| Weight | 170.979 g/mol |
|---|---|
| Formula | C4H4Cl2O3 |
| Hydrogen Acceptors | 3 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Chloroacetic anhydride (541-88-8)
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- Use of chloroacetic anhydride for the protection of nucleoside hydroxyl groups. (Journal of Organic Chemistry, 1970)
- 297. Quantitative studies of the reactivities of mixed carboxylic anhydrides. Part I. The composition of the acylation products in the reaction between acetic chloroacetic anhydride and primary aromatic amines (Journal of The Chemical Society (resumed), 1950)
- CLXXIX.The interaction of bromine with acetic anhydride. Part V. Bromination and chlorination compared (continued). Some properties of acetic chloroacetic anhydride (Journal of The Chemical Society (resumed), 1929)
- Reaction of aliphatic isocyanides with chloroacetic anhydride and trifluoroacetic anhydride (Collection of Czechoslovak Chemical Communications, 1972)
- 298. Quantitative studies of the reactivities of mixed carboxylic anhydrides. Part II. The determination of some reaction velocities involving acetic chloroacetic anhydride (Journal of The Chemical Society (resumed), 1950)
- Tri:chloroacetic anhydride prodn. - by heating penta:chloroethyl tri:chloroacetate and tri:chloroacetic acid, opt. with amine or phosphine catalyst (1981)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C(=O)OC(=O)CCl)Cl
-
InChIKeyPNVPNXKRAUBJGW-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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