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It is employed as emollients, masking agents, plasticisers and solvents.
Tejraj M. Aminabhavi.; Hemant T. S. Phayde.; Rajashekhar S. Khinnavar.; Bindu Gopalakrishna.; Keith C. Hansen. Densities, refractive indices, speeds of sound, and shear viscosities of diethylene glycol dimethyl ether with ethyl acetate, methyl benzoate, ethyl benzoate, and diethyl succinate in the temperature range from 298.15 to 318.15 K.J. Chem. Eng. Data. 1994, 39 (2),251-260 .
Niki M. Zacharias.; Henry R. Chan.; Napapon Sailasuta.; Brian D. Ross.; Pratip Bhattacharya. Real-Time Molecular Imaging of Tricarboxylic Acid Cycle Metabolism in Vivo by Hyperpolarized 1-13C Diethyl Succinate.J. Am. Chem. Soc. 2012, 134 (2),934-943 .
Undergoes the Stobbe condensation with carbonyl compounds to give alkylidene derivatives; review: Org. React., 6, 1 (1951). For the Stobbe condensation with benzophenone to give the monoester of the product, see: Org. Synth. Coll., 4, 132 (1963).
For an example of the acyloin condensation under silylating conditions to give 2-hydroxycyclobutanone, see: Org. Synth. Coll., 6, 167 (1988). An alternative work-up with bromine leads directly to 1,2-cyclobutanedione: Org. Synth. Coll., 7, 112 (1990):
Gefahrenhinweise (EU): H227
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