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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). The simplest ether , it is a colorless gas that is a useful precursor to other organic compounds and an aerosol propellant that is currently being demonstrated for ...
Oxidation with dioxiranes refers to the introduction of oxygen into organic substrates using dioxiranes. Dioxiranes are well known for epoxidations (synthesis of epoxides from alkenes ). [ 1 ] Dioxiranes oxidize other unsaturated functionality, heteroatoms, and alkane C-H bonds. [ 2 ]
Diethyl ether hydroperoxide forms polymers known as diethyl ether peroxide, or ethylidene peroxide: The peroxide is a colorless oil that is an extremely brisant and friction sensitive explosive material , however the polymeric materials are solid making them more dangerous as evaporation of the volatile diethyl ether can leave thin films of ...
Dimethyl ether: A colourless gas that is used as an aerosol spray propellant. A potential renewable alternative fuel for diesel engines with a cetane rating as high as 56–57. Diethyl ether: A colourless liquid with sweet odour. A common low boiling solvent (b.p. 34.6 °C) and an early anaesthetic. Used as starting fluid for diesel engines.
Diglyme, or bis(2-methoxyethyl) ether, is an organic compound with the chemical formula (CH 3 OCH 2 CH 2) 2 O. It is a colorless liquid with a slight ether-like odor. It is a solvent with a high boiling point. It is the dimethyl ether of diethylene glycol. The name diglyme is a portmanteau of diglycol methyl ether. It is miscible with water as ...
The Rubottom oxidation is a ... Rubottom oxidation of the cyclic silyl enol ether under ... controlled stereoselective Rubottom oxidation using dimethyl ...
Some sulfides are named by modifying the common name for the corresponding ether. For example, C 6 H 5 SCH 3 is methyl phenyl sulfide, but is more commonly called thioanisole, since its structure is related to that for anisole, C 6 H 5 OCH 3. The modern systematic nomenclature in chemistry for the trival name thioether is sulfane. [2]
A generic epoxide. In organic chemistry, an epoxide is a cyclic ether, where the ether forms a three-atom ring: two atoms of carbon and one atom of oxygen.This triangular structure has substantial ring strain, making epoxides highly reactive, more so than other ethers.