Atomfair 9-oxo-9H-fluorenecarboxylic acid C14H8O3

Description 9-Oxo-9H-fluorenecarboxylic acid (CAS No. 16002-29-2) is a high-purity organic compound with the molecular formula C14H8O3and IUPAC name 9-oxofluorene-1-carboxylic acid . This fine chemical is characterized by its fluorene backbone functionalized with a carboxylic acid group at the 1-position and a ketone at the 9-position, making it a versatile intermediate in synthetic organic chemistry. It is supplied as a crystalline solid with >95% purity (HPLC), ensuring consistency for research and industrial applications. Suitable for use in pharmaceuticals, materials science, and as a building block for advanced organic synthesis. Store in a cool, dry place, protected from light and moisture to…

Description

Description

9-Oxo-9H-fluorenecarboxylic acid (CAS No. 16002-29-2) is a high-purity organic compound with the molecular formula C14H8O3 and IUPAC name 9-oxofluorene-1-carboxylic acid. This fine chemical is characterized by its fluorene backbone functionalized with a carboxylic acid group at the 1-position and a ketone at the 9-position, making it a versatile intermediate in synthetic organic chemistry. It is supplied as a crystalline solid with >95% purity (HPLC), ensuring consistency for research and industrial applications. Suitable for use in pharmaceuticals, materials science, and as a building block for advanced organic synthesis. Store in a cool, dry place, protected from light and moisture to maintain stability.

  • CAS No: 16002-29-2
  • Molecular Formula: C14H8O3
  • Molecular Weight: 224.21
  • Exact Mass: 224.047344113
  • Monoisotopic Mass: 224.047344113
  • IUPAC Name: 9-oxofluorene-1-carboxylic acid
  • SMILES: C1=CC=C2C(=C1)C3=C(C2=O)C(=CC=C3)C(=O)O
  • Synonyms: 9-Oxo-9H-fluorenecarboxylic acid, EINECS 216-396-5, DTXSID30166244, NSC 24049, DTXCID2088735

Application

9-Oxo-9H-fluorenecarboxylic acid is widely utilized as a key intermediate in the synthesis of fluorene-based derivatives for optoelectronic materials and pharmaceutical research. Its reactive carboxylic acid group enables facile conjugation or further functionalization, making it valuable in polymer chemistry and small-molecule drug development. Researchers also employ it in the study of charge-transfer complexes due to its conjugated aromatic system.

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