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  2. Isopropenyl acetate - Wikipedia

    en.wikipedia.org/wiki/Isopropenyl_acetate

    Isopropenyl acetate is an organic compound, which is the acetate ester of the enol tautomer of acetone. This colorless liquid is significant commercially as the ...

  3. Propenyl - Wikipedia

    en.wikipedia.org/wiki/Propenyl

    In organic chemistry, 1-propenyl (or simply propenyl) has the formula CH=CHCH 3 and 2-propenyl (isopropenyl) ... Isopropenyl acetate is a 2-propenyl ester, ...

  4. List of UN numbers 2401 to 2500 - Wikipedia

    en.wikipedia.org/wiki/List_of_UN_numbers_2401_to...

    UN Number Class Proper Shipping Name UN 2401: 8: Piperidine: UN 2402: 3: Propanethiols: UN 2403: 3: Isopropenyl acetate: UN 2404: 3: Propionitrile: UN 2405: 3 ...

  5. Isopropyl acetate - Wikipedia

    en.wikipedia.org/wiki/Isopropyl_acetate

    Isopropyl acetate is a solvent with a wide variety of manufacturing uses that is miscible with most other organic solvents, and slightly soluble in water (although less so than ethyl acetate). It is used as a solvent for cellulose, plastics, oil and fats. It is a component of some printing inks [4] and perfumes.

  6. Category:Isopropenyl esters - Wikipedia

    en.wikipedia.org/wiki/Category:Isopropenyl_esters

    Isopropenyl acetate This page was last edited on 12 December 2022, at 05:27 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4.0 ...

  7. Meerwein arylation - Wikipedia

    en.wikipedia.org/wiki/Meerwein_arylation

    In a novel kilogram-scale metal-free Meerwein arylation the diazonium salt is formed from 2-nitroaniline, the alkene isopropenyl acetate is an adduct of propyne and acetic acid and the reaction product 2-nitrophenylacetone: [7] Metal free meerwein arylation

  8. Category:Isopropenyl compounds - Wikipedia

    en.wikipedia.org/wiki/Category:Isopropenyl_compounds

    Isopropenyl esters (1 P) Pages in category "Isopropenyl compounds" The following 23 pages are in this category, out of 23 total. This list may not reflect recent ...

  9. Ketene - Wikipedia

    en.wikipedia.org/wiki/Ketene

    This is the Staudinger synthesis, a facile route to this important class of compounds. With acetone, ketene reacts to give isopropenyl acetate. [1] A variety of hydroxylic compounds can add as nucleophiles, forming either enol or ester products.