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diethyl maleate
A maleate ester resulting from the formal condensation of both carboxy groups of maleic acid with ethanol. A colourless liquid at room temperature (m.p. -10degreeC) with boiling point 220degreeC at 1 atm., it is commonly used as a dienophile for Diels-Alder-type cycloaddition reactions in organic synthesis.


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03. Biological Effects of Specific Chemicals: glutathione depleting agent [CHEBI:68509] > diethyl maleate [CHEBI:68508]
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03. Biological Effects of Specific Chemicals 
03. Biological Effects of Specific Chemicals
 glutathione depleting agent [CHEBI:68509] (1) 
 diethyl maleate [CHEBI:68508] (1)
08. Chemical Category 
08. Chemical Category
 main group molecular entity [CHEBI:33579] (25650) 
 p-block molecular entity [CHEBI:33675] (25343) 
 chalcogen molecular entity [CHEBI:33304] (15225) 
 oxygen molecular entity [CHEBI:25806] (14414) 
 organooxygen compound [CHEBI:36963] (11352) 
 carbonyl compound [CHEBI:36586] (5928) 
 carboxylic ester [CHEBI:33308] (1495) 
 alpha,beta-unsaturated carboxylic ester [CHEBI:51737] (68) 
 enoate ester [CHEBI:51702] (65) 
 maleate ester [CHEBI:35486] (2) 
 diethyl maleate [CHEBI:68508] (1)
 organochalcogen compound [CHEBI:36962] (11874) 
 organooxygen compound [CHEBI:36963] (11352) 
 carbonyl compound [CHEBI:36586] (5928) 
 carboxylic ester [CHEBI:33308] (1495) 
 alpha,beta-unsaturated carboxylic ester [CHEBI:51737] (68) 
 enoate ester [CHEBI:51702] (65) 
 maleate ester [CHEBI:35486] (2) 
 diethyl maleate [CHEBI:68508] (1)
 carbon group molecular entity [CHEBI:33582] (23847) 
 organic molecular entity [CHEBI:50860] (23769) 
 heteroorganic entity [CHEBI:33285] (15197) 
 organochalcogen compound [CHEBI:36962] (11874) 
 organooxygen compound [CHEBI:36963] (11352) 
 carbonyl compound [CHEBI:36586] (5928) 
 carboxylic ester [CHEBI:33308] (1495) 
 alpha,beta-unsaturated carboxylic ester [CHEBI:51737] (68) 
 enoate ester [CHEBI:51702] (65) 
 maleate ester [CHEBI:35486] (2) 
 diethyl maleate [CHEBI:68508] (1)
 ester [CHEBI:35701] (3370) 
 carboxylic ester [CHEBI:33308] (1495) 
 alpha,beta-unsaturated carboxylic ester [CHEBI:51737] (68) 
 enoate ester [CHEBI:51702] (65) 
 maleate ester [CHEBI:35486] (2) 
 diethyl maleate [CHEBI:68508] (1)
 organic molecule [CHEBI:72695] (11399) 
 organic oxo compound [CHEBI:36587] (5932) 
 carbonyl compound [CHEBI:36586] (5928) 
 carboxylic ester [CHEBI:33308] (1495) 
 alpha,beta-unsaturated carboxylic ester [CHEBI:51737] (68) 
 enoate ester [CHEBI:51702] (65) 
 maleate ester [CHEBI:35486] (2) 
 diethyl maleate [CHEBI:68508] (1)
 polyatomic entity [CHEBI:36357] (18777) 
 molecule [CHEBI:25367] (11520) 
 organic molecule [CHEBI:72695] (11399) 
 organic oxo compound [CHEBI:36587] (5932) 
 carbonyl compound [CHEBI:36586] (5928) 
 carboxylic ester [CHEBI:33308] (1495) 
 alpha,beta-unsaturated carboxylic ester [CHEBI:51737] (68) 
 enoate ester [CHEBI:51702] (65) 
 maleate ester [CHEBI:35486] (2) 
 diethyl maleate [CHEBI:68508] (1)
ChEBI Compound Accession Identifier  [CHEBI:68508]
ChEBI Compound Description  A maleate ester resulting from the formal condensation of both carboxy groups of maleic acid with ethanol. A colourless liquid at room temperature (m.p. -10degreeC) with boiling point 220degreeC at 1 atm., it is commonly used as a dienophile for Diels-Alder-type cycloaddition reactions in organic synthesis.
ChEBI Compound Identification Number  68508
ChEBI InChI Value  InChI=1S/C8H12O4/c1-3-11-7(9)5-6-8(10)12-4-2/h5-6H,3-4H2,1-2H3/b6-5-
ChEBI InChIKey Value  IEPRKVQEAMIZSS-WAYWQWQTSA-N
ChEBI Compound Name  diethyl maleate
ChEBI SMILES Value  CCOC(=O)\\C=C/C(=O)OCC
ChEBI Substance ID  160645794
ChEBI URL  ChEBI:68508
ChemSpider ID  4436353
Ontomatica Chemical Accession Key (OnChAKey)  IEPRKVQEAMIZSS_WAYWQWQTSA_N_000_000000
PubChem Compound ID  5271566