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  2. Pinacolyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Pinacolyl_alcohol

    Pinacolyl alcohol (also known as 3,3-dimethylbutan-2-ol and as pine alcohol) is one of the isomeric hexanols and a secondary alcohol. Pinacolyl alcohol appears on the List of Schedule 2 substances of the Chemical Weapons Convention as a precursor for the nerve agent soman .

  3. File:Pinacolylalcohol.svg - Wikipedia

    en.wikipedia.org/wiki/File:Pinacolylalcohol.svg

    The following other wikis use this file: Usage on eu.wikipedia.org Pinakolil alkohol; Usage on fa.wikipedia.org پیناکولیل الکل; Usage on hu.wikipedia.org

  4. Pinacolone - Wikipedia

    en.wikipedia.org/wiki/Pinacolone

    Pinacolone (3,3-dimethyl-2-butanone) is an important ketone in organic chemistry.It is a colorless liquid with a slight peppermint or camphor odor. It is a precursor to triazolylpinacolone in the synthesis of the fungicide triadimefon and in synthesis of the herbicide metribuzin.

  5. Soman - Wikipedia

    en.wikipedia.org/wiki/Soman

    Soman (or GD, EA 1210, Zoman, PFMP, A-255, systematic name: O-pinacolyl methylphosphonofluoridate) [1] is an extremely toxic chemical substance. It is a nerve agent, interfering with normal functioning of the mammalian nervous system by inhibiting the enzyme cholinesterase.

  6. Policosanol - Wikipedia

    en.wikipedia.org/wiki/Policosanol

    A meta-analysis in 2005 concluded that human policosanol consumption is safe and well tolerated and is effective at lowering the blood cholesterol. [3] As of 2010, they were marketed as lipid-lowering agents in the Caribbean, Central and South America, and Canada. [1]

  7. 1-Pentanol - Wikipedia

    en.wikipedia.org/wiki/1-Pentanol

    1-Pentanol, (or n-pentanol, pentan-1-ol), is an organic compound with the formula CH 3 CH 2 CH 2 CH 2 CH 2 OH and is classified as a primary alcohol. [2] It is a colourless liquid with a distinctive aroma. It is one of 8 isomeric alcohols with the formula C 5 H 11 OH. It is used as a solvent, a biological drying agent and in the synthesis of ...

  8. Friedel–Crafts reaction - Wikipedia

    en.wikipedia.org/wiki/Friedel–Crafts_reaction

    1,3-Diisopropylbenzene is produced via transalkylation, a special form of Friedel–Crafts alkylation. It also allows alkyl chains to be added reversibly as protecting groups. This approach is used industrially in the synthesis of 4,4'-biphenol via the oxidative coupling and subsequent dealkylation of 2,6-di-tert-butylphenol. [11] [12]

  9. 1-Propanol - Wikipedia

    en.wikipedia.org/wiki/1-Propanol

    1-Propanol (also propan-1-ol, propanol, n-propyl alcohol) is a primary alcohol with the formula CH 3 CH 2 CH 2 OH and sometimes represented as PrOH or n-PrOH.It is a colourless liquid and an isomer of 2-propanol. 1-Propanol is used as a solvent in the pharmaceutical industry, mainly for resins and cellulose esters, and, sometimes, as a disinfecting agent.

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