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  2. 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, ...

  3. Methyl propiolate - Wikipedia

    en.wikipedia.org/wiki/Methyl_propiolate

    It is the methyl ester of propiolic acid, the simplest acetylenic carboxylic acid. It is a colorless liquid that is miscible with organic solvents. The compound is a reagent and building block for the synthesis of other organic compounds, reactions that exploit the electrophilicity of the alkyne group. [1] For example it is a potent dienophile. [2]

  4. Methyl methacrylate - Wikipedia

    en.wikipedia.org/wiki/Methyl_methacrylate

    The first stage involves carboalkoxylation of ethylene to produce methyl propionate (MeP): [12] C 2 H 4 + CO + CH 3 OH → CH 3 CH 2 CO 2 CH 3. The MeP synthesis is conducted in a continuous-stirred tank reactor at moderate temperature and pressure using proprietary agitation and gas-liquid mixing arrangement.

  5. Carbonylation - Wikipedia

    en.wikipedia.org/wiki/Carbonylation

    Synthesis of acrylic acid using "Reppe chemistry"; a metal catalyst is required. The carbomethoxylation of ethylene to give methyl propionate: C 2 H 4 + CO + MeOH → MeO 2 CC 2 H 5. Methyl propionate ester is a precursor to methyl methacrylate. [10] Hydroesterification is like hydrocarboxylation, but it uses alcohols in place of water. [11]

  6. Propionic acid - Wikipedia

    en.wikipedia.org/wiki/Propionic_acid

    The propionate / ˈ p r oʊ p i ə n eɪ t /, or propanoate, ion is C 2 H 5 COO −, the conjugate base of propionic acid. It is the form found in biological systems at physiological pH. A propionic, or propanoic, compound is a carboxylate salt or ester of propionic acid. In these compounds, propionate is often written in shorthand, as CH 3 CH ...

  7. Propionyl-CoA - Wikipedia

    en.wikipedia.org/wiki/Propionyl-CoA

    Propionyl-CoA is a coenzyme A derivative of propionic acid.It is composed of a 24 total carbon chain (without the coenzyme, it is a 3 carbon structure) and its production and metabolic fate depend on which organism it is present in. [1] Several different pathways can lead to its production, such as through the catabolism of specific amino acids or the oxidation of odd-chain fatty acids. [2]

  8. Isobutyl acetate - Wikipedia

    en.wikipedia.org/wiki/Isobutyl_acetate

    The chemical compound isobutyl acetate, also known as 2-methylpropyl ethanoate (IUPAC name) or β-methylpropyl acetate, is a common solvent.It is produced from the esterification of isobutanol with acetic acid.

  9. Robinson annulation - Wikipedia

    en.wikipedia.org/wiki/Robinson_annulation

    The Wieland–Miescher ketone is the Robinson annulation product of 2-methyl-cyclohexane-1,3-dione and methyl vinyl ketone. This compound is used in the syntheses of many steroids possessing important biological properties and can be made enantiopure using proline catalysis.