enow.com Web Search

Search results

  1. Results from the WOW.Com Content Network
  2. Étard reaction - Wikipedia

    en.wikipedia.org/wiki/Étard_reaction

    For example, n-propylbenzene is oxidized to propiophenone, benzyl methyl ketone, and several chlorinated products, with benzyl methyl ketone being the major product. [ 7 ] [ 8 ] Another example arises from the Étard reaction of trans- decalin which results in a mixture of trans-9-decalol, spiro [4.5]decan-6-one, trans-1-decalone, cis-1 ...

  3. Ephedrine - Wikipedia

    en.wikipedia.org/wiki/Ephedrine

    Ephedrine works by inducing the release of norepinephrine and hence indirectly activating the α-and β-adrenergic receptors. [11] Chemically, ephedrine is a substituted amphetamine and is the (1R,2S)-enantiomer of β-hydroxy-N-methylamphetamine. [14] Ephedrine was first isolated in 1885 and came into commercial use in 1926.

  4. Phenylacetylcarbinol - Wikipedia

    en.wikipedia.org/wiki/Phenylacetylcarbinol

    L-pac produced by biotransformation of benzaldehyde Phenylacetylcarbinol ( PAC ) is an organic compound that has two enantiomers , one with R- and one with S-configuration. (R)-PAC, which is commonly called l -PAC , is known as a precursor in the synthesis of pharmaceuticals such as ephedrine and pseudoephedrine .

  5. Substituted amphetamine - Wikipedia

    en.wikipedia.org/wiki/Substituted_amphetamine

    This synthesis was a by-product of a search for ephedrine, a bronchodilator used to treat asthma extracted exclusively from natural sources. Over-the-counter use of substituted amphetamines was initiated in the early 1930s by the pharmaceutical company Smith, Kline & French (now part of GlaxoSmithKline ), as a medicine ( Benzedrine ) for colds ...

  6. History and culture of substituted amphetamines - Wikipedia

    en.wikipedia.org/wiki/History_and_culture_of...

    Diagnostic impurities are the naphthalenes 1-benzyl-methylnaphthalene and 1,3-dimethyl-2-phenylnaphthalene, [108] arising in the Nagai and Leuckart routes, and cis-or trans-1,2-dimethyl-3-phenylaziridine, ephedrine, or erythro-3,4-dimethyl- 5-phenyloxazolidine, arising in the Nagai and Emde routes; these are absent in the reductive amination ...

  7. Benzaldehyde - Wikipedia

    en.wikipedia.org/wiki/Benzaldehyde

    Amygdalin 2 H 2 O HCN benzaldehyde 2 × glucose 2 × Benzaldehyde contributes to the scent of oyster mushrooms (Pleurotus ostreatus). Reactions Benzaldehyde is easily oxidized to benzoic acid in air at room temperature, causing a common impurity in laboratory samples. Since the boiling point of benzoic acid is much higher than that of benzaldehyde, it may be purified by distillation. Benzyl ...

  8. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    Benzyl cyanide: phenylacetic acid, phenylacetone, amphetamine: Ephedrine, its salts, optical isomers, and salts of optical isomers methamphetamine: Ergonovine and its salts lysergic acid diethylamide: Ergotamine and its salts lysergic acid diethylamide: N-Acetylanthranilic acid, its esters, and its salts methaqualone

  9. 4-Fluoroephedrine - Wikipedia

    en.wikipedia.org/wiki/4-Fluoroephedrine

    [6] [1] It is the 4-fluoro analogue of ephedrine. [6] [1] The synthesis of 4-fluoroephedrine has been described. [7] It can serve as a precursor in the synthesis of 4-fluoromethamphetamine (4-FMA). [3] The predicted log P of 4-fluoroephedrine is 1.0. [6] For comparison, the predicted log P of ephedrine is 0.9. [8]