Diethyl 1,2,3,6-tetrahydropyridazine-1,2-dicarboxylate is an organic compound characterized by its tetrahydropyridazine ring structure, which is a saturated six-membered ring containing two nitrogen atoms. This compound features two ester functional groups, as indicated by the diethyl dicarboxylate moiety, which contributes to its reactivity and solubility properties. Typically, such compounds exhibit moderate polarity due to the presence of the ester groups, making them soluble in organic solvents like ethanol and acetone, while being less soluble in water. The presence of the tetrahydropyridazine ring may impart specific biological activities, making it of interest in medicinal chemistry. Additionally, the compound may participate in various chemical reactions, including esterification and nucleophilic substitutions, due to the reactive nature of the carboxylate groups. Safety data sheets should be consulted for handling and storage guidelines, as with any chemical substance, to ensure proper safety measures are taken. Overall, diethyl 1,2,3,6-tetrahydropyridazine-1,2-dicarboxylate is a versatile compound with potential applications in organic synthesis and pharmaceuticals.

diethyl 1,2,3,6-tetrahydropyridazine-1,2-dicarboxylate

35691-30-6: Diethyl 1,2,3,6-tetrahydropyridazine-1,2-dicarboxylate is an organic compound characterized by its tetrahydropyridazine ring structure, which is a saturated six-membered ring containing two nitrogen atoms. This compound features two ester functional groups, as indicated by the diethyl dicarboxylate moiety, which contributes to its reactivity and solubility properties. Typically, such compounds exhibit moderate polarity due to the presence of the ester groups, making them soluble in organic solvents like ethanol and acetone, while being less soluble in water. The presence of the tetrahydropyridazine ring may impart specific biological activities, making it of interest in medicinal chemistry. Additionally, the compound may participate in various chemical reactions, including esterification and nucleophilic substitutions, due to the reactive nature of the carboxylate groups. Safety data sheets should be consulted for handling and storage guidelines, as with any chemical substance, to ensure proper safety measures are taken. Overall, diethyl 1,2,3,6-tetrahydropyridazine-1,2-dicarboxylate is a versatile compound with potential applications in organic synthesis and pharmaceuticals.

CAS 35691-30-6

diethyl 1,2,3,6-tetrahydropyridazine-1,2-dicarboxylate

diethyl 1,2,3,6-tetrahydropyridazine-1,2-dicarboxylate

Ref: 54-OR25569