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  2. Hydroxyacetophenone - Wikipedia

    en.wikipedia.org/wiki/Hydroxyacetophenone

    3-Hydroxyacetophenone (m-hydroxyacetophenone) 4-Hydroxyacetophenone (p-hydroxyacetophenone, piceol) This page was last edited on 27 February ...

  3. Chloromethyl group - Wikipedia

    en.wikipedia.org/wiki/Chloromethyl_group

    Structure of the chloromethyl group. In organic chemistry, the chloromethyl group is a functional group that has the chemical formula −CH 2 −Cl. The naming of this group is derived from the methyl group (which has the formula −CH 3), by replacing one hydrogen atom by a chlorine atom. Compounds with this group are a subclass of the ...

  4. Piceol - Wikipedia

    en.wikipedia.org/wiki/Piceol

    This page was last edited on 21 October 2024, at 18:13 (UTC).; Text is available under the Creative Commons Attribution-ShareAlike 4.0 License; additional terms may apply.

  5. 3-Hydroxyacetophenone - Wikipedia

    en.wikipedia.org/wiki/3-hydroxyacetophenone

    3-Hydroxyacetophenone is a chemical compound. It is a component of castoreum, the exudate from the castor sacs of the mature beaver. [1] Related compounds.

  6. C8H8O2 - Wikipedia

    en.wikipedia.org/wiki/C8H8O2

    The molecular formula C 8 H 8 O 2 may refer to: Anisaldehyde (p-anisaldehyde) Benzodioxan; 3,4-Dihydroxystyrene; 3-Hydroxyacetophenone; 2-Hydroxy-4-methylbenzaldehyde; 4-Hydroxyphenylacetaldehyde; 2-Methoxybenzaldehyde (o-anisaldehyde) Methyl benzoate; Phenyl acetate; Phenylacetic acid; Piceol and other hydroxy acetophenones; Toluic acids. p ...

  7. 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:

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  9. Chloroalkyl ether - Wikipedia

    en.wikipedia.org/wiki/Chloroalkyl_ether

    Chemical structure of chloromethyl methyl ether (MOM-Cl) Chloroalkyl ethers are a class of organic compounds with the general structure R-O-(CH 2) n-Cl, characterized as an ether connected to a chloromethyl group via an alkane chain. Chloromethyl methyl ether (CMME) is an ether with the formula C H 3 OCH 2 Cl.

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