1-(7-acetyl-9H-fluoren-2-yl)ethan-1-one, with the CAS number 961-27-3, is an organic compound characterized by its structure, which features a fluorenyl moiety substituted with an acetyl group and an ethyl ketone functional group. This compound typically appears as a solid at room temperature and is known for its aromatic properties due to the presence of the fluorenyl ring, which contributes to its stability and potential reactivity. The acetyl group introduces a carbonyl functionality, making it a ketone, which can participate in various chemical reactions, such as nucleophilic additions. Its unique structure may impart specific optical properties, making it of interest in fields such as materials science and organic synthesis. Additionally, the compound may exhibit biological activity, although specific studies would be required to elucidate its pharmacological properties. As with many organic compounds, proper handling and safety precautions should be observed due to potential toxicity or reactivity.

1-(7-acetyl-9H-fluoren-2-yl)ethan-1-one

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Applications 2,7-Diacetylfluorene is used as a reactant in the synthesis of (dioxaborine)fluorene derivatives for light-emitting diodes (LEDs).
References Domercq, B., et al.: J. Phys. Chem. B, 108, 8647 (2004);


2,7-Diacetylfluorene

2,7-Diacetylfluorene is an antibiotic that inhibits bacterial growth by binding to the succinoyl group of the enzyme DNA gyrase. 2,7-Diacetylfluorene has been shown to be toxic in a number of different experimental systems, including luminescent bacteria and cells from calf thymus. It is also shown to be carcinogenic in rats.

CAS 961-27-3: 1-(7-acetyl-9H-fluoren-2-yl)ethan-1-one

2,7-Diacetylfluorene

Ref: TR-D353240

2,7-Diacetylfluorene

Ref: 3D-FD158955

2,7-Diacetylfluorene

Ref: 54-OR0328

2,7-Diacetylfluorene

Ref: 10-F002539

2,7-DIACETYLFLUORENE

Ref: IN-DA003G6K

2,7-Diacetylfluorene

Ref: 3B-D2863