6-Chloro-imidazo[1,2-b]pyridazine-3-carbonitrile is a heterocyclic compound characterized by its unique bicyclic structure, which incorporates both imidazole and pyridazine rings. The presence of a chlorine atom at the 6-position and a carbonitrile group at the 3-position contributes to its chemical reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the imidazole and pyridazine moieties, which are often associated with various biological activities. The carbonitrile functional group can also enhance the compound's ability to participate in nucleophilic reactions. Additionally, the compound's properties, such as melting point, boiling point, and spectral characteristics, can be influenced by the presence of the chlorine substituent and the overall electronic configuration of the molecule. Overall, 6-chloro-imidazo[1,2-b]pyridazine-3-carbonitrile is of interest for further research in both synthetic and medicinal chemistry.

6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-3-CARBONITRILE

123531-54-4: 6-Chloro-imidazo[1,2-b]pyridazine-3-carbonitrile is a heterocyclic compound characterized by its unique bicyclic structure, which incorporates both imidazole and pyridazine rings. The presence of a chlorine atom at the 6-position and a carbonitrile group at the 3-position contributes to its chemical reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar organic solvents. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to the presence of the imidazole and pyridazine moieties, which are often associated with various biological activities. The carbonitrile functional group can also enhance the compound's ability to participate in nucleophilic reactions. Additionally, the compound's properties, such as melting point, boiling point, and spectral characteristics, can be influenced by the presence of the chlorine substituent and the overall electronic configuration of the molecule. Overall, 6-chloro-imidazo[1,2-b]pyridazine-3-carbonitrile is of interest for further research in both synthetic and medicinal chemistry.

Imidazo[1,2-b]pyridazine-3-carbonitrile, 6-chloro-

<p>6-Chloroimidazo[1,2-b]pyridazine-3-carbonitrile</p>

CAS 123531-54-4

6-CHLORO-IMIDAZO[1,2-B]PYRIDAZINE-3-CARBONITRILE

Imidazo[1,2-b]pyridazine-3-carbonitrile, 6-chloro-

Ref: IN-DA000KR3

6-Chloroimidazo[1,2-b]pyridazine-3-carbonitrile

Ref: 54-OR940590

6-Chloroimidazo[1,2-b]pyridazine-3-carbonitrile

Ref: 10-F604404