3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine is a heterocyclic compound characterized by its unique bicyclic structure that incorporates both triazole and pyridazine moieties. This compound features two chlorine atoms at the 3 and 6 positions of the triazole ring, which can significantly influence its chemical reactivity and biological activity. The presence of these halogen substituents often enhances lipophilicity and can affect the compound's interaction with biological targets. 3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine is typically synthesized through multi-step organic reactions, and its properties may include moderate solubility in organic solvents and potential applications in pharmaceuticals or agrochemicals due to its structural characteristics. The compound's reactivity can be attributed to the electron-withdrawing nature of the chlorine atoms, which may facilitate nucleophilic attack in various chemical reactions. As with many heterocycles, it may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry research.

3,6-dichloro[1,2,4]triazolo[4,3-b]pyridazine

33050-38-3: 3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine is a heterocyclic compound characterized by its unique bicyclic structure that incorporates both triazole and pyridazine moieties. This compound features two chlorine atoms at the 3 and 6 positions of the triazole ring, which can significantly influence its chemical reactivity and biological activity. The presence of these halogen substituents often enhances lipophilicity and can affect the compound's interaction with biological targets. 3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine is typically synthesized through multi-step organic reactions, and its properties may include moderate solubility in organic solvents and potential applications in pharmaceuticals or agrochemicals due to its structural characteristics. The compound's reactivity can be attributed to the electron-withdrawing nature of the chlorine atoms, which may facilitate nucleophilic attack in various chemical reactions. As with many heterocycles, it may exhibit interesting pharmacological properties, making it a subject of interest in medicinal chemistry research.

3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine

<p>3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine</p>

CAS 33050-38-3

3,6-dichloro[1,2,4]triazolo[4,3-b]pyridazine

3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine

Ref: IN-DA00BZIB

3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine

Ref: 54-OR15258

3,6-Dichloro[1,2,4]triazolo[4,3-b]pyridazine

Ref: 10-F067629