1,4-Bis(trichloromethyl)benzene

Chemical compound From Wikipedia, the free encyclopedia

1,4-Bis(trichloromethyl)benzene is an organic compound with the formula C6H4(CCl3)2. A white solid, it is prepared industrially by chlorination of para-xylene. It reacts with terephthalic acid to give terephthaloyl chloride, a precursor to Kevlar.[1] It also reacts with sulfur dioxide to give the same acid chloride and thionyl chloride.[2] It reacts with hydrogen fluoride in 1,2-dichloroethane to form 1,4-bis(chlorodifluoromethyl)benzene in a yield of 79%.[3]

Quick facts Names, Identifiers ...
1,4-Bis(trichloromethyl)benzene
Names
Preferred IUPAC name
1,4-Bis(trichloromethyl)benzene
Other names
hexachloroxylene; hexachloroparaxylene; Chloxil; Chloxyl
Identifiers
3D model (JSmol)
ChEMBL
ChemSpider
ECHA InfoCard 100.000.624 Edit this at Wikidata
EC Number
  • 200-686-3
UNII
  • InChI=1S/C8H4Cl6/c9-7(10,11)5-1-2-6(4-3-5)8(12,13)14/h1-4H
    Key: OTEKOJQFKOIXMU-UHFFFAOYSA-N
  • C1=CC(=CC=C1C(Cl)(Cl)Cl)C(Cl)(Cl)Cl
Properties
Appearance white solid
Density 1.778 g/cm3
Melting point 108–110 Â°C (226–230 Â°F; 381–383 K)
Boiling point 213 Â°C (415 Â°F; 486 K)
Hazards
GHS labelling:
GHS05: CorrosiveGHS06: Toxic
Danger
H301, H311, H314, H331
P260, P264, P270, P271, P280, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P310, P311, P312, P321, P322, P330, P361, P363, P403+P233, P405, P501
Except where otherwise noted, data are given for materials in their standard state (at 25 Â°C [77 Â°F], 100 kPa).
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