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Diethylsuccinoylsuccinate is an organic compound with the formula [CH 2 C(OH)=C(CO 2 Et)] 2 (Et = ethyl). A tetrasubstituted derivative of 1,4-cyclohexadiene, the compound is the enol tautomer of the corresponding cyclohexadione. [1] It is produced by base-induced condensation of diethyl succinate: [2] 2 EtO 2 CCH 2 CH 2 CO 2 Et [CH 2 C(OH)=C ...
Download as PDF; Printable version; ... 2.79 6.55 –20.2 Diethyl ether: 0.713 34.5 2.16 –116.3 ... [2] K b [1] Water: 100.00 0.512 0.00
CH 3 CO 2 H: acetic acid: 64-19-7 (CH 3) 2 CO: acetone: 67-64-1 CH 3 CN: acetonitrile: 75-05-8 CH 3 CH 2 CH(OH)CH 2 OH: 1,2-Butanediol: 584-03-2 CH 3 CH(OH)CH 2 CH 2 OH: 1,3-Butanediol: 107-88-0 HOCH 2 CH 2 CH 2 CH 2 OH: 1,4-Butanediol: 110-63-4 C 6 H 14 O 2: 2-Butoxyethanol: 111-76-2 CH 3 CH 2 CH 2 COOH: butyric acid: 107-92-6 HN(CH 2 CH 2 OH ...
The following chart shows the solubility of various ionic compounds in water at 1 atm pressure and room temperature (approx. 25 °C, 298.15 K). "Soluble" means the ionic compound doesn't precipitate, while "slightly soluble" and "insoluble" mean that a solid will precipitate; "slightly soluble" compounds like calcium sulfate may require heat to precipitate.
This page contains tables of azeotrope data for various binary and ternary mixtures of solvents. The data include the composition of a mixture by weight (in binary azeotropes, when only one fraction is given, it is the fraction of the second component), the boiling point (b.p.) of a component, the boiling point of a mixture, and the specific gravity of the mixture.
Diethyl sulfate (DES) is an organosulfur compound with the formula (C 2 H 5) 2 SO 4. [1] [2] It occurs as a colorless, oily liquid with a faint peppermint odor. It is toxic, combustible, and likely carcinogenic chemical compound. [3] [2] Diethyl sulfate is used as an ethylating agent.
These uses exploit its basicity. Diethyl ether is a popular non-polar solvent in liquid-liquid extraction. As an extractant, it is immiscible with and less dense than water. Although immiscible, it has significant solubility in water (6.05 g/(100 ml) at 25 °C [2]) and dissolves 1.5 g/(100 g) (1.0 g/(100 ml)) water at 25 °C. [13]
The Sharpless epoxidation is viable with a large range of primary and secondary alkenic alcohols. Furthermore, with the exception noted above, a given dialkyl tartrate will preferentially add to the same face independent of the substitution on the alkene.To demonstrate the synthetic utility of the Sharpless epoxidation, the Sharpless group created synthetic intermediates of various natural ...