3-Pyridinecarboxylic acid, 5-fluoro-6-methoxy- 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 (-COOH) at the 3-position, a fluorine atom at the 5-position, and a methoxy group (-OCH3) at the 6-position of the pyridine ring. The presence of these substituents influences its chemical reactivity and physical properties, such as solubility and boiling point. Typically, compounds like this may exhibit biological activity, making them of interest in pharmaceutical research. The fluorine atom can enhance lipophilicity and metabolic stability, while the methoxy group may affect the compound's electronic properties. As with many pyridine derivatives, this compound may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in synthetic organic chemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

3-pyridinecarboxylic acid, 5-fluoro-6-methoxy-

953780-42-2: 3-Pyridinecarboxylic acid, 5-fluoro-6-methoxy- 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 (-COOH) at the 3-position, a fluorine atom at the 5-position, and a methoxy group (-OCH3) at the 6-position of the pyridine ring. The presence of these substituents influences its chemical reactivity and physical properties, such as solubility and boiling point. Typically, compounds like this may exhibit biological activity, making them of interest in pharmaceutical research. The fluorine atom can enhance lipophilicity and metabolic stability, while the methoxy group may affect the compound's electronic properties. As with many pyridine derivatives, this compound may participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in synthetic organic chemistry. Safety and handling precautions should be observed, as with all chemical substances, due to potential toxicity or reactivity.

CAS 953780-42-2

3-pyridinecarboxylic acid, 5-fluoro-6-methoxy-

5-Fluoro-6-methoxypyridine-3-carboxylic acid

Ref: IN-DA00IJ0G

5-Fluoro-6-methoxypyridine-3-carboxylic acid

Ref: 54-PC99756

5-Fluoro-6-methoxynicotinic acid

Ref: 10-F220500