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CAS 50681-26-0

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6-Chloro-2,3-dihydro-3-oxo-4-pyridazinecarboxylic acid

Description:
6-Chloro-2,3-dihydro-3-oxo-4-pyridazinecarboxylic acid is a heterocyclic compound characterized by its pyridazine ring structure, which is a six-membered ring containing two nitrogen atoms. This compound features a chloro substituent at the 6-position and a carboxylic acid functional group, contributing to its acidic properties. The presence of the carbonyl group (oxo) at the 3-position enhances its reactivity, making it a potential candidate for various chemical reactions, including nucleophilic substitutions and condensation reactions. Its molecular structure suggests it may exhibit biological activity, which is often explored in medicinal chemistry. The compound is typically synthesized through specific organic reactions involving pyridazine derivatives. As with many heterocycles, it may exhibit unique solubility characteristics, often being soluble in polar solvents. Safety data should be consulted for handling, as the presence of chlorine can indicate potential toxicity or reactivity. Overall, 6-Chloro-2,3-dihydro-3-oxo-4-pyridazinecarboxylic acid is of interest in both synthetic and medicinal chemistry contexts.
Formula:C5H3ClN2O3
InChI:InChI=1S/C5H3ClN2O3/c6-3-1-2(5(10)11)4(9)8-7-3/h1H,(H,8,9)(H,10,11)
InChI key:InChIKey=LIXNWFSTAHULTE-UHFFFAOYSA-N
SMILES:C(O)(=O)C=1C(=O)NN=C(Cl)C1
Synonyms:
  • 4-Pyridazinecarboxylic Acid, 6-Chloro-2,3-Dihydro-3-Oxo-
  • 6-Chloro-2,3-dihydro-3-oxo-4-pyridazinecarboxylic acid
  • 6-Chloro-3-Hydroxypyridazine-4-Carboxylic Acid
  • NSC 338205
  • 6-Chloro-3-oxo-2,3-dihydropyridazine-4-carboxylic acid
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