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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. Category:Pinacolyl esters - Wikipedia

    en.wikipedia.org/wiki/Category:Pinacolyl_esters

    Esters of pinacolyl alcohol. Pages in category "Pinacolyl esters" The following 3 pages are in this category, out of 3 total.

  5. 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.

  6. File:Alcohol general.svg - Wikipedia

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

    SVG version of en:Image:Alcohol_general.jpg, which was uploaded by en:User:Walkerma. Made in inkscape by tracing over the JPEG. Made in inkscape by tracing over the JPEG. Text was removed as per en:Wikipedia:Preparing images for upload .

  7. 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.

  8. Pharmacology of ethanol - Wikipedia

    en.wikipedia.org/wiki/Pharmacology_of_ethanol

    Alcohol is also converted into phosphatidylethanol (PEth, an unnatural lipid metabolite) by phospholipase D2. This metabolite competes with PIP 2 agonist sites on lipid-gated ion channels. [28] [29] The result of these direct effects is a wave of further indirect effects involving a variety of other neurotransmitter and neuropeptide systems. [25]

  9. Talk:Pinacolyl alcohol - Wikipedia

    en.wikipedia.org/wiki/Talk:Pinacolyl_alcohol

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