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Chemical structure of piceol. Names Preferred IUPAC name. 1-(4-Hydroxyphenyl)ethan-1-one ... 4-Hydroxyacetophenone monooxygenase is an enzyme that transforms piceol ...
4-Hydroxyacetophenone (p-hydroxyacetophenone, piceol) This page was last edited on 27 February 2021, at 08:40 (UTC). Text is available under the Creative Commons ...
The 4 substrates of this enzyme are (4-hydroxyphenyl)ethan-1-one, NADPH, H +, and O 2, whereas its 3 products are hydroquinone acetate ester, NADP +, and H 2 O. This enzyme belongs to the family of oxidoreductases , specifically those acting on paired donors, with O2 as oxidant and incorporation or reduction of oxygen.
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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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-Toluic acid; o-Toluic acid; m-Toluic acid
It is an α-hydroxyketone, also called a ketol, and is the simplest hydroxy ketone structure. It is a colorless, distillable liquid. ... [4] Hydroxyacetone is ...
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 ]