Methyl 5-methylpyridazine-4-carboxylate is an organic compound characterized by its pyridazine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms. This compound features a carboxylate functional group, indicating it is an ester, specifically a methyl ester, due to the presence of a methyl group attached to the carboxylic acid moiety. The presence of the 5-methyl substituent on the pyridazine ring contributes to its unique chemical properties, potentially influencing its reactivity and solubility. Methyl 5-methylpyridazine-4-carboxylate may exhibit moderate polarity due to the carboxylate group, making it soluble in polar solvents while retaining some hydrophobic characteristics from the methyl groups. This compound may be of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential biological activity and utility as a synthetic intermediate. Its specific reactivity and applications would depend on further studies and characterization, including its behavior in different chemical environments.

methyl 5-methylpyridazine-4-carboxylate

1363383-02-1: Methyl 5-methylpyridazine-4-carboxylate is an organic compound characterized by its pyridazine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms. This compound features a carboxylate functional group, indicating it is an ester, specifically a methyl ester, due to the presence of a methyl group attached to the carboxylic acid moiety. The presence of the 5-methyl substituent on the pyridazine ring contributes to its unique chemical properties, potentially influencing its reactivity and solubility. Methyl 5-methylpyridazine-4-carboxylate may exhibit moderate polarity due to the carboxylate group, making it soluble in polar solvents while retaining some hydrophobic characteristics from the methyl groups. This compound may be of interest in various fields, including pharmaceuticals and agrochemicals, due to its potential biological activity and utility as a synthetic intermediate. Its specific reactivity and applications would depend on further studies and characterization, including its behavior in different chemical environments.

4-Pyridazinecarboxylic acid, 5-methyl-, methyl ester

<p>Methyl 5-methylpyridazine-4-carboxylate</p>

CAS 1363383-02-1

methyl 5-methylpyridazine-4-carboxylate

4-Pyridazinecarboxylic acid, 5-methyl-, methyl ester

Ref: IN-DA0011QO

Methyl 5-methylpyridazine-4-carboxylate

Ref: 54-OR1022245

METHYL 5-METHYLPYRIDAZINE-4-CARBOXYLATE

Ref: 10-F467992