Weight | 181.833 g/mol |
---|---|
Formula | C2Cl4O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
TRICHLOROACETYL CHLORIDE (76-02-8)
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- A mild, high-yield conversion of aldoximes into nitriles using trichloroacetyl chloride/triethylamine (Synthesis, 1983)
- Conversion of carboxamides to nitriles using trichloroacetyl chloride/triethylamine as a mild dehydrating agent (Synthesis, 1985)
- The oxidation of triethylamine by trichloroacetyl chloride (Tetrahedron, 1969)
- Mutagenicity of dichloroacetylene and its degradation products trichloroacetyl chloride, trichloroacryloyl chloride and hexachlorobutadiene (Mutation Research\/genetic Toxicology, 1983)
- Heterogeneous chemistry of trichloroacetyl chloride in the atmosphere (Journal of Geophysical Research, 1994)
- Reactions of trichloroacetyl chloride with 2-picoline N-oxide and pyridylcarbinols (Journal of Organic Chemistry, 1968)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=O)(C(Cl)(Cl)Cl)Cl
-
InChIKeyPVFOMCVHYWHZJE-UHFFFAOYSA-N
- Pubchem - TRICHLOROACETYL CHLORIDE
- Wikipedia - trichloroacetyl chloride
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.
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1 alternate name
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3 suppliers
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(359-28-4)
1 alternate name
3 suppliers
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(79-30-1)
1 alternate name
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3 suppliers
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1 alternate name
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1 alternate name
3 suppliers
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1 alternate name
3 suppliers
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1 alternate name
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1 alternate name
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3 suppliers
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1 alternate name
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1 alternate name
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1 alternate name
3 suppliers
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3,3-Dimethylbutyryl chloride
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