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  2. 3-Hydroxyacetophenone - Wikipedia

    en.wikipedia.org/wiki/3-hydroxyacetophenone

    Melting point: 96 °C (205 °F; 369 K) Boiling point: 296 °C (565 °F; 569 K) ... 3-Hydroxyacetophenone is a chemical compound. It is a component of castoreum, ...

  3. Hydroxyacetophenone - Wikipedia

    en.wikipedia.org/wiki/Hydroxyacetophenone

    4-Hydroxyacetophenone (p-hydroxyacetophenone, piceol) Index of chemical compounds with the same name This set index article lists chemical compounds articles associated with the same name.

  4. Acetophenone - Wikipedia

    en.wikipedia.org/wiki/Acetophenone

    Acetophenone is formed as a byproduct of the cumene process, the industrial route for the synthesis of phenol and acetone.In the Hock rearrangement of isopropylbenzene hydroperoxide, migration of a methyl group rather than the phenyl group gives acetophenone and methanol as a result of an alternate rearrangement of the intermediate:

  5. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    4-Hydroxyacetophenone monooxygenase is an enzyme that transforms piceol into O-acetylhydroquinone. This enzyme is found in Pseudomonas fluorescens. See also ...

  6. Arene substitution pattern - Wikipedia

    en.wikipedia.org/wiki/Arene_substitution_pattern

    Fractional crystallisation can be used to obtain pure para product, relying on the principle that it is less soluble than the ortho and thus will crystallise first. Care must be taken to avoid cocrystallisation of the ortho isomer. [2] Many nitro compounds' ortho and para isomers have quite different boiling points. These isomers can often be ...

  7. Hydroxyacetone - Wikipedia

    en.wikipedia.org/wiki/Hydroxyacetone

    Melting point: −17 °C (1 °F; 256 K) Boiling point: 145–146 °C (293–295 °F; 418–419 K) Vapor pressure: 7.5 hPa at 20 °C [2] Refractive index (n D)

  8. Does Salt Expire? Technically No, But You Should Ideally Use ...

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  9. Salicylaldehyde - Wikipedia

    en.wikipedia.org/wiki/Salicylaldehyde

    Salicylaldehyde is produced by condensation of phenol with formaldehyde to give hydroxybenzyl alcohol, which is oxidized to the aldehyde. [4] Salicylaldehydes in general are prepared by ortho-selective formylation reactions from the corresponding phenol, for instance by the Duff reaction, Reimer–Tiemann reaction, or by treatment with paraformaldehyde in the presence of magnesium chloride and ...