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CAS 46413-66-5

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3-(4-bromophenyl)-1H-pyrazole-5-carboxylic acid

Description:
3-(4-Bromophenyl)-1H-pyrazole-5-carboxylic acid is an organic compound characterized by its pyrazole ring structure, which is a five-membered ring containing two adjacent nitrogen atoms. The presence of a carboxylic acid functional group (-COOH) at the 5-position of the pyrazole contributes to its acidity and reactivity, making it useful in various chemical reactions. The 4-bromophenyl substituent at the 3-position enhances its lipophilicity and can influence its biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its molecular structure allows for potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as pyrazole derivatives are known for their diverse biological activities, including anti-inflammatory and analgesic properties. Additionally, the bromine atom can serve as a useful handle for further chemical modifications, making this compound a valuable intermediate in synthetic organic chemistry.
Formula:C10H7BrN2O2
InChI:InChI=1/C10H7BrN2O2/c11-7-3-1-6(2-4-7)8-5-9(10(14)15)13-12-8/h1-5H,(H,12,13)(H,14,15)
SMILES:c1cc(ccc1c1cc(C(=O)O)n[nH]1)Br
Synonyms:
  • 1H-pyrazole-3-carboxylic acid, 5-(4-bromophenyl)-
  • 1H-pyrazole-5-carboxylic acid, 3-(4-bromophenyl)-
  • 5-(4-Bromophenyl)-1H-pyrazole-3-carboxylic acid
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