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Atomfair Cinchophen C16H11NO2

Description Cinchophen (CAS 132-60-5), also known as 2-phenylquinoline-4-carboxylic acid, is a quinoline derivative with the molecular formula C16H11NO2. This high-purity compound is a valuable research chemical, commonly utilized in biochemical and pharmacological studies. Its crystalline structure and well-defined properties make it ideal for analytical applications, including HPLC, LC-MS, and spectroscopy. Cinchophen is supplied as a fine powder with ??98% purity, ensuring consistency for laboratory use. Proper storage in a cool, dry environment is recommended to maintain stability. Suitable for researchers investigating anti-inflammatory, analgesic, or uricosuric mechanisms.

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Description

Description

Cinchophen (CAS 132-60-5), also known as 2-phenylquinoline-4-carboxylic acid, is a quinoline derivative with the molecular formula C16H11NO2. This high-purity compound is a valuable research chemical, commonly utilized in biochemical and pharmacological studies. Its crystalline structure and well-defined properties make it ideal for analytical applications, including HPLC, LC-MS, and spectroscopy. Cinchophen is supplied as a fine powder with ??98% purity, ensuring consistency for laboratory use. Proper storage in a cool, dry environment is recommended to maintain stability. Suitable for researchers investigating anti-inflammatory, analgesic, or uricosuric mechanisms.

  • CAS No: 132-60-5
  • Molecular Formula: C16H11NO2
  • Molecular Weight: 249.26
  • Exact Mass: 249.078978594
  • Monoisotopic Mass: 249.078978594
  • IUPAC Name: 2-phenylquinoline-4-carboxylic acid
  • SMILES: C1=CC=C(C=C1)C2=NC3=CC=CC=C3C(=C2)C(=O)O
  • Synonyms: Cinchophen, 2-Phenylquinoline-4-carboxylic acid, 2-Phenyl-4-quinolinecarboxylic acid, Cinchopen, 2-Phenylcinchoninic acid

Application

Cinchophen has been historically studied for its uricosuric and anti-inflammatory properties, making it relevant for research on gout and metabolic disorders. It serves as a model compound in pharmacological studies exploring quinoline derivatives. Researchers also investigate its potential interactions with proteins and enzymes in biochemical pathways. Its structural features make it useful as a building block in synthetic organic chemistry.

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