3-Chloro-6-methyl-pyridazine-4-carboxylic acid is a heterocyclic organic compound characterized by its pyridazine ring structure, which contains both nitrogen and carbon atoms. The presence of a carboxylic acid functional group (-COOH) indicates that it can act as an acid, contributing to its reactivity and solubility in polar solvents. The chlorine substituent at the 3-position and the methyl group at the 6-position of the pyridazine ring influence its chemical properties, including its potential for electrophilic substitution reactions. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure allows for various interactions, such as hydrogen bonding, which can affect its solubility and stability. Additionally, the presence of the carboxylic acid group suggests that it can participate in acid-base reactions. Overall, 3-chloro-6-methyl-pyridazine-4-carboxylic acid is a versatile compound with potential applications in organic synthesis and medicinal chemistry.

3-chloro-6-methyl-pyridazine-4-carboxylic acid

914637-40-4: 3-Chloro-6-methylpyridazine-4-carboxylic acid, 4-Pyridazinecarboxylic acid, 3-chloro-6-methyl-

3-Chloro-6-methylpyridazine-4-carboxylic acid

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CAS 914637-40-4: 3-chloro-6-methyl-pyridazine-4-carboxylic acid

3-Chloro-6-methylpyridazine-4-carboxylic acid

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3-Chloro-6-methylpyridazine-4-carboxylic acid

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3-Chloro-6-methylpyridazine-4-carboxylic acid

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3-Chloro-6-methylpyridazine-4-carboxylic acid

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