7190-81-0

Usage

Chemical compound

6-chloro-3-(4'-chlorophenyl)-[1,2,4]triazolo[4,3-b]pyridazine

Molecular structure

Contains two chlorine atoms, a triazolo ring, and a pyridazine ring

Heterocyclic compound

Has a ring structure with atoms of different elements (triatomic N-N-C-N ring)

Potential pharmaceutical applications

Due to its structural features and potential biological activity

Potential properties

Antibacterial, antifungal, antiviral, anticancer agent

Potential uses

Drug development, development of new pharmaceuticals, and agrochemicals

Need for further research and testing

To fully understand its properties and potential applications

Upstream product

• 7190-94-5 3-chlorobenzylidene-(6-chloro-3-pyridazinyl)-hydrazine 

Relevant academic research and scientific papers

A convenient new synthesis of fused 1,2,4-triazoles: The oxidation of heterocyclic hydrazones using copper dichloride

A series of 1,2,4-triazoles have been prepared by oxidative intramolecular cyclization of heterocyclic hydrazones with copper dichloride. General applicability of this simple transformation was confirmed by the synthesis of moderate to high yields of 1,2,

Synthesis and bioevaluation of 6-chloropyridazin-3-yl hydrazones and 6-chloro-3-substituted-[1,2,4]triazolo[4,3-b]pyridazines as cytotoxic agents

An efficient synthesis of a series of 6-chloro-3-substituted-[1,2,4]triazolo[4,3-b]pyridazines is described via intramolecular oxidative cyclization of various 6-chloropyridazin-3-yl hydrazones with iodobenzene diacetate. The structures of the newly synth