3-Aminopyridazine-4-carboxylic acid is an organic compound characterized by its pyridazine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms. The compound features an amino group (-NH2) at the 3-position and a carboxylic acid group (-COOH) at the 4-position of the pyridazine ring, contributing to its acidic properties. This structure imparts both basic and acidic functionalities, making it a versatile compound in various chemical reactions. It is typically a white to off-white crystalline solid, soluble in water and polar organic solvents due to the presence of the carboxylic acid group. The compound is of interest in pharmaceutical and agrochemical research, as it may exhibit biological activity or serve as a building block for the synthesis of more complex molecules. Its CAS number, 21141-03-7, is a unique identifier that facilitates the search for information regarding its properties, safety, and applications in scientific literature and databases.

3-aminopyridazine-4-carboxylic acid

21141-03-7: 4-Pyridazinecarboxylic acid, 3-amino-, 3-Amino-4-Pyridazinecarboxylic Acid, 3-Aminopyridazine-4-carboxylic acid

3-Amino-4-pyridazinecarboxylic acid

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CAS 21141-03-7: 3-aminopyridazine-4-carboxylic acid

3-Amino-4-pyridazinecarboxylic acid

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3-Amino-4-pyridazinecarboxylic acid

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4-Pyridazinecarboxylic acid, 3-amino-

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3-Aminopyridazine-4-carboxylic acid

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