1-(Oxazol-2-yl)ethanone, with the CAS number 77311-07-0, is an organic compound characterized by the presence of an oxazole ring, which is a five-membered heterocyclic structure containing both nitrogen and oxygen atoms. This compound typically exhibits a polar nature due to the electronegative atoms in its structure, influencing its solubility in various solvents. It is often used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. The oxazole moiety can impart unique reactivity, making it a valuable building block in the development of biologically active compounds. Additionally, the presence of the ethanone functional group suggests potential reactivity in nucleophilic addition reactions. Overall, 1-(Oxazol-2-yl)ethanone is notable for its heterocyclic structure, which contributes to its chemical properties and potential applications in synthetic chemistry.

1-(Oxazol-2-yl)ethanone

77311-07-0: 1-(1,3-Oxazol-2-yl)ethan-1-one, 1-(1,3-Oxazol-2-yl)ethanone, 1-(2-Oxazolyl)ethanone, 1-(Oxazole-2-yl)ethanone, 2-Acetyloxazole, Ethanone, 1-(2-oxazolyl)-, Ethanone, 1-(2-oxazolyl)- (9CI), 1-(Oxazol-2-yl)ethanone, 1-(OXAZOL-2-YL)ETHANONE

1-(Oxazol-2-yl)ethanone is a benzyl compound that can be thermally induced to react with an aminophenol and a quinone to form coumarin. It belongs to the group of phenolic compounds. 1-(Oxazol-2-yl)ethanone has been found in the leaves of many plants and also in certain fungi, such as Aspergillus niger.

Applications 1-(Oxazol-2-yl)ethanone is a benzimidazole derivatives which is used as regulators of steroid receptor coactivators
References O'Malley, Bert W. et al.,PCT Int. Appl. (2017);


CAS 77311-07-0: 1-(Oxazol-2-yl)ethanone

1-(Oxazol-2-yl)ethanone

Ref: IN-DA005CZA

1-(Oxazol-2-yl)ethanone

Ref: 3D-FO140886

1-(Oxazol-2-yl)ethanone

Ref: TR-O991018

1-(Oxazol-2-yl)ethanone

Ref: 10-F091904