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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.
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.
1-Phenylethanol is the organic compound with the formula C 6 H 5 CH(OH)CH 3. It is one of the most commonly available chiral alcohols. It is a colorless liquid with a mild gardenia-hyacinth scent. [4] Phenylethanol is an aromatic alcohol, it has the role of mouse metabolite.
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 ...
2,3-Dimethyl-1-butanol; 3,3-Dimethyl-1-butanol This page was last edited on 27 March 2024, at 19:55 (UTC). Text is available under the Creative Commons Attribution ...
The enzyme phenylpyruvate decarboxylase (EC 4.1.1.43) catalyzes the chemical reaction phenylpyruvate ⇌ {\displaystyle \rightleftharpoons } phenylacetaldehyde + CO 2 This enzyme belongs to the family of lyases , specifically the carboxy-lyases, which cleave carbon-carbon bonds.
4 HCrO 4 − + 3 RCH 2 OH + 16 H + + 11 H 2 O → 4 [Cr(H 2 O) 6] 3+ + 3 RCOOH. The inorganic products are green, characteristic of chromium(III) aquo complexes. [2] Like many other oxidations of alcohols by metal oxides, the reaction proceeds via the formation of a mixed chromate ester: [3] [4] These esters have the formula CrO 3 (OCH 2 R) −
The pharmacokinetics of phenylethanolamine, after intravenous administration to dogs, were studied by Shannon and co-workers, who found that the drug followed the "two-compartment model", with T 1/2 (α) ≃ 6.8 mins and T 1/2 (β) ≃ 34.2 mins; the "plasma half-life" of phenylethanolamine was therefore about 30 minutes. [15]