Methyl 6-methoxypyridazine-3-carboxylate, identified by its CAS number 19194-96-8, is an organic compound characterized by its pyridazine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms. This compound features a methoxy group (-OCH3) at the 6-position and a carboxylate ester group (-COOCH3) at the 3-position, contributing to its chemical reactivity and potential applications. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the methoxy group enhances its solubility in organic solvents, while the carboxylate moiety can participate in various chemical reactions, such as esterification and nucleophilic substitutions. Methyl 6-methoxypyridazine-3-carboxylate may exhibit biological activity, making it of interest in pharmaceutical research. Its synthesis often involves the reaction of pyridazine derivatives with methanol and appropriate reagents to introduce the methoxy and carboxylate functionalities. As with many organic compounds, safety precautions should be observed when handling this substance due to potential toxicity and reactivity.

methyl 6-methoxypyridazine-3-carboxylate

19194-96-8: Methyl 6-methoxypyridazine-3-carboxylate, identified by its CAS number 19194-96-8, is an organic compound characterized by its pyridazine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms. This compound features a methoxy group (-OCH3) at the 6-position and a carboxylate ester group (-COOCH3) at the 3-position, contributing to its chemical reactivity and potential applications. It is typically a colorless to pale yellow liquid or solid, depending on its purity and form. The presence of the methoxy group enhances its solubility in organic solvents, while the carboxylate moiety can participate in various chemical reactions, such as esterification and nucleophilic substitutions. Methyl 6-methoxypyridazine-3-carboxylate may exhibit biological activity, making it of interest in pharmaceutical research. Its synthesis often involves the reaction of pyridazine derivatives with methanol and appropriate reagents to introduce the methoxy and carboxylate functionalities. As with many organic compounds, safety precautions should be observed when handling this substance due to potential toxicity and reactivity.

CAS 19194-96-8

methyl 6-methoxypyridazine-3-carboxylate

6-Methoxypyridazine-3-carboxylic acid methyl ester

Ref: IN-DA01WZKI

6-Methoxypyridazine-3-carboxylic acid methyl ester

Ref: 54-OR76432

METHYL 6-METHOXYPYRIDAZINE-3-CARBOXYLATE

Ref: 10-F537035