Trichloroacetyl chloride
Chemical compound / From Wikipedia, the free encyclopedia
Trichloroacetyl chloride is the acyl chloride of trichloroacetic acid. It can be formed by reacting chlorine with acetyl chloride or acetaldehyde in the presence of activated charcoal. It is used in the manufacture of pharmaceuticals and plant protection compounds.[4]
Quick Facts Names, Identifiers ...
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Names | |||
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Preferred IUPAC name
Trichloroacetyl chloride | |||
Other names
2,2,2-Trichloroacetyl chloride | |||
Identifiers | |||
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3D model (JSmol) |
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ChemSpider |
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ECHA InfoCard | 100.000.843 | ||
EC Number |
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PubChem CID |
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UNII | |||
UN number | 2442 | ||
CompTox Dashboard (EPA) |
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Properties | |||
C2Cl4O | |||
Molar mass | 181.832 g/mol | ||
Density | 1.62 g/cm3 at 20 °C | ||
Boiling point | 117.9 °C (244.2 °F; 391.0 K) | ||
Solubility | miscible with diethyl ether[1] | ||
Thermochemistry | |||
Std enthalpy of formation (ΔfH⦵298) |
-280.0 kJ•mol−1[2] | ||
Hazards | |||
GHS labelling:[3] | |||
Danger | |||
H302, H314, H330 | |||
P260, P264, P270, P271, P280, P284, P301+P312, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P320, P330, P363, P403+P233, P405 | |||
Safety data sheet (SDS) | Oxford MSDS | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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