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  2. Dimethoxymethane - Wikipedia

    en.wikipedia.org/wiki/Dimethoxymethane

    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 .

  3. Prices of chemical elements - Wikipedia

    en.wikipedia.org/wiki/Prices_of_chemical_elements

    This is a list of prices of chemical elements. Listed here are mainly average market prices for bulk trade of commodities. Listed here are mainly average market prices for bulk trade of commodities. Data on elements' abundance in Earth's crust is added for comparison.

  4. Dimethyl ether - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_ether

    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).

  5. Dimethoxyethane - Wikipedia

    en.wikipedia.org/wiki/Dimethoxyethane

    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.

  6. Chloromethyl methyl ether - Wikipedia

    en.wikipedia.org/wiki/Chloromethyl_methyl_ether

    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.

  7. Dimethyl malonate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_malonate

    Dimethyl malonate is a diester derivative of malonic acid.It is a common reagent for organic synthesis used, for example, as a precursor for barbituric acid.It is also used in the malonic ester synthesis.

  8. Pictet–Spengler reaction - Wikipedia

    en.wikipedia.org/wiki/Pictet–Spengler_reaction

    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]

  9. Diglyme - Wikipedia

    en.wikipedia.org/wiki/Diglyme

    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.