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Dimethoxymethane, also called methylal, is a colorless flammable liquid with a low boiling point, low viscosity and excellent dissolving power. It has a chloroform-like odor and a pungent taste. It is the dimethyl acetal of formaldehyde. Dimethoxymethane is soluble in three parts water [clarification needed] and miscible with most common ...
Dimethyl ether (DME; also known as methoxymethane) is the organic compound with the formula CH 3 OCH 3, (sometimes ambiguously simplified to C 2 H 6 O as it is an isomer of ethanol).
Structure of the coordination complex NbCl 3 (dimethoxyethane)(3-hexyne). [5]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.
Chloromethyl methyl ether (CMME) is a compound with formula CH 3 OCH 2 Cl. A colorless liquid, it is a chloroalkyl ether.It is used as an alkylating agent.In organic synthesis, it is used for introducing the methoxymethyl ether (MOM) protecting group, [3] and is thus often called MOM-Cl or MOM chloride.
Reverso is a French company specialized in AI-based language tools, translation aids, and language services. [2] These include online translation based on neural machine translation (NMT), contextual dictionaries, online bilingual concordances, grammar and spell checking and conjugation tools.
Polyoxymethylene dimethyl ethers (PODE or DMMn) are a class of chemical compounds with the molecular formula H 3 CO(CH 2 O) n CH 3 where n is typically about 3 to 8.. PODE can be produced from methylal and formaldehyde or a formaldehyde equivalent such as paraformaldehyde [1] or trioxane.
In organic chemistry, a methoxymethyl ether is a functional group with the formula ROCH 2 OCH 3, abbreviated MOM.It is a kind of chloroalkyl ether and, like its congeners, often employed in organic synthesis to protect alcohols.
The original Pictet–Spengler reaction was the reaction of phenethylamine and dimethoxymethane, catalysed by hydrochloric acid forming a tetrahydroisoquinoline. The Pictet–Spengler reaction has been applied to solid-phase combinatorial chemistry with great success.