC1(C2=CC=CC=C2C3=C1C(=CC=C3)Br)C
  • Synonyms: 1-bromo-9,9-dimethyl-9H-fluorene, 1225053-54-2, 9H-Fluorene, 1-bromo-9,9-dimethyl-, 1-bromo-9,9-dimethylfluorene, starbld0001382

Application

1-Bromo-9,9-dimethyl-9H-fluorene is widely used in materials science as a key intermediate for synthesizing ??-conjugated polymers and small molecules for optoelectronic devices. Its bromine moiety enables efficient palladium-catalyzed coupling reactions to construct extended aromatic systems for organic light-emitting diodes (OLEDs) and photovoltaic materials. Researchers also employ it to modify fluorene-based scaffolds in supramolecular chemistry and liquid crystal development.

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