3-Pyridinecarboxylic acid, 6-amino-2-methyl-, methyl ester, also known by its CAS number 872355-52-7, is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a carboxylic acid functional group that has been esterified with methanol, resulting in a methyl ester. The presence of an amino group at the 6-position and a methyl group at the 2-position of the pyridine ring contributes to its unique chemical properties. Typically, such compounds exhibit moderate polarity due to the functional groups, which can influence their solubility in various solvents. They may also participate in hydrogen bonding, affecting their reactivity and interactions with biological systems. The compound's structure suggests potential applications in pharmaceuticals or agrochemicals, where modifications to the pyridine ring can enhance biological activity or selectivity. As with many organic compounds, safety data should be consulted for handling and usage, as they may pose health or environmental risks.

3-pyridinecarboxylic acid, 6-amino-2-methyl-, methyl ester

872355-52-7: 3-Pyridinecarboxylic acid, 6-amino-2-methyl-, methyl ester, also known by its CAS number 872355-52-7, is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features a carboxylic acid functional group that has been esterified with methanol, resulting in a methyl ester. The presence of an amino group at the 6-position and a methyl group at the 2-position of the pyridine ring contributes to its unique chemical properties. Typically, such compounds exhibit moderate polarity due to the functional groups, which can influence their solubility in various solvents. They may also participate in hydrogen bonding, affecting their reactivity and interactions with biological systems. The compound's structure suggests potential applications in pharmaceuticals or agrochemicals, where modifications to the pyridine ring can enhance biological activity or selectivity. As with many organic compounds, safety data should be consulted for handling and usage, as they may pose health or environmental risks.

CAS 872355-52-7

3-pyridinecarboxylic acid, 6-amino-2-methyl-, methyl ester

Methyl 6-amino-2-methylnicotinate

Ref: IN-DA00GTGH

Methyl 6-amino-2-methylnicotinate

Ref: 54-OR510089

Methyl 6-amino-2-methylnicotinate

Ref: 10-F603307