structure of Benzyl 4-[5-chloro-1-(2-ethoxy-2-oxoethyl)-6-oxo-1,6-dihydropyridazin-4-yl]piperazine-1-carboxylate

Benzyl 4-[5-chloro-1-(2-ethoxy-2-oxoethyl)-6-oxo-1,6-dihydropyridazin-4-yl]piperazine-1-carboxylate

CAS No.: 1000018-18-7
M. Wt: 434.9
M. Fa: C20H23ClN4O5
InChI Key: -

Names and Identifiers of 1000018-18-7

CAS Number

1000018-18-7

IUPAC Name

(phenylmethyl) 4-[5-chloranyl-1-(2-ethoxy-2-oxidanylidene-ethyl)-6-oxidanylidene-pyridazin-4-yl]piperazine-1-carboxylate

Canonical SMILES

CCOC(=O)CN1C(=O)C(=C(C=N1)N2CCN(CC2)C(=O)OCC3=CC=CC=C3)Cl

Physical and chemical properties of 1000018-18-7

Melting Point

116-117°C

Molecular Formula

C20H23ClN4O5

Molecular Weight

434.9

Applications of 1000018-18-7

Benzyl 4-[5-chloro-1-(2-ethoxy-2-oxoethyl)-6-oxo-1,6-dihydro-4-pyridazinyl]tetrahydro-1(2H)-pyrazinecarboxylate has potential applications in:

  • Pharmaceutical development, particularly in designing anticancer agents.
  • Chemical research, as a precursor or intermediate in synthesizing other complex organic molecules.

Its unique structural features make it suitable for further modifications that could enhance its biological activity or alter its pharmacokinetic properties.

Interaction Studies of 1000018-18-7

Interaction studies have indicated that Benzyl 4-[5-chloro-1-(2-ethoxy-2-oxoethyl)-6-oxo-1,6-dihydro-4-pyridazinyl]tetrahydro-1(2H)-pyrazinecarboxylate interacts with various biological targets within cellular systems. These interactions are crucial for understanding its mechanism of action and potential side effects when used therapeutically. Further studies are needed to elucidate these interactions fully and establish a pharmacological profile.

Biological Activity of 1000018-18-7

Research into the biological activity of Benzyl 4-[5-chloro-1-(2-ethoxy-2-oxoethyl)-6-oxo-1,6-dihydro-4-pyridazinyl]tetrahydro-1(2H)-pyrazinecarboxylate suggests potential anticancer properties. Studies have identified it as a candidate for further investigation due to its ability to inhibit cancer cell proliferation in multicellular spheroid models. The compound's unique structure allows it to interact with biological targets effectively, making it a subject of interest in pharmacological studies.