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CAS 21579-37-3

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5-aminopyridazine-4-carboxylic acid

Description:
5-Aminopyridazine-4-carboxylic acid is an organic compound characterized by its pyridazine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 2. This compound features an amino group (-NH2) at the 5-position and a carboxylic acid group (-COOH) at the 4-position of the pyridazine ring, contributing to its acidic properties. It is typically a white to off-white solid and is soluble in polar solvents due to the presence of the carboxylic acid group. The compound is of interest in various fields, including medicinal chemistry and agrochemicals, due to its potential biological activities. Its structure allows for various chemical modifications, making it a versatile building block in synthetic chemistry. Additionally, the presence of both amino and carboxylic acid functional groups can facilitate hydrogen bonding, influencing its reactivity and interactions in biological systems. Overall, 5-aminopyridazine-4-carboxylic acid is a significant compound with diverse applications in research and industry.
Formula:C5H5N3O2
InChI:InChI=1/C5H5N3O2/c6-4-2-8-7-1-3(4)5(9)10/h1-2H,(H2,6,7)(H,9,10)
SMILES:c1c(c(cnn1)N)C(=O)O
Synonyms:
  • 4-Pyridazinecarboxylic Acid, 5-Amino-
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