enow.com Web Search

Search results

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

    en.wikipedia.org/wiki/Methyl_propiolate

    Density: 0.945 g mL −1: Boiling point: 103–105 °C (217–221 °F; 376–378 K) ... Methyl propiolate is an organic compound with the formula HC 2 CO 2 CH 3.

  3. Propiolic acid - Wikipedia

    en.wikipedia.org/wiki/Propiolic_acid

    Density: 1.1325 g/cm 3: Melting point: 9 °C (48 °F; 282 K) Boiling point: ... Common examples include methyl propiolate and ethyl propiolate. See also. Propargyl;

  4. Category:Methyl esters - Wikipedia

    en.wikipedia.org/wiki/Category:Methyl_esters

    Pages in category "Methyl esters" The following 200 pages are in this category, out of approximately 303 total. ... Methyl propiolate; Methyl propionate; Methyl ...

  5. Dimethyl acetylenedicarboxylate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_acetylenedi...

    Properties Chemical formula. C 6 H 6 O 4 Molar mass: 142.11 g/mol Appearance Colorless liquid Density: 1.1564 g/cm 3: ... Methyl propiolate, Hexafluoro-2-butyne ...

  6. Methyl propionate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propionate

    Methyl propionate, also known as methyl propanoate, is an organic compound with the molecular formula CH 3 CH 2 CO 2 CH 3. It is a colorless liquid with a fruity, rum -like odor. [ 2 ]

  7. C4H4O2 - Wikipedia

    en.wikipedia.org/wiki/C4H4O2

    Methyl propiolate; Tetrolic acid This page was last edited on 1 October 2024, at 00:31 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...

  8. N-Methylmorpholine - Wikipedia

    en.wikipedia.org/wiki/N-Methylmorpholine

    N-Methylmorpholine is the organic compound with the formula O(CH 2 CH 2) 2 NCH 3.It is a colorless liquid. It is a cyclic tertiary amine.It is used as a base catalyst for generation of polyurethanes and other reactions.

  9. Bismuthinidene - Wikipedia

    en.wikipedia.org/wiki/Bismuthinidene

    A similar cycloaddition reaction between Dostál's bismuthinidene and methyl propiolate yields an iminonaphthalene only as an intermediate, as the bridgehead bismuth atom is quickly attacked by a deprotonated second equivalent of methyl propiolate, breaking the Bi-N bond and yielding a boat-shaped bismacyclohexadiene moiety. [29]