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  2. Phenylpropanoic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylpropanoic_acid

    Phenylpropanoic acid or hydrocinnamic acid is a carboxylic acid with the formula C 9 H 10 O 2 belonging to the class of phenylpropanoids. It is a white, crystalline solid with a sweet, floral scent at room temperature. Phenylpropanoic acid has a wide variety of uses including cosmetics, food additives, and pharmaceuticals. [5]

  3. Phenylalanine (data page) - Wikipedia

    en.wikipedia.org/wiki/Phenylalanine_(data_page)

    Download as PDF; Printable version; ... alpha-Amino-beta-phenylpropionic acid (2R)-2-amino-3- phenylpropanoic acid (2S)-2-amino-3-phenylpropanoic acid ... Reliability ...

  4. Phenylpropiolic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylpropiolic_acid

    Chromic acid oxidizes it to benzoic acid; zinc and acetic acid reduce it to cinnamic acid, C 6 H 5 CH=CHCO 2 H, whilst sodium amalgam reduces it to hydrocinnamic acid, C 6 H 5 CH 2 CH 2 CO 2 H. Ortho-nitrophenylpropiolic acid, NO 2 C 6 H 4 CCCO 2 H, prepared by the action of alcoholic potash on ortho-nitrocinnamic acid dibromide, crystallizes ...

  5. Reduction of nitro compounds - Wikipedia

    en.wikipedia.org/wiki/Reduction_of_nitro_compounds

    Raney nickel, platinum on carbon, or zinc dust and formic acid or ammonium formate [6] α,β-Unsaturated nitro compounds can be reduced to saturated amines by: Catalytic hydrogenation over palladium-on-carbon; Iron metal; Lithium aluminium hydride [27] (Note: Hydroxylamines and oximes are typical impurities.)

  6. Phenyl alkanoic acids - Wikipedia

    en.wikipedia.org/wiki/Phenyl_alkanoic_acids

    Phenylacetic, 3-phenylpropanoic and 3-phenylpropenoic acids are found in propolis, mammalian exocrine secretions or plant fragrances. During a systematic study of the lipids from seeds of the plant Araceae, [1] the presence of 13-phenyltridecanoic acid as a major component (5-16% of total fatty acids)was discovered. Other similar compounds but ...

  7. Chemical stability - Wikipedia

    en.wikipedia.org/wiki/Chemical_stability

    In chemistry, chemical stability is the thermodynamic stability of a chemical system, in particular a chemical compound or a polymer. [1] Colloquially, it may instead refer to kinetic persistence , the shelf-life of a metastable substance or system; that is, the timescale over which it begins to degrade.

  8. File:Phenylpropanoic acid.svg - Wikipedia

    en.wikipedia.org/wiki/File:Phenylpropanoic_acid.svg

    The following other wikis use this file: Usage on de.wikipedia.org 3-Phenylpropansäure; Usage on eo.wikipedia.org Natria fenil-propanato; Fenilpropionata acido

  9. Pourbaix diagram - Wikipedia

    en.wikipedia.org/wiki/Pourbaix_diagram

    Pourbaix diagram of iron. [1] The Y axis corresponds to voltage potential. In electrochemistry, and more generally in solution chemistry, a Pourbaix diagram, also known as a potential/pH diagram, E H –pH diagram or a pE/pH diagram, is a plot of possible thermodynamically stable phases (i.e., at chemical equilibrium) of an aqueous electrochemical system.