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  2. Butyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Butyraldehyde

    Butyraldehyde, also known as butanal, is an organic compound with the formula CH 3 (CH 2) 2 CHO. This compound is the aldehyde derivative of butane . It is a colorless flammable liquid with an unpleasant smell.

  3. γ-Hydroxybutyraldehyde - Wikipedia

    en.wikipedia.org/wiki/Γ-hydroxybutyraldehyde

    Like 1,4-BD, it also behaves as a prodrug to GHB when taken exogenously. However, as with all aliphatic aldehydes , γ-hydroxybutaldehyde is caustic and is strong-smelling and foul-tasting; thus, actual ingestion of this compound is likely to be unpleasant and result in severe nausea and vomiting .

  4. Sodium phenylbutyrate - Wikipedia

    en.wikipedia.org/wiki/Sodium_phenylbutyrate

    Sodium phenylbutyrate, sold under the brand name Buphenyl among others, is a salt of an aromatic fatty acid, 4-phenylbutyrate (4-PBA) or 4-phenylbutyric acid. [7] The compound is used to treat urea cycle disorders, because its metabolites offer an alternative pathway to the urea cycle to allow excretion of excess nitrogen.

  5. TPPTS - Wikipedia

    en.wikipedia.org/wiki/Tppts

    TPPTS was first synthesized in 1975 by E.G Kuntz who was an engineer at Rhône-Poulenc with the aim of carrying out a two-phase homogeneous catalysis in which the aqueous phase catalyst could be easily separated from the reaction products and recycled. [4] Using TPPTS, allowed him to prepare water-soluble complexes with Rh(I), Ni(0), Pd(0).

  6. Aldol condensation - Wikipedia

    en.wikipedia.org/wiki/Aldol_condensation

    An aldol condensation is a condensation reaction in organic chemistry in which two carbonyl moieties (of aldehydes or ketones) react to form a β-hydroxyaldehyde or β-hydroxyketone (an aldol reaction), and this is then followed by dehydration to give a conjugated enone.

  7. Aldol reaction - Wikipedia

    en.wikipedia.org/wiki/Aldol_reaction

    [2] [3] [4] The aldol reaction is paradigmatic in organic chemistry and one of the most common means of forming carbon–carbon bonds in organic chemistry. [5] [6] [7] It lends its name to the family of aldol reactions and similar techniques analyze a whole family of carbonyl α-substitution reactions, as well as the diketone condensations.

  8. 1-Butanol - Wikipedia

    en.wikipedia.org/wiki/1-Butanol

    1-Butanol, also known as butan-1-ol or n-butanol, is a primary alcohol with the chemical formula C 4 H 9 OH and a linear structure. Isomers of 1-butanol are isobutanol, butan-2-ol and tert-butanol. The unmodified term butanol usually refers to the straight chain isomer.

  9. 3-Hydroxybutanal - Wikipedia

    en.wikipedia.org/wiki/3-Hydroxybutanal

    In organic chemistry, 3-hydroxybutanal (acetaldol, aldol) is an organic compound with the formula CH 3 CH(OH)CH 2 CHO and the structure H 3 C−CH()−CH 2 −CH=O.It is classified as an aldol (R−CH(OH)−CHR'−C(=O)−R") and the word "aldol" can refer specifically to 3-hydroxybutanal.