Propane-1,3-diyl dipyridine-3-carboxylate, identified by its CAS number 98326-19-3, is an organic compound characterized by its structure, which includes a propane backbone with two pyridine-3-carboxylate groups attached. This compound typically exhibits properties associated with esters, such as being a colorless to pale yellow liquid or solid, depending on its specific form and purity. It is likely to be soluble in organic solvents, reflecting the polar nature of the pyridine rings and the ester functional groups. The presence of the pyridine moieties suggests potential applications in coordination chemistry, as they can act as ligands for metal ions. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its stability and reactivity can be influenced by the functional groups present, and it may participate in various chemical reactions typical of esters, such as hydrolysis or transesterification. Overall, propane-1,3-diyl dipyridine-3-carboxylate is a versatile compound with potential applications in both industrial and research settings.

propane-1,3-diyl dipyridine-3-carboxylate

98326-19-3: Propane-1,3-diyl dipyridine-3-carboxylate, identified by its CAS number 98326-19-3, is an organic compound characterized by its structure, which includes a propane backbone with two pyridine-3-carboxylate groups attached. This compound typically exhibits properties associated with esters, such as being a colorless to pale yellow liquid or solid, depending on its specific form and purity. It is likely to be soluble in organic solvents, reflecting the polar nature of the pyridine rings and the ester functional groups. The presence of the pyridine moieties suggests potential applications in coordination chemistry, as they can act as ligands for metal ions. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Its stability and reactivity can be influenced by the functional groups present, and it may participate in various chemical reactions typical of esters, such as hydrolysis or transesterification. Overall, propane-1,3-diyl dipyridine-3-carboxylate is a versatile compound with potential applications in both industrial and research settings.

<p>3,3′-(1,3-Propanediyl) di-3-pyridinecarboxylate</p>

CAS 98326-19-3

propane-1,3-diyl dipyridine-3-carboxylate

3,3′-(1,3-Propanediyl) di-3-pyridinecarboxylate

Ref: 54-OR1035977

3,3′-(1,3-Propanediyl) di-3-pyridinecarboxylate

Ref: 10-F556173