| Weight | 152.964 g/mol |
|---|---|
| Formula | C4H2Cl2O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 2 |
FUMARYL CHLORIDE (627-63-4)
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- Solvent-free synthesis of penta-substituted pyrroles: one-pot reaction of amine, alkyl acetoacetate, and fumaryl chloride (Tetrahedron, 2009)
- Dynamics of Cl (2Pj) atom formation in the photodissociation of fumaryl chloride (ClCO - CH = CH - COCl) at 235 nm: a resonance enhanced multiphoton ionization (REMPI) time-of-flight (TOF) study. (Journal of Physical Chemistry A, 2011)
- DielsAlder reaction of furan and fumaryl chloride: X-ray crystal and molecular structure of an oxabicyclo[2.2.1]heptane derivative. Synthesis of reduction products of cis-maneonene-A (Journal of The Chemical Society, Chemical Communications, 1979)
- The vibrational assignment and crystal structure of fumaryl chloride (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1984)
- A spectroscopic study of the rotational equilibria in fumaryl chloride, fumaryl fluoride and maleoyl fluoride (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 1971)
- UV-laser photoisomerization of fumaryl chloride: The first identification of maleoyl chloride: matrix isolation infrared and ab initio studies (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2000)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(=CC(=O)Cl)C(=O)Cl
-
InChIKeyZLYYJUJDFKGVKB-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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FUMARYL CHLORIDE
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