N-(5-bromoquinolin-8-yl)acetamide is a chemical compound characterized by its structure, which includes a quinoline moiety substituted with a bromine atom at the 5-position and an acetamide functional group. This compound typically exhibits properties associated with both aromatic and amide functionalities, such as moderate solubility in organic solvents and potential reactivity due to the presence of the bromine atom, which can participate in nucleophilic substitution reactions. The quinoline ring system contributes to its potential biological activity, making it of interest in medicinal chemistry, particularly for its possible applications in drug development. The presence of the acetamide group may enhance its solubility and bioavailability. Additionally, compounds like N-(5-bromoquinolin-8-yl)acetamide may exhibit fluorescence properties, which can be useful in various analytical applications. Overall, this compound's unique structural features and functional groups make it a subject of interest for further research in both synthetic and applied chemistry contexts.

N-(5-bromoquinolin-8-yl)acetamide

99851-80-6: acetamide, N-(5-bromo-8-quinolinyl)-

N-(5-Bromoquinolin-8-yl)acetamide is a regioselective, site selective, and efficient synthetic intermediate for 8-aminoquinoline. It is synthesized from N-(5-bromoquinolin-8-yl)acetamide with the use of n-fluorobenzenesulfonimide in a transfer reaction. The bromine atom on the amide group is transferred to the nitro group on the 8-aminoquinoline ring, leading to a new amide group. This synthesis provides an efficient and scalable route to 8-aminoquinoline.

CAS 99851-80-6: N-(5-bromoquinolin-8-yl)acetamide

N-(5-Bromoquinolin-8-yl)acetamide

Ref: 3D-FB120257

N-(5-bromo-8-quinolinyl)acetamide

Ref: 10-F314582

N-(5-BROMO-8-QUINOLINYL)ACETAMIDE

Ref: IN-DA003W70