4-Chlorothieno[2,3-b]pyridin-6(7H)-one is a heterocyclic organic compound characterized by its fused thieno and pyridine rings, which contribute to its unique chemical properties. The presence of a chlorine atom at the 4-position of the thieno ring enhances its reactivity and solubility in various organic solvents. This compound typically exhibits a pale yellow to brownish color and has a relatively low molecular weight. It is known for its potential biological activities, making it of interest in medicinal chemistry and drug development. The compound's structure allows for various functionalizations, which can lead to derivatives with enhanced pharmacological properties. Additionally, it may participate in various chemical reactions, including nucleophilic substitutions and cycloadditions, due to the electron-withdrawing nature of the chlorine substituent. Its stability and reactivity can be influenced by environmental factors such as pH and temperature, making it important to consider these conditions in practical applications. Overall, 4-Chlorothieno[2,3-b]pyridin-6(7H)-one is a versatile compound with significant implications in chemical research and development.

4-Chlorothieno[2,3-b]pyridin-6(7H)-one

99429-81-9: 4-Chlorothieno[2,3-b]pyridin-6(7H)-one, Thieno[2,3-b]pyridin-6(7H)-one, 4-chloro-

CAS 99429-81-9: 4-Chlorothieno[2,3-b]pyridin-6(7H)-one

4-Chloro-6H,7H-thieno[2,3-b]pyridin-6-one

Ref: 3D-ZDA42981

4-Chlorothieno[2,3-b]pyridin-6(7H)-one

Ref: IN-DA01ED9O