| Weight | 169.18 g/mol |
|---|---|
| Formula | C8H11NO3 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 4 |
Ethyl (ethoxymethylene)cyanoacetate (94-05-3, 42466-67-1)
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- Cyclisierungsreaktionen zu Pyrano[3,2-c]pyridinen und pyrano[3,2-c]chinolinen unter Verwendung von Ethoxymethylen-malodinitril bzw.-cyanessigester Synthesen mit Nitrilen, 50. Mitt. pyrano[3,2-c]quinolines with ethoxymethylene-malonitrile and-ethyl cyanoacetate, resp. (Monatshefte Fur Chemie, 1978)
- Structural and theoretical evidence of the reaction products of ethyl(ethoxymethylene)cyanoacetate with 5-phenoxymethyl-2-amino-2-oxazoline (Journal of Molecular Structure, 1999)
- Systemic contact allergy from occupational contact with ethyl ethoxymethylene cyanoacetate. (Contact Dermatitis, 1992)
- Copper Iodide Mediated Cyanation of Arylboronic Acids and Aryl Iodides with Ethyl (Ethoxymethylene)cyanoacetate as Cyanating Agent (Synlett, 2016)
- ChemInform Abstract: Copper Iodide Mediated Cyanation of Arylboronic Acids and Aryl Iodides with Ethyl (Ethoxymethylene)cyanoacetate as Cyanating Agent. (ChemInform, 2016)
- Copper-mediated CH cyanation of (hetero)arenes with ethyl (ethoxymethylene)cyanoacetate as a cyanating agent (Chemical Communications, 2017)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCCOC=C(C#N)C(=O)OCC
-
InChIKeyKTMGNAIGXYODKQ-UHFFFAOYSA-N
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Synthesis
Reactant
+
Chloroethane
(Williamson ether)
Reactant
+
1-Hydroxy-1,2-benziodoxol-3(1H)-one 1-oxide
(Nicolaou IBX dehydrogenation)
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Ethyl (ethoxymethylene)cyanoacetate
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