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  2. Acetanilide - Wikipedia

    en.wikipedia.org/wiki/Acetanilide

    Acetanilide can be produced by reacting acetic anhydride with aniline: [7]. C 6 H 5 NH 2 + (CH 3 CO) 2 O → C 6 H 5 NHCOCH 3 + CH 3 COOH. The preparation used to be a traditional experiment in introductory organic chemistry lab classes, [8] but it has now been widely replaced by the preparation of either paracetamol or aspirin, both of which teach the same practical techniques (especially ...

  3. Acetamide - Wikipedia

    en.wikipedia.org/wiki/Acetamide

    Acetamide (systematic name: ethanamide) is an organic compound with the formula CH 3 CONH 2. It is an amide derived from ammonia and acetic acid. It finds some use as a plasticizer and as an industrial solvent. [5] The related compound N,N-dimethylacetamide (DMA) is more widely used, but it is not prepared from acetamide.

  4. Phenylethanolamine - Wikipedia

    en.wikipedia.org/wiki/Phenylethanolamine

    The pharmacokinetics of phenylethanolamine, after intravenous administration to dogs, were studied by Shannon and co-workers, who found that the drug followed the "two-compartment model", with T 1/2 (α) ≃ 6.8 mins and T 1/2 (β) ≃ 34.2 mins; the "plasma half-life" of phenylethanolamine was therefore about 30 minutes. [15]

  5. Phenethylamine - Wikipedia

    en.wikipedia.org/wiki/Phenethylamine

    Substituted phenethylamines are a chemical class of organic compounds based upon the phenethylamine structure; [note 2] the class is composed of all the derivative compounds of phenethylamine which can be formed by replacing, or substituting, one or more hydrogen atoms in the phenethylamine core structure with substituents.

  6. Ethylamine - Wikipedia

    en.wikipedia.org/wiki/Ethylamine

    Ethylamine, also known as ethanamine, is an organic compound with the formula CH 3 CH 2 NH 2. This colourless gas has a strong ammonia-like odor. It condenses just below room temperature to a liquid miscible with virtually all solvents. It is a nucleophilic base, as is typical for amines.

  7. Category:Phenethylamines - Wikipedia

    en.wikipedia.org/wiki/Category:Phenethylamines

    Phenethylamine (1-amino-2-phenyl ethane) is a monoamine compound. Substitutions to the phenethylamine molecule give rise to a group of compounds collectively known as substituted phenethylamines or phenethylamines.

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  9. Substituted phenethylamine - Wikipedia

    en.wikipedia.org/wiki/Substituted_phenethylamine

    Substituted phenethylamines (or simply phenethylamines) are a chemical class of organic compounds that are based upon the phenethylamine structure; [note 1] the class is composed of all the derivative compounds of phenethylamine which can be formed by replacing, or substituting, one or more hydrogen atoms in the phenethylamine core structure with substituents.