enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Acetylpropionyl - Wikipedia

    en.wikipedia.org/wiki/Acetylpropionyl

    Acetylpropionyl, also known as acetyl propionyl or 2,3-pentanedione, [1] is an organic compound, specifically a diketone. [2] Uses for acetylpropionyl include as a: Solvent for cellulose acetate, paints, inks, and lacquers; Starting material for dyes, pesticides, and drugs

  3. 2,3,4-Pentanetrione - Wikipedia

    en.wikipedia.org/wiki/2,3,4-Pentanetrione

    2,3,4-Pentanetrione (or IUPAC name pentane-2,3,4-trione, triketopentane or dimethyl triketone) is the simplest linear triketone, a ketone with three C=O groups. It is an organic molecule with formula CH 3 COCOCOCH 3 .

  4. 2,4-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,4-Dimethylpentane

    2,4-Dimethylpentane is an alkane with the chemical formula [(H 3 C) 2 CH] 2 CH 2. This colorless hydrocarbon is produced in large quantities in oil refineries. It results from the alkylation of isobutane by propylene. [1] Often referred to as "alkylate", it is blended with other gasoline components to give a high octane fuel.

  5. 2-Methyl-2,4-pentanediol - Wikipedia

    en.wikipedia.org/wiki/2-Methyl-2,4-pentanediol

    2-Methyl-2,4-pentanediol (MPD) is an organic compound with the formula (CH 3) 2 C(OH)CH 2 CH(OH)CH 3. This colourless liquid is a chiral diol . It is produced industrially from diacetone alcohol by hydrogenation . [ 4 ]

  6. 2,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/2,3-Dimethylpentane

    9 – MgBr with acetone to form 2,3-dimethyl-2-pentanol, then dehydrating this alcohol to form 2,3-dimethyl-2-pentene, and hydrogenating this product. [ 4 ] The isomer is present at about 2.4% by weight in the hydrocarbon mixture obtained by the condensation of methanol at 200 °C with a zinc iodide catalyst (the main component of the mixture ...

  7. Knorr pyrrole synthesis - Wikipedia

    en.wikipedia.org/wiki/Knorr_pyrrole_synthesis

    Levi and Zanetti extended the Knorr synthesis in 1894 to the use of acetylacetone (2,4-pentanedione) in reaction with ethyl 2-oximinoacetoacetate. The result was ethyl 4-acetyl-3,5-dimethylpyrrole-2-carboxylate, where "OEt" = R 1 = R 3 = Me, and R 2 = COOEt. [9] The 4-acetyl group could easily be converted to a 4-ethyl group by Wolff-Kishner ...

  8. Roberts warns against ignoring Supreme Court rulings as ...

    www.aol.com/roberts-warns-against-ignoring...

    Supreme Court Chief Justice John Roberts slammed what he described as “dangerous” talk by some officials about ignoring federal court rulings, using an annual report weeks before President ...

  9. 3,3-Dimethylpentane - Wikipedia

    en.wikipedia.org/wiki/3,3-Dimethylpentane

    In 1929 Graham Edgar and George Calingaert made 3,3-dimethylpentane and measured its physical characteristics for the first time. The measurements were at 20 °C, not the standard conditions used in later times. [3] For 3,3-dimethylpentane they measured a density of 0.6934 at 20 °C with a rate of change Δd/ΔT of 0.000848.