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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. Melting points of the elements (data page) - Wikipedia

    en.wikipedia.org/wiki/Melting_points_of_the...

    The Gmelin rare earths handbook lists 1522 °C and 1550 °C as two melting points given in the literature, the most recent reference [Handbook on the chemistry and physics of rare earths, vol.12 (1989)] is given with 1529 °C.

  6. o-Xylene - Wikipedia

    en.wikipedia.org/wiki/O-Xylene

    o-Xylene (ortho-xylene) is an aromatic hydrocarbon with the formula C 6 H 4 (CH 3) 2, with two methyl substituents bonded to adjacent carbon atoms of a benzene ring (the ortho configuration). It is a constitutional isomer of m-xylene and p-xylene, the mixture being called xylene or xylenes. o-Xylene is a colourless slightly oily flammable ...

  7. 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 ...

  8. Hydroxyacetone - Wikipedia

    en.wikipedia.org/wiki/Hydroxyacetone

    It undergoes rapid polymerization, including forming a hemiacetal cyclic dimer.Under alkaline conditions, it undergoes a rapid aldol condensation.. Hydroxyacetone can be produced by degradation of various sugars.

  9. Triethyl orthoformate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_orthoformate

    Triethyl orthoformate is an organic compound with the formula HC(OC 2 H 5) 3.This colorless volatile liquid, the ortho ester of formic acid, is commercially available.The industrial synthesis is from hydrogen cyanide and ethanol.