Tetrachloro-m-xylene
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Names | |||
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Preferred IUPAC name
1,2,3,5-Tetrachloro-4,6-dimethylbenzene | |||
Other names
Tetrachlorometaxylene
2,4,5,6-Tetrachlorometaxylene | |||
Identifiers | |||
3D model (
JSmol ) |
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Abbreviations | TCMX | ||
ChemSpider | |||
ECHA InfoCard
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100.011.715 | ||
EC Number |
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PubChem CID
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
C8H6Cl4 | |||
Molar mass | 243.94524 | ||
Appearance | colorless or white solid | ||
Melting point | 223 °C (433 °F; 496 K) | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tetrachloro-m-xylene (tetrachlorometaxylene, or TCMX) is the
ferric chloride-catalyzed reaction of the xylene with chlorine.[1]
TCMX is used as an
References
- ^ Riegger, Paul; Steffen, Klaus Dieter (1979). "Chlorination of xylenes and secondary Products. I. Chlorination of the nucleus and Side Chains of Xylenes". Chemiker-Zeitung. 103: 1-7.
- ^ Organochlorine Pesticides by GCxGC-ECD[permanent dead link]
- PMID 17933606.