6-Chloro[1,3]oxazolo[4,5-b]pyridin-2(3H)-one is a heterocyclic compound characterized by its unique bicyclic structure, which incorporates both an oxazole and a pyridine moiety. This compound features a chlorine substituent at the 6-position of the oxazole ring, contributing to its chemical reactivity and potential biological activity. The presence of the oxazole ring imparts properties typical of nitrogen-containing heterocycles, such as the ability to participate in various chemical reactions, including nucleophilic substitutions and electrophilic additions. The compound is likely to exhibit moderate to high solubility in polar solvents due to its heteroatoms, which can engage in hydrogen bonding. Its structural features suggest potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, as compounds with similar frameworks have been explored for their biological activities. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the chlorine atom and the overall molecular geometry. As with many heterocycles, it may also serve as a building block for more complex organic synthesis.

6-chloro[1,3]oxazolo[4,5-b]pyridin-2(3H)-one

35570-68-4: oxazolo[4,5-b]pyridin-2(3H)-one, 6-chloro-, 6-Chlorooxazolo[4,5-b]pyridin-2(3H)-one

CAS 35570-68-4: 6-chloro[1,3]oxazolo[4,5-b]pyridin-2(3H)-one

6-Chlorooxazolo[4,5-b]pyridin-2(3H)-one

Ref: 54-OR939132

6-Chlorooxazolo[4,5-b]pyridin-2(3H)-one

Ref: 10-F214843

6-Chlorooxazolo[4,5-b]pyridin-2(3H)-one

Ref: IN-DA00CL64