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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 ...
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.
Diethyl succinate is the diethyl ester of succinate. It is a colorless liquid with the formula (CH 2 CO 2 Et) 2 (Et = ethyl). The organic molecule contains two ester groups. This ester is a versatile chemical intermediate. A colorless liquid, diethyl succinate is formed by Fischer esterification of succinic acid and ethanol.
The following compounds are liquid at room temperature and are completely miscible with water; ... (CH 2) 4 O: tetrahydrofuran: 109-99-9 C 6 H 14 O 4: triethylene ...
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]
1,4-Cyclohexanedione is an organic compound with the formula (CH 2) 4 (CO) 2. This white solid is one of the three isomeric cyclohexanediones . This particular diketone is used as a building block in the synthesis of more complex molecules.
Diethyl tartrate is an organic compound with the formula (HOCHCO 2 Et) 2 (Et = ethyl). Three stereoisomers exist, R,R-, S,S-, and R,S (=S,R-). They are the ethyl esters of the respective R,R-, S,S-, and R,S-tartaric acids. The R,R- and S,S- isomers are enantiomeric, being mirror images. The meso stereoisomer is not chiral. The chiral isomer is ...
Sodium diethyldithiocarbamate typically crystallizes from water as the trihydrate NaS 2 CN(C 2 H 5) 2. 3H 2 O. The anhydrous salt and the trihydrate are often used interchangeably. [1] Sodium diethyldithiocarbamate is obtained by treating carbon disulfide with diethylamine in the presence of sodium hydroxide: CS 2 + HN(C 2 H 5) 2 + NaOH → NaS ...