| Weight | 140.953 g/mol |
|---|---|
| Formula | C3H2Cl2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
Malonyl chloride (1663-67-8)
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- Alpha,alpha'-annulation of 2,6-prenyl-substituted cyclohexanone derivatives with malonyl chloride: application to a short synthesis of (+/-)-clusianone. Formation and rearrangement of a biogenetic-like intermediate. (Organic Letters, 2007)
- 709. Heterocyclic syntheses with malonyl chloride. Part VI. 3-Substituted pyridine derivatives from -methylene-nitriles (Journal of The Chemical Society (resumed), 1962)
- Reaction of acylketene S,N-acetals with malonyl chloride: synthesis of novel 1,5-substituted 4-hydroxy-6-methylthio-2(1H)-pyridones and 6,8-substituted 4-hydroxy-7-methylthio-2,5-dioxo-5,6-dihydro-2H-pyrano[3,2-c]pyridines (Synthesis, 1988)
- Base-switched annuloselectivity in the reactions of ethyl malonyl chloride and imines (Organic and Biomolecular Chemistry, 2014)
- Heterocyclic syntheses with malonyl chloride. 15. 7Chloro3,4dihydro4,5dioxo3aryl(oralkyl)2thio2H,5Hpyrano[3,42e]1,3oxazine from aryl or alkyl isothiocyanates and their degradation with morpholine and ethanol (Journal Fur Praktische Chemie-chemiker-zeitung, 1988)
- Reverse osmotic properties of the membranes prepared from the polycondensate of 2,5-pyridinedicarboxylic acid chloride and malonyl dihydrazide (Polymer Bulletin, 1986)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C(=O)Cl)C(=O)Cl
-
InChIKeySXYFKXOFMCIXQW-UHFFFAOYSA-N
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