3-Bromo-5-quinolinecarboxylic acid is an organic compound characterized by its quinoline structure, which consists of a bicyclic aromatic system containing a nitrogen atom. The presence of a bromine atom at the 3-position and a carboxylic acid functional group at the 5-position contributes to its unique chemical properties. This compound is typically a solid at room temperature and is soluble in polar organic solvents. It exhibits acidic behavior due to the carboxylic acid group, allowing it to participate in various chemical reactions, such as esterification and amidation. The bromine substituent can also serve as a site for further functionalization, making it a versatile intermediate in organic synthesis. Additionally, compounds of this nature may exhibit biological activity, potentially serving as precursors for pharmaceuticals or agrochemicals. Safety data should be consulted for handling and storage, as halogenated compounds can pose environmental and health risks. Overall, 3-Bromo-5-quinolinecarboxylic acid is a significant compound in both synthetic organic chemistry and medicinal chemistry research.

3-Bromo-5-quinolinecarboxylic acid

1344046-12-3: 3-Bromo-5-quinolinecarboxylic acid, 5-Quinolinecarboxylic acid, 3-bromo-, 3-Bromoquinoline-5-carboxylic acid

CAS 1344046-12-3: 3-Bromo-5-quinolinecarboxylic acid

3-Bromoquinoline-5-carboxylic acid

Ref: 10-F464642

3-Bromoquinoline-5-carboxylic acid

Ref: 54-OR300389

3-bromoquinoline-5-carboxylic acid

Ref: IN-DA009DF4

3-Bromoquinoline-5-carboxylic acid

Ref: FT-B13574