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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.
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. [4] [5]
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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.
This page was last edited on 2 December 2017, at 03:38 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.
Dimethylethanolamine (DMAE or DMEA) is an organic compound with the formula (CH 3) 2 NCH 2 CH 2 OH.It is bifunctional, containing both a tertiary amine and primary alcohol functional groups.