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CAS 500011-86-9

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3-bromo-1-(3-chloro-2-pyridinyl)-1H-Pyrazole-5-carboxylic acid

Description:
3-Bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid is a heterocyclic compound characterized by its pyrazole core, which is a five-membered ring containing two adjacent nitrogen atoms. The presence of a bromine atom at the 3-position and a chloro-substituent on a pyridine ring enhances its reactivity and potential biological activity. The carboxylic acid functional group at the 5-position contributes to its acidity and solubility in polar solvents. This compound is of interest in medicinal chemistry due to its potential applications in drug development, particularly in targeting specific biological pathways. Its structural features suggest it may exhibit diverse pharmacological properties, including anti-inflammatory or antimicrobial activities. The compound's molecular interactions can be influenced by the halogen substituents, which can affect its binding affinity to biological targets. Overall, 3-bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid represents a valuable scaffold for further research in the field of organic and medicinal chemistry.
Formula:C9H5BrClN3O2
InChI:InChI=1S/C9H5BrClN3O2/c10-7-4-6(9(15)16)14(13-7)8-5(11)2-1-3-12-8/h1-4H,(H,15,16)
InChI key:InChIKey=FORBXGROTPOMEH-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1N(N=C(Br)C1)C2=C(Cl)C=CC=N2
Synonyms:
  • 1H-Pyrazole-5-carboxylic acid, 3-bromo-1-(3-chloro-2-pyridinyl)
  • 3-bromo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid
  • 3-Bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid
  • 3-Bromo-1-(3-Chloro-2-Pyridinyl)-1H-Pyrazole
  • 3-BroMo-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxylic acid ISO 9001：2015 REACH
  • 3-Bromo-1-(3-chloropyridin-2-yl)
  • 3-Bromo-1-(3-chloro-2-pyridyl)pyrazole-5-carboxylic Acid
  • 5-Bromo-2-(3-chloro-2-pyridyl)pyrazole-3-carboxylic acid
  • 5-Bromo-2-(3-chloro-pyridin-2-yl)-2H-pyrazole-3-carboxylic acid
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