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  2. Phenethyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Phenethyl_alcohol

    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. It is slightly soluble in water (2 ml per 100 ml of H 2 O), but miscible with most organic solvents.

  3. Phenylethanolamine - Wikipedia

    en.wikipedia.org/wiki/Phenylethanolamine

    An early synthesis of phenylethanolamine was by the reduction of 2-nitro-1-phenyl-ethanol. [6] Other early syntheses are summarized in a paper by Hartung and Munch. [7] A more recent synthesis, providing a better yield, is by the reduction of benzoyl cyanide using LiAlH 4. [8]

  4. 2-Methoxyethanol - Wikipedia

    en.wikipedia.org/wiki/2-Methoxyethanol

    2-Methoxyethanol, or methyl cellosolve, is an organic compound with formula C 3 H 8 O 2 that is used mainly as a solvent.It is a clear, colorless liquid with an ether-like odor.

  5. 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:

  6. 1-Phenylethanol - Wikipedia

    en.wikipedia.org/wiki/1-phenylethanol

    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.

  7. Phenol ether - Wikipedia

    en.wikipedia.org/wiki/Phenol_ether

    However, this synthesis risks the self-condensation of alcohol itself (e.g. ethanol self-condenses to form diethyl ether). A more common and higher-yielding reaction is the Williamson ether synthesis , where a phenol is converted by a strong base to the phenoxide ion, which can subsequently be reacted with an alkyl halide via nucleophilic ...

  8. 2-Ethylphenol - Wikipedia

    en.wikipedia.org/wiki/2-Ethylphenol

    2-Ethylphenol is an organic compound with the formula C 2 H 5 C 6 H 4 OH. It is one of three isomeric ethylphenols. A colorless liquid, it occurs as an impurity in xylenols and as such is used in the production of commercial phenolic resins. It is produced by ethylation of phenol using ethylene or ethanol in the presence of aluminium phenolate. [2]

  9. Isobutanol - Wikipedia

    en.wikipedia.org/wiki/Isobutanol

    Isobutanol (IUPAC nomenclature: 2-methylpropan-1-ol) is an organic compound with the formula (CH 3) 2 CHCH 2 OH (sometimes represented as i-BuOH). This colorless, flammable liquid with a characteristic smell is mainly used as a solvent either directly or as its esters.