2,6-Dibromopyridine-4-carbaldehyde is an organic compound characterized by its pyridine ring, which is substituted at the 2 and 6 positions with bromine atoms and at the 4 position with a formyl group (–CHO). This compound typically appears as a solid or liquid, depending on the specific conditions, and is known for its distinctive aromatic properties due to the presence of the pyridine ring. The bromine substituents enhance its reactivity, making it useful in various chemical synthesis applications, particularly in the development of pharmaceuticals and agrochemicals. The aldehyde functional group contributes to its reactivity, allowing it to participate in condensation reactions and serve as a precursor for further chemical modifications. Additionally, 2,6-dibromopyridine-4-carbaldehyde may exhibit biological activity, which can be explored in medicinal chemistry. Its solubility in organic solvents and stability under standard laboratory conditions make it a valuable compound in synthetic organic chemistry. Safety precautions should be observed when handling this compound due to the presence of bromine, which can be hazardous.

2,6-dibromopyridine-4-carbaldehyde

316800-46-1: 2,6-Dibromopyridine-4-carbaldehyde is an organic compound characterized by its pyridine ring, which is substituted at the 2 and 6 positions with bromine atoms and at the 4 position with a formyl group (–CHO). This compound typically appears as a solid or liquid, depending on the specific conditions, and is known for its distinctive aromatic properties due to the presence of the pyridine ring. The bromine substituents enhance its reactivity, making it useful in various chemical synthesis applications, particularly in the development of pharmaceuticals and agrochemicals. The aldehyde functional group contributes to its reactivity, allowing it to participate in condensation reactions and serve as a precursor for further chemical modifications. Additionally, 2,6-dibromopyridine-4-carbaldehyde may exhibit biological activity, which can be explored in medicinal chemistry. Its solubility in organic solvents and stability under standard laboratory conditions make it a valuable compound in synthetic organic chemistry. Safety precautions should be observed when handling this compound due to the presence of bromine, which can be hazardous.

CAS 316800-46-1

2,6-dibromopyridine-4-carbaldehyde

2,6-Bibromopyridine-4-carbaldehyde

Ref: IN-DA007IRI

2,6-Dibromoisonicotinaldehyde

Ref: 54-OR18033

2,6-Dibromopyridine-4-carboxaldehyde

Ref: 10-F631869