CAS 88372-92-3

bis(4-chlorophenyl)ethanedione

Description:

Bis(4-chlorophenyl)ethanedione, also known by its CAS number 88372-92-3, is an organic compound characterized by its structure, which features two 4-chlorophenyl groups attached to a central ethanedione moiety. This compound typically exhibits a solid state at room temperature and is known for its potential applications in organic synthesis and as a building block in the development of various chemical products. The presence of chlorine substituents on the phenyl rings enhances its reactivity and may influence its solubility in organic solvents. Bis(4-chlorophenyl)ethanedione can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions, making it a valuable intermediate in the synthesis of pharmaceuticals and agrochemicals. Additionally, its electronic properties may be of interest in materials science, particularly in the development of organic electronic devices. Safety data should be consulted for handling and storage, as with many chlorinated compounds, it may pose environmental and health risks.

Formula: C₁₄H₈Cl₂O₂

InChI: InChI=1/C14H8Cl2O2/c15-11-5-1-9(2-6-11)13(17)14(18)10-3-7-12(16)8-4-10/h1-8H

SMILES: c1cc(ccc1C(=O)C(=O)c1ccc(cc1)Cl)Cl

Synonyms:

• 1,2-Bis(4-chlorophenyl)ethane-1,2-dione
• 1,2-Ethanedione, 1,2-bis(4-chlorophenyl)-
• Benzil, 4,4'-dichloro-
• Bis(p-chlorophenyl)ethanedione
• Ethanedione, bis(4-chlorophenyl)-
• Ethanedione, bis(4-chlorophenyl)-,radical ion(1-)
• 4,4'-Dichlorobenzil