| Weight | 165.963 g/mol |
|---|---|
| Formula | C4HCl2NO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Dichloromaleimide (1193-54-0)
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- Organic chemistry in thionyl chloride. I. Dichloromaleimide chemistry. II. Thionyl chloride-pyridine method for the conversion of maleimides to dichloromaleimides (Journal of Organic Chemistry, 1972)
- Dichloromaleimide chemistry. III. Reaction of N-aryldichloromaleimide with phenols. Preparation and mass spectral rearrangements of N-aryl-3-aryloxy-4-chloromaleimides and N-aryl-3,4-bis(aryloxy)maleimides (Journal of Organic Chemistry, 1972)
- Synthesis and Fungicidal Activity of Isoxazolines Fused to 3,5-Dichloromaleimide (Collection of Czechoslovak Chemical Communications, 1992)
- Dichloromaleimide chemistry. I. Substituent effects on carbon-13 nuclear magnetic resonance and mass spectra (Journal of Organic Chemistry, 1972)
- Dichloromaleimide chemistry. IV. Preparation of poly(maleimideethers) from the reaction of bisdichloromaleimides with bisphenols (Journal of Polymer Science Part A, 1973)
- Studies on new cyclic imides obtained from aminophenazone with analgesic properties. Potent effects of a 3,4-dichloromaleimide derivative. (Drug Research, 2011)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1(=C(C(=O)NC1=O)Cl)Cl
-
InChIKeyKVBAKSQRUXXHCK-UHFFFAOYSA-N
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