Pyridazine-4-carbaldehyde, with the CAS number 50901-42-3, is an organic compound characterized by its pyridazine ring structure, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 2. The aldehyde functional group (-CHO) is located at the 4-position of the pyridazine ring, contributing to its reactivity and potential applications in organic synthesis. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its purity and conditions. Pyridazine-4-carbaldehyde is known for its role as an intermediate in the synthesis of various pharmaceuticals and agrochemicals, owing to its ability to participate in nucleophilic addition reactions. It may exhibit moderate solubility in polar solvents like water and ethanol, while being less soluble in non-polar solvents. Safety data indicates that, like many aldehydes, it should be handled with care due to potential irritant properties. Overall, pyridazine-4-carbaldehyde is a valuable compound in the field of organic chemistry and medicinal chemistry.

pyridazine-4-carbaldehyde

Pyridazine-4-carboxaldehyde

Pyridazine-4-carboxaldehyde is a pyridine derivative that has been shown to have antiherpetic properties. It can be synthesized by reacting pyridazine with methyl iodide and anhydrous potassium carbonate. Pyridazine-4-carboxaldehyde is a potent inhibitor of human cytomegalovirus (HCMV) replication in cell culture, and its activity against the virus may be due to its ability to inhibit DNA synthesis and act as a cytotoxic agent. Pyridazine-4-carboxaldehyde has also been studied for its potential use in cancer treatment, with one study showing that it was able to inhibit tumor growth in mice.

CAS 50901-42-3: pyridazine-4-carbaldehyde

Pyridazine-4-carboxaldehyde

Ref: 54-OR59872

Pyridazine-4-carboxaldehyde

Ref: 3D-ACA90142

Pyridazine-4-carbaldehyde

Ref: 10-F236690

Pyridazine-4-carbaldehyde

Ref: IN-DA0037DP