1,2,5,6-Tetrachloronaphthalene is a chlorinated aromatic compound characterized by the presence of four chlorine atoms attached to a naphthalene ring. This compound typically appears as a colorless to pale yellow solid and is known for its high stability and low volatility. It is insoluble in water but soluble in organic solvents, which makes it useful in various industrial applications, including as a chemical intermediate and in the production of specialty chemicals. The presence of multiple chlorine atoms enhances its hydrophobic properties and contributes to its potential environmental persistence. Toxicological studies indicate that exposure to this compound may pose health risks, including potential carcinogenic effects, necessitating careful handling and regulation. Additionally, it is important to note that 1,2,5,6-tetrachloronaphthalene can undergo various chemical reactions, such as substitution and reduction, which can be relevant in both synthetic chemistry and environmental degradation processes. Overall, its unique structure and properties make it a compound of interest in both industrial applications and environmental studies.

1,2,5,6-tetrachloronaphthalene

67922-22-9: 1,2,5,6-Tetrachloronaphthalene is a chlorinated aromatic compound characterized by the presence of four chlorine atoms attached to a naphthalene ring. This compound typically appears as a colorless to pale yellow solid and is known for its high stability and low volatility. It is insoluble in water but soluble in organic solvents, which makes it useful in various industrial applications, including as a chemical intermediate and in the production of specialty chemicals. The presence of multiple chlorine atoms enhances its hydrophobic properties and contributes to its potential environmental persistence. Toxicological studies indicate that exposure to this compound may pose health risks, including potential carcinogenic effects, necessitating careful handling and regulation. Additionally, it is important to note that 1,2,5,6-tetrachloronaphthalene can undergo various chemical reactions, such as substitution and reduction, which can be relevant in both synthetic chemistry and environmental degradation processes. Overall, its unique structure and properties make it a compound of interest in both industrial applications and environmental studies.

<p>Applications 1,2,5,6-Tetrachloronaphthalene is a polychlorinated naphthalene (PCN) with dioxin-like toxic properties. It can induce different biochemical changes by activating cellular aryl hydrocarbon receptor (AhR).<br>References Olivero-Verbel, J., et al.: J. Mol. Struc-Theochem., 678, 157 (2004)<br></p>

CAS 67922-22-9

1,2,5,6-tetrachloronaphthalene

1,2,5,6-Tetrachloronaphthalene

Ref: TR-T291545