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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 .
Pinacol is a branched alcohol which finds use in organic syntheses. It is a diol that has hydroxyl groups on vicinal carbon atoms. A white solid that melts just above room temperature, pinacol is notable for undergoing the pinacol rearrangement in the presence of acid and for being the namesake of the pinacol coupling reaction.
The α-methyl group can participate in condensation reactions. The carbonyl group can undergo the usual reactions (hydrogenation, reductive amination, etc.). It is a Schedule 3 compound under the Chemical Weapons Convention 1993, due to being related to pinacolyl alcohol, which is used in the production of soman. [2]
This list is ordered by the number of carbon atoms in an alcohol. C1. Methanol; C2. Ethanol; C3. 1-Propanol; Isopropyl alcohol; C4 n-Butanol; Isobutanol; sec-Butanol ...
Pinacolyl alcohol This page was last edited on 27 April 2015, at 13:11 (UTC). Text is available under the Creative Commons Attribution-ShareAlike 4 ...
Pinacolyl alcohol; Q. QL (chemical) QL sulfide; T. 3,3,5-Trimethylcyclohexanol This page was last edited on 11 June 2018, at 13:55 (UTC). Text is available under the ...
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
Esters of pinacolyl alcohol. Pages in category "Pinacolyl esters" The following 3 pages are in this category, out of 3 total.