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  2. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    Acetophenone is the organic compound with the formula C 6 H 5 C(O)CH 3. It is the simplest aromatic ketone . This colorless, viscous liquid is a precursor to useful resins and fragrances.

  3. File:Acetophenone-2D-skeletal.svg - Wikipedia

    en.wikipedia.org/wiki/File:Acetophenone-2D...

    Skeletal formula of the acetophenone molecule. Structure based on information reported in Acta Cryst. (1973). B29, 1822–1826. Image generated in ChemDraw Professional 20.0 and converted into SVG file using Scribus 1.5.4 + Inkscape 1.0.1 (drawn according to official Manual of Style guidelines) Date: 2 April 2021: Source: Own work: Author: Chem ...

  4. Ketone - Wikipedia

    en.wikipedia.org/wiki/Ketone

    In organic chemistry, a ketone / ˈ k iː t oʊ n / is an organic compound with the structure R−C(=O)−R', where R and R' can be a variety of carbon-containing substituents. Ketones contain a carbonyl group −C(=O)− (a carbon-oxygen double bond C=O). The simplest ketone is acetone (where R and R' is methyl), with the formula (CH 3) 2 CO ...

  5. Acetone - Wikipedia

    en.wikipedia.org/wiki/Acetone

    Acetone (2-propanone or dimethyl ketone) is an organic compound with the formula (CH 3) 2 CO. [22] It is the simplest and smallest ketone ( >C=O ). It is a colorless, highly volatile , and flammable liquid with a characteristic pungent odour, very reminiscent of the smell of pear drops .

  6. Cumene hydroperoxide - Wikipedia

    en.wikipedia.org/wiki/Cumene_hydroperoxide

    Cumene hydroperoxide is the organic compound with the formula C 6 H 5 C(CH 3) 2 OOH. An oily liquid, it is classified as an organic hydroperoxide. [2] Products of decomposition of cumene hydroperoxide are methylstyrene, acetophenone, and 2-phenyl-2-propanol. [3] It is produced by treatment of cumene with oxygen, an autoxidation.

  7. Pyrylium - Wikipedia

    en.wikipedia.org/wiki/Pyrylium

    Pyrylium salts are easily produced from simple starting materials through a condensation reaction. [2]Pyrylium salts with aromatic substituents, such 2,4,6-triphenylpyrylium tetrafluoroborate, can be obtained from two moles of acetophenone, one mole of benzaldehyde, and excess tetrafluoroboric acid. [3]

  8. Bisphenol - Wikipedia

    en.wikipedia.org/wiki/Bisphenol

    The bisphenols (/ ˈ b ɪ s f ɪ n ɒ l /) are a group of industrial chemical compounds related to diphenylmethane; commonly used in the creation of plastics and epoxy resins. [ 1 ] [ 2 ] [ 3 ] Most are based on two hydroxyphenyl functional groups linked by a methylene bridge .

  9. 2,4,6-Trihydroxyacetophenone - Wikipedia

    en.wikipedia.org/wiki/2,4,6-Trihydroxyacetophenone

    2,4,6-Trihydroxyacetophenone (THAP) is a chemical compound that is a derivative of phloroglucinol. In an animal model, THAP was reported to enhance cholesterol 7 alpha-hydroxylase (CYP7A1) activity. [ 1 ]