4,7-Dichloroquinoline-3-carboxylic acid is an organic compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. This compound features two chlorine substituents at the 4 and 7 positions of the quinoline ring, and a carboxylic acid functional group at the 3 position. The presence of these functional groups contributes to its chemical reactivity and potential applications in various fields, including pharmaceuticals and agrochemicals. The dichloro substitution enhances its biological activity, making it a subject of interest in medicinal chemistry. The compound is typically solid at room temperature and may exhibit moderate solubility in polar solvents due to the carboxylic acid group. Its molecular structure allows for potential interactions with biological targets, which can be explored for therapeutic purposes. As with many halogenated compounds, it is essential to consider its environmental impact and toxicity when evaluating its use in industrial applications.

4,7-dichloroquinoline-3-carboxylic acid

630067-21-9: 4,7-Dichloro-Quinoline-3-Carboxylic Acid

Hydroxychloroquine Impurity 15

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CAS 630067-21-9: 4,7-dichloroquinoline-3-carboxylic acid

Hydroxychloroquine Impurity 15

Ref: 4Z-H-0634

4,7-Dichloroquinoline-3-carboxylic acid

Ref: 3D-FAB06721

4,7-dichloroquinoline-3-carboxylic acid

Ref: IN-DA00EJB8

Hydroxychloroquine Impurity 11

Ref: ST-EA-CP-H4038