Diethyl 5-bromopyridine-2,3-dicarboxylate is an organic compound characterized by its pyridine ring substituted with bromine and two ester functional groups. The presence of the bromine atom at the 5-position of the pyridine ring enhances its reactivity, making it useful in various synthetic applications, particularly in the field of medicinal chemistry and organic synthesis. The two carboxylate groups, derived from diethyl esterification, contribute to the compound's polar nature, influencing its solubility in polar solvents. This compound typically exhibits moderate stability under standard conditions but may undergo hydrolysis in the presence of strong bases or acids. Its molecular structure allows for potential interactions with biological targets, making it a candidate for further research in drug development. Additionally, the compound's unique properties can facilitate its use in coupling reactions or as a building block in the synthesis of more complex molecules. Safety precautions should be observed when handling this compound due to its bromine content, which can pose health risks.

diethyl 5-bromopyridine-2,3-dicarboxylate

110239-01-5: Diethyl 5-bromopyridine-2,3-dicarboxylate is an organic compound characterized by its pyridine ring substituted with bromine and two ester functional groups. The presence of the bromine atom at the 5-position of the pyridine ring enhances its reactivity, making it useful in various synthetic applications, particularly in the field of medicinal chemistry and organic synthesis. The two carboxylate groups, derived from diethyl esterification, contribute to the compound's polar nature, influencing its solubility in polar solvents. This compound typically exhibits moderate stability under standard conditions but may undergo hydrolysis in the presence of strong bases or acids. Its molecular structure allows for potential interactions with biological targets, making it a candidate for further research in drug development. Additionally, the compound's unique properties can facilitate its use in coupling reactions or as a building block in the synthesis of more complex molecules. Safety precautions should be observed when handling this compound due to its bromine content, which can pose health risks.

Diethyl 5-bromopyridine-2,3-dicarboxylate

CAS 110239-01-5

diethyl 5-bromopyridine-2,3-dicarboxylate

Diethyl 5-bromopyridine-2,3-dicarboxylate

Ref: 54-OR1057906