2,4-Dibromopyridine-3-carboxaldehyde is an organic compound characterized by its pyridine ring substituted with two bromine atoms and an aldehyde functional group. The presence of bromine atoms at the 2 and 4 positions of the pyridine ring enhances its reactivity and can influence its biological activity, making it of interest in medicinal chemistry. The carboxaldehyde group at the 3-position contributes to its potential as a versatile building block in organic synthesis, allowing for further functionalization. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its molecular structure suggests potential applications in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. Additionally, the compound's reactivity can be attributed to the electrophilic nature of the aldehyde group, which can participate in various chemical reactions, including nucleophilic additions and condensation reactions. Safety precautions should be taken when handling this compound, as brominated compounds can be hazardous.

2,4-Dibromopyridine-3-carboxaldehyde

128071-91-0: 2,4-DiBromonicotincarboxaldehyde, 2,4-DiBromopyridin-3-ylcarboxaldehyde

CAS 128071-91-0: 2,4-Dibromopyridine-3-carboxaldehyde

2,4-Dibromonicotinaldehyde

Ref: 10-F461986

2,4-Dibromopyridine-3-carboxaldehyde

Ref: 3D-DFA07191

3-Pyridinecarboxaldehyde, 2,4-dibromo-

Ref: IN-DA000XQ7

2,4-Dibromopyridine-3-carboxaldehyde

Ref: FT-Y15209

2,4-Dibromonicotinaldehyde

Ref: 54-OR18836