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CAS 618383-44-1

:

5-(4-fluorophenyl)-1H-pyrazole-4-carboxylic acid

Description:
5-(4-Fluorophenyl)-1H-pyrazole-4-carboxylic acid is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. The presence of a carboxylic acid functional group (-COOH) at the 4-position of the pyrazole contributes to its acidity and reactivity, making it a potential candidate for various chemical reactions. The 4-fluorophenyl substituent at the 5-position enhances its lipophilicity and may influence its biological activity. This compound is typically used in medicinal chemistry and research, particularly in the development of pharmaceuticals due to its potential as a bioactive molecule. Its properties, such as solubility, melting point, and stability, can vary based on the specific conditions and solvents used. Additionally, the fluorine atom can impart unique electronic properties, affecting the compound's interaction with biological targets. Overall, 5-(4-fluorophenyl)-1H-pyrazole-4-carboxylic acid is a versatile compound with applications in drug discovery and development.
Formula:C10H7FN2O2
InChI:InChI=1/C10H7FN2O2/c11-7-3-1-6(2-4-7)9-8(10(14)15)5-12-13-9/h1-5H,(H,12,13)(H,14,15)
SMILES:c1cc(ccc1c1c(c[nH]n1)C(=O)O)F
Synonyms:
  • 1H-pyrazole-4-carboxylic acid, 3-(4-fluorophenyl)-
  • 3-(4-fluorophenyl)-1H-pyrazole-4-carboxylic acid
  • 5-(4-Fluorophenyl)-1H-pyrazole-4-carboxylic acid
  • AKOS PAO-0309
  • RARECHEM AL BE 1274
  • SALOR-INT L324558-1EA
  • 1H-Pyrazole-4-carboxylicacid, 3-(4-fluorophenyl)-
  • 3-(4-fluorophenyl)-2H-pyrazole-4-carboxylic acid
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