4-Benzoylbiphenyl

CAS: 2128-93-0

Ref. 3D-FB34281

Produktinformation

• Name: 4-Benzoylbiphenyl
• Synonyme: ((1,1-Biphenyl)-4-yl)phenylmethanone, 4-(Phenylcarbonyl)biphenyl, 4-Benzoyl-1,1′-biphenyl, 4-Benzoylbiphenyl[1,1'-biphenyl]-4-ylphenyl-Methanone, 4-Biphenylyl phenyl ketone, 4-Phenybenzophenone, 4-Phenyl Benzophenone, 4-Phenyl benzopehone, 4-Phenylbenzophenone, 4-Phenylphenyl phenyl methanone, Benzophenone, 4-phenyl-, Biphenyl-4-Yl(Phenyl)Methanone, Eusolex 3490, Gencure PBZ, Genocure PBZ, JRcure PBZ, Methanone, [1,1′-biphenyl]-4-ylphenyl-, NSC 55283, NSC 97365, Phenyl p-biphenylyl ketone, Photoinitiator-PBZ, Runtecure 1059, Speedcure BPZ, Speedcure PBZ, Trigonal 12, [1,1'-biphenyl]-4-ylphenyl-Methanone, [1,1′-Biphenyl]-4-ylphenylmethanone, p-Benzoylbiphenyl, p-Biphenylyl phenyl ketone, p-Phenyl Benzophenone, p-Phenylbenzophenone
• CAS: 2128-93-0

Beschreibung

4-Benzoylbiphenyl is an analytical method that is used to study the structure of organic compounds. This technique exploits the reactivity of chlorine atoms and biphenyl to produce a unique reaction intermediate. The fluorescence characteristic of this intermediate can be measured by FT-IR spectroscopy and is used to determine the structural properties of organic compounds. 4-Benzoylbiphenyl has been shown to have intramolecular hydrogen bonding, which may result in a matrix effect when it is used as a stationary phase in thin layer chromatography. This compound also has photochemical properties, which means it will undergo photoelimination reactions when exposed to light or UV radiation. 4-Benzoylbiphenyl is soluble in organic solvents and has an electron donating property due to its carbonyl group.

• Marke: Biosynth

Chemische Eigenschaften

• Molekulargewicht: 258.31 g/mol
• Formel: C₁₉H₁₄O
• Reinheit: Min. 95%