3-Bromofluoren-9-one is an organic compound characterized by its structure, which features a bromine atom and a ketone functional group attached to a fluorenone framework. This compound typically appears as a solid at room temperature and is known for its aromatic properties due to the presence of the fluorenone moiety. The bromine substituent introduces both steric and electronic effects, influencing its reactivity and interactions in various chemical reactions. 3-Bromofluoren-9-one is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, due to its ability to participate in electrophilic aromatic substitution reactions. Additionally, it can serve as a precursor for the synthesis of other complex organic molecules. Its physical properties, such as solubility and melting point, can vary depending on the solvent and conditions used. As with many brominated compounds, it is important to handle 3-bromofluoren-9-one with care, considering potential toxicity and environmental impact.

3-bromofluoren-9-one

2041-19-2: 3-Bromo-9H-fluoren-9-one, 3-Bromo-9-Fluorenone

3-Bromo-9H-fluoren-9-one is a fluorescent dye that is used to measure the transport properties of cells. It can be activated by light and fluoresces at a wavelength of 527 nm, with an emission maximum at 575 nm. 3-Bromo-9H-fluoren-9-one has two isomers: cis and trans. The trans isomer has a higher photophysical nature, as it absorbed less light than the cis form. The molecule also has linkages to other molecules such as proteins, nucleic acids, carbohydrates, lipids, or synthetic polymers. 3Bromo-9H-fluoren-9-one can be modulated by changing its parameters such as temperature and concentration.

CAS 2041-19-2: 3-bromofluoren-9-one

3-Bromo-9H-fluoren-9-one

Ref: 3D-CAA04119

3-Bromo-9H-fluoren-9-one

Ref: 10-F540470

3-Bromo-9H-fluoren-9-one

Ref: IN-DA00BGKP

3-Bromo-9H-fluoren-9-one

Ref: 54-OR50971

3-Bromo-9H-fluoren-9-one

Ref: 3B-B5673