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  2. Phenyl-2-nitropropene - Wikipedia

    en.wikipedia.org/wiki/Phenyl-2-nitropropene

    In the lab, phenyl-2-nitropropene is produced by the reaction of benzaldehyde and nitroethane in the presence of a basic catalyst like n-butylamine.The reaction is a nitroaldol reaction, and is a variant of a Knoevenagel condensation reaction, which is one of a broader class of reactions called Henry condensations, or simply Henry reactions.

  3. Nitroethane - Wikipedia

    en.wikipedia.org/wiki/Nitroethane

    Via condensations like the Henry reaction, nitroethane converts to several compounds of commercial interest.Condensation with 3,4-dimethoxybenzaldehyde affords the precursor to the antihypertensive drug methyldopa; condensation with unsubstituted benzaldehyde yields phenyl-2-nitropropene, a precursor for amphetamine drugs.

  4. Phenylacetone - Wikipedia

    en.wikipedia.org/wiki/Phenylacetone

    Phenylacetone, also known as phenyl-2-propanone, is an organic compound with the chemical formula C 6 H 5 CH 2 COCH 3. It is a colorless oil that is soluble in organic solvents. It is a mono-substituted benzene derivative, consisting of an acetone attached to a phenyl group. As such, its systematic IUPAC name is 1-phenyl-2-propanone.

  5. C9H9NO2 - Wikipedia

    en.wikipedia.org/wiki/C9H9NO2

    2,6-Diacetylpyridine; Phenyl-2-nitropropene (P2NP) This page was last edited on 27 June 2021, at 17:58 (UTC). Text is available under the Creative Commons ...

  6. 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 ...

  7. Phenylpropene - Wikipedia

    en.wikipedia.org/wiki/Phenylpropene

    Phenylpropenes broadly are compounds containing a phenyl ring bonded to propene, more specifically those with an allyl group bonded to a benzene ring, having the parent structure of allylbenzene. These comprise a class of phenylpropanoids , where there are typically other substituents bonded to the aromatic ring.

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  9. DEA list of chemicals - Wikipedia

    en.wikipedia.org/wiki/DEA_list_of_chemicals

    Phenyl-2-nitropropene: substituted amphetamines: 1-(4-bromophenyl)propan-1-one substituted cathinones and substituted amphetamines: 1-(4-chlorophenyl)propan-1-one substituted cathinones and substituted amphetamines: 1-(4-methylphenyl)propan-1-one substituted cathinones and substituted amphetamines: Carbonyldiimidazole: LSD: 1,1-Dichloro-1 ...

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