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1-Phenylethanol is found in nature as a glycoside, together with its hydrolase β-primeverosidase in tea (Camellia sinensis) flowers. [7] It is also reportedly present in cranberries, grapes, chives, Scottish spearmint oil, cheeses, cognac, rum, white wine, cocoa, black tea, filbert, cloudberries, beans, mushrooms, and endives.
Phenethyl alcohol, or 2-phenylethanol, is an organic compound with the chemical formula C 6 H 5 CH 2 CH 2 OH.It is a colourless liquid with a pleasant floral odor. It occurs widely in nature, being found in a variety of essential oils.
Phenylethanol may refer to: 1-Phenylethanol; 2-Phenylethanol (phenethyl alcohol) This page was last edited on 22 October 2023, at 17:24 (UTC). Text is available ...
This hydroperoxide is then used to oxidize propylene to propylene oxide, which is also recovered as a co-product. The remaining 1-phenylethanol is dehydrated to give styrene: The remaining 1-phenylethanol is dehydrated to give styrene:
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:
Cetyl alcohol (1-hexadecanol) 16 carbon atoms: C 16 H 34 O Palmitoleyl alcohol (cis-9-hexadecen-1-ol) 16 carbon atoms: unsaturated: C 16 H 32 O Heptadecyl alcohol (1-n-heptadecanol, heptadecanol) 17 carbon atoms: C 17 H 36 O Stearyl alcohol (1-octadecanol) 18 carbon atoms: C 18 H 38 O Oleyl alcohol (1-octadecenol) 18 carbon atoms: unsaturated ...
Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers. [1] Phenylacetaldehyde is an aldehyde that consists of acetaldehyde bearing a phenyl substituent; the parent member of the phenylacetaldehyde class of compounds.
In this process, chain growth is optimized to produce alcohols with narrow molecular weight distribution. Synthesis of other alcohols use Ziegler and the updated EPAL process, such as the transalkylation of styrene to form 2-phenylethanol. Diethylaluminum hydride can be employed in place of triethylaluminium. [1]