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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. Phenylpropanoid - Wikipedia

    en.wikipedia.org/wiki/Phenylpropanoid

    The phenylpropanoids are a diverse family of organic compounds that are biosynthesized by plants from the amino acids phenylalanine and tyrosine in the shikimic acid pathway. [1] Their name is derived from the six-carbon, aromatic phenyl group and the three-carbon propene tail of coumaric acid , which is the central intermediate in ...

  4. 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 ...

  5. Phenylpropiolic acid - Wikipedia

    en.wikipedia.org/wiki/Phenylpropiolic_acid

    Phenylpropiolic acid, C 6 H 5 CCCO 2 H, formed by the action of alcoholic potash on cinnamic acid dibromide, C 6 H 5 CHBrCHBrCO 2 H, crystallizes in long needles or prisms which melt at 136–137 °C. When heated with water to 120 °C, it yields phenylacetylene (C 6 H 5 CCH).

  6. Hypothetical types of biochemistry - Wikipedia

    en.wikipedia.org/wiki/Hypothetical_types_of...

    Water as a solvent limits the forms biochemistry can take. For example, Steven Benner, proposes the polyelectrolyte theory of the gene that claims that for a genetic biopolymer such as, DNA, to function in water, it requires repeated ionic charges. [46] If water is not required for life, these limits on genetic biopolymers are removed.

  7. Dehydration reaction - Wikipedia

    en.wikipedia.org/wiki/Dehydration_reaction

    The classic example of a dehydration reaction is the Fischer esterification, which involves treating a carboxylic acid with an alcohol to give an ester RCO 2 H + R′OH ⇌ RCO 2 R′ + H 2 O Often such reactions require the presence of a dehydrating agent, i.e. a substance that reacts with water.

  8. Reductive amination - Wikipedia

    en.wikipedia.org/wiki/Reductive_amination

    In biochemistry, dehydrogenase enzymes use reductive amination to produce the amino acid glutamate. Additionally, there is ongoing research on alternative synthesis mechanisms with various metal catalysts which allow the reaction to be less energy taxing, and require milder reaction conditions.

  9. Hydrobiology - Wikipedia

    en.wikipedia.org/wiki/Hydrobiology

    An example of a mountain lake ecosystem. Hydrobiology is the science of life and life processes in water. Much of modern hydrobiology can be viewed as a sub-discipline of ecology but the sphere of hydrobiology includes taxonomy, economic and industrial biology, morphology, and physiology.