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Ethyl cyanoacetate is an organic compound that contains a carboxylate ester and a nitrile. It is a colourless [ 1 ] liquid with a pleasant odor. This material is useful as a starting material for synthesis due to its variety of functional groups and chemical reactivity.
In its largest scale application, cyanoacetic acid is first esterified to give ethyl cyanoacetate. Condensation of that ester with formaldehyde gives ethyl cyanoacrylate , which used as superglue. As of 2007, more than 10,000 tons of cyanoacetic acid were produced annually.
Methoxypropylamino cyclohexenylidene ethoxyethylcyanoacetate is an organic compound used in sunscreens to absorb UVA radiation.It is marketed as Mexoryl 400 by L'Oréal. ...
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Ethyl cyanoacrylate (ECA), a cyanoacrylate ester, is an ethyl ester of 2-cyano-acrylic acid. It is a colorless liquid with low viscosity and a faint sweet smell in pure form. It is the main component of cyanoacrylate glues and can be encountered under many trade names . [ 2 ]
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The following other wikis use this file: Usage on de.wikipedia.org Cyanessigsäureethylester; Usage on fi.wikipedia.org Käyttäjä:Nitraus/A; Etyylisyanoasetaatti; Usage on fr.wikipedia.org Cyanoacétate d'éthyle; Usage on ja.wikipedia.org シアノ酢酸エチル; Usage on www.wikidata.org Q1146961; Usage on zh.wikipedia.org
Cyanoethylation is a process for the attachment of CH 2 CH 2 CN group to another organic substrate. The method is used in the synthesis of organic compounds. [1]Cyanoethylation entails addition of protic nucleophiles to acrylonitrile.