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In the presence of oxygen, ethane-1,1-dithiol is converted to cis/trans-3,6-dimethyl-1,2,4,5-tetrathiane which has a rubbery aroma. This molecule has a ring with four sulfur atoms and two carbons, two ethane-1,1-dithiol molecules become linked at their sulfur atoms with the loss of hydrogen. [11]
Together with a high-permittivity solvent (e.g. propylene carbonate), dimethoxyethane is used as the low-viscosity component of the solvent for electrolytes of lithium batteries. In the laboratory, DME is used as a coordinating solvent. Dimethoxyethane is often used as a higher-boiling-point alternative to diethyl ether and tetrahydrofuran.
1,1-Diethoxyethane (acetaldehyde diethyl acetal) is a major flavoring component of distilled beverages, especially malt whisky [3] and sherry. [4] Although it is just one of many compounds containing an acetal functional group, this specific chemical is sometimes called simply acetal .
Phase behavior Triple point: 91 K (−182 °C), 1.1 Pa Critical point: 305.3 K (32.2 °C), 4.9 MPa Std enthalpy change of fusion, Δ fus H o: 9.76 kJ/mol at −182 °C
Ethylene glycol (IUPAC name: ethane-1,2-diol) is an organic compound (a vicinal diol [7]) with the formula (CH 2 OH) 2. It is mainly used for two purposes: as a raw material in the manufacture of polyester fibers and for antifreeze formulations. It is an odorless, colorless, flammable, viscous liquid.
2,2-Dichloro-1,1,1-trifluoroethane can be produced by reacting tetrachloroethylene with hydrogen fluoride in the gas phase. This is an exothermic reaction and requires a catalyst: This is an exothermic reaction and requires a catalyst:
Orthoacetic acid or ethane-1,1,1-triol is an hypothetical organic compound with formula C 2 H 6 O 3 or H 3 C-C(OH) 3. It would be an ortho acid with the ethane backbone. Orthoacetic acid is believed to be impossible to isolate, since it would readily decompose into acetic acid and water. It may have a fleeting existence in aqueous solutions of ...
1,1-Diethoxyethane; 1,2-Diethoxyethane [Wikidata] (ethylene glycol diethyl ether This page was last edited on 12 July 2024, at 14:02 (UTC). Text is available under ...