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  2. 4-Fluoroephedrine - Wikipedia

    en.wikipedia.org/wiki/4-Fluoroephedrine

    4-Fluoroephedrine, also known as 4-fluoro-β-hydroxy-N-methylamphetamine, is a substituted phenethylamine, amphetamine, and β-hydroxyamphetamine derivative. [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 ...

  3. 4-Fluoroaniline - Wikipedia

    en.wikipedia.org/wiki/4-Fluoroaniline

    4-Fluoroaniline can be prepared by the hydrogenation of 4-nitrofluorobenzene. [2] It is a common building block in medicinal chemistry and related fields. [3] For example, it is a precursor to the fungicide fluoroimide or the fentanyl analogue parafluorofentanyl. It has also been evaluated for the production of ligands for homogeneous catalysis ...

  4. 4-Fluoronitrobenzene - Wikipedia

    en.wikipedia.org/wiki/4-Fluoronitrobenzene

    It is one of three isomeric fluoronitrobenzenes. [2] A yellow oil, it is prepared from 4-nitrochlorobenzene using the Halex process: O 2 NC 6 H 4 Cl + KF → O 2 NC 6 H 4 F + KCl. 4-Fluoronitrobenzene can be hydrogenated to give 4-fluoroaniline, [3] which is a precursor to the fungicide fluoroimide and parafluorofentanyl.

  5. Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/Nitroaniline

    The term nitroaniline in chemistry refers to a derivative of aniline (C 6 H 5 NH 2) containing a nitro group (—NO 2) There are three simple nitroanilines of formula C 6 H 4 (NH 2)(NO 2) which differ only in the position of the nitro group: 2-Nitroaniline; 3-Nitroaniline; 4-Nitroaniline

  6. Ephedrine - Wikipedia

    en.wikipedia.org/wiki/Ephedrine

    Ephedrine Sulphate (1932), Ephedrine Compound (1932), and Swan-Myers Ephedrine Inhalant No. 66 (circa 1940).Ephedrine is a non-catecholamine sympathomimetic with cardiovascular effects similar to those of adrenaline/epinephrine: increased blood pressure, heart rate, and contractility.

  7. 2-Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/2-Nitroaniline

    2-Nitroaniline is prepared commercially by the reaction of 2-nitrochlorobenzene with ammonia: [2] ClC 6 H 4 NO 2 + 2 NH 3 → H 2 NC 6 H 4 NO 2 + NH 4 Cl. Many other methods exist for the synthesis of this compound. Direct nitration of aniline is inefficient since anilinium is produced instead. Nitration of acetanilide gives only traces of 2 ...

  8. Low-Alcohol Beers Are Trending Like Never Before — Here Are ...

    www.aol.com/low-alcohol-beers-trending-never...

    Guinness Draught (4.2% ABV) Guinness, an Irish Dry Stout, is a fantastic example to disprove a common misconception, that dark beers are higher in alcohol. Malt has nothing to do with alcohol content.

  9. 4-Nitroaniline - Wikipedia

    en.wikipedia.org/wiki/4-Nitroaniline

    4-Nitroaniline, p-nitroaniline or 1-amino-4-nitrobenzene is an organic compound with the formula C 6 H 6 N 2 O 2. A yellow solid, it is one of three isomers of nitroaniline. It is an intermediate in the production of dyes, antioxidants, pharmaceuticals, gasoline, gum inhibitors, poultry medicines, and as a corrosion inhibitor. [3]