2,6-Dichloro-4-(trifluoromethyl)pyridine-3-carboxylic acid is a heterocyclic organic compound characterized by its pyridine ring, which is substituted at the 2 and 6 positions with chlorine atoms and at the 4 position with a trifluoromethyl group. Additionally, it contains a carboxylic acid functional group at the 3 position. This compound is typically a solid at room temperature and is known for its potential applications in pharmaceuticals and agrochemicals due to its unique structural features. The presence of both halogen substituents and the carboxylic acid group contributes to its reactivity and solubility in various solvents. Its molecular structure allows for various interactions, making it a candidate for further chemical modifications. The trifluoromethyl group enhances lipophilicity, which can influence the compound's biological activity. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks. Overall, 2,6-dichloro-4-(trifluoromethyl)pyridine-3-carboxylic acid is a compound of interest in synthetic chemistry and material science.

2,6-dichloro-4-(trifluoromethyl)pyridine-3-carboxylic acid

503437-19-2: 2,6-Dichloro-4-(Trifluoromethyl)Nicotinic Acid, 3-Pyridinecarboxylic acid, 2,6-dichloro-4-(trifluoromethyl)-

CAS 503437-19-2: 2,6-dichloro-4-(trifluoromethyl)pyridine-3-carboxylic acid

2,6-Dichloro-4-(trifluoromethyl)nicotinic acid

Ref: 10-F046533

2,6-Dichloro-4-(trifluoromethyl)nicotinic acid

Ref: IN-DA006UOU

2,6-Dichloro-4-(trifluoromethyl)nicotinic acid

Ref: 54-PC6153