2-Bromo-4-phenylphenol, with the CAS number 92-03-5, is an organic compound characterized by its aromatic structure, which includes a bromine atom and a hydroxyl group attached to a biphenyl framework. This compound typically appears as a white to light yellow solid and is known for its moderate solubility in organic solvents, while being less soluble in water. It exhibits properties typical of phenolic compounds, such as the ability to act as an antioxidant and antimicrobial agent. The presence of the bromine atom enhances its reactivity, making it useful in various chemical syntheses and applications, including as an intermediate in the production of dyes and pharmaceuticals. Additionally, 2-Bromo-4-phenylphenol can undergo electrophilic substitution reactions due to its electron-rich aromatic system. Safety considerations should be taken into account when handling this compound, as it may pose health risks if ingested or inhaled, and appropriate protective measures should be employed in laboratory settings.

2-Bromo-4-phenylphenol

92-03-5: , [1,1′-Biphenyl]-4-ol, 3-bromo-, 4-Biphenylol, 3-bromo-, Phenol, 2-bromo-4-phenyl-, 2-Bromo-4-phenylphenol, 3-Bromo[1,1′-biphenyl]-4-ol

3-Bromo-[1,1Õ-Biphenyl]-4-Ol

3-Bromo[1,1'-biphenyl]-4-ol is a betaine metabolite that is formed by the oxidation of choline or trimethylamine. It can be detected by microscopy in a variety of biological samples. 3-Bromo[1,1'-biphenyl]-4-ol has been used as an immunosensor for environmental monitoring and identification of typhimurium in food. This metabolite can be used as an amplifier to increase the sensitivity of electrochemical detection and is also amenable to linear range detection. 3-Bromo[1,1'-biphenyl]-4-ol has been shown to be catalysed by arenes such as naphthalene or anthracene.

CAS 92-03-5: 2-Bromo-4-phenylphenol

3-Bromo-[1,1Õ-Biphenyl]-4-Ol

Ref: 54-OR1029494

3-Bromo[1,1'-biphenyl]-4-ol

Ref: 3D-AAA09203

3-BROMO-4-HYDROXYDIPHENYL

Ref: IN-DA00GYFG

3-Bromo-biphenyl-4-ol

Ref: 10-F603811