6-Chloro-3-methylimidazo[2,1-b][1,3]thiazole-5-carbaldehyde is a heterocyclic organic compound characterized by its complex structure, which includes an imidazole ring fused to a thiazole ring. The presence of a chloro substituent and a carbaldehyde functional group contributes to its reactivity and potential applications in various chemical reactions. This compound is typically used in research settings, particularly in studies related to medicinal chemistry and the synthesis of biologically active molecules. Its unique structure may impart specific biological activities, making it of interest in pharmacological investigations. The compound is likely to exhibit properties such as moderate solubility in organic solvents and stability under standard laboratory conditions. However, due to the presence of reactive functional groups, it may require careful handling and storage to prevent degradation or unwanted reactions. As with many heterocycles, it may also participate in various chemical transformations, making it a valuable intermediate in synthetic organic chemistry.

6-chloro-3-methylimidazo[2,1-b][1,3]thiazole-5-carbaldehyde

178449-63-3: 6-Chloro-3-methylimidazo[2,1-b][1,3]thiazole-5-carbaldehyde is a heterocyclic organic compound characterized by its complex structure, which includes an imidazole ring fused to a thiazole ring. The presence of a chloro substituent and a carbaldehyde functional group contributes to its reactivity and potential applications in various chemical reactions. This compound is typically used in research settings, particularly in studies related to medicinal chemistry and the synthesis of biologically active molecules. Its unique structure may impart specific biological activities, making it of interest in pharmacological investigations. The compound is likely to exhibit properties such as moderate solubility in organic solvents and stability under standard laboratory conditions. However, due to the presence of reactive functional groups, it may require careful handling and storage to prevent degradation or unwanted reactions. As with many heterocycles, it may also participate in various chemical transformations, making it a valuable intermediate in synthetic organic chemistry.

CAS 178449-63-3

6-chloro-3-methylimidazo[2,1-b][1,3]thiazole-5-carbaldehyde

Imidazo[2,1-b]thiazole-5-carboxaldehyde, 6-chloro-3-methyl-

Ref: IN-DA002629

6-chloro-3-methylimidazo[2,1-b][1,3]thiazole-5-carbaldehyde

Ref: 10-F311409