| Weight | 126.97 g/mol |
|---|---|
| Formula | C3H4Cl2O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
1,1-Dichloroacetone (30605-38-0, 513-88-2)
1,1-dichloropropanone · 1,1-dichloro-2-propanone
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- Kinetics of the reversible hydration of 1, 3-dichloroacetone in dioxan and acetonitrile solution (1968)
- REACTION ORDERS AND ISOTOPE EFFECTS IN THE REVERSIBLE ADDITION OF WATER TO 1,3-DICHLOROACETONE IN AQUEOUS DIOXAN. (1971)
- Indirect Electrooxidation of Halohydrins by a Double Mediatory System of Ru(VIII)/Ru(IV) and [Cl+]/Cl. Optimization for the Oxidation of 1,3-Dichloro-2-propanol to 1,3-Dichloroacetone (Bulletin of the Chemical Society of Japan, 1990)
- Substituted 1,3-Dichloroisopropanols, Cyclopropanols, and Ethyl Ketones from 1,3-Dichloroacetone (Synthesis, 1983)
- 1,3-dithiomesoxalamides - Crystal-structure and Synthesis From 1,3-dichloroacetone, Sulfur and Secondary-amines (Tetrahedron, 1985)
- Cyclic ketones via the reaction of dithiols with 1,3-dichloroacetone. An unexpected base-catalyzed rearrangement of .alpha.,.alpha.'-dithia ketones (Journal of Organic Chemistry, 1993)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 1,1-dichloropropanone
- 1,1-dichloro-2-propanone
-
SMILESCC(=O)C(Cl)Cl
-
InChIKeyCSVFWMMPUJDVKH-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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1,1-Dichloroacetone
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