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  • ...[Image:Thionyl chloride.png|center|thumb|250px|{{#ifexist:Template:Thionyl chloride.png/credit|{{Cefaclor.jpg/credit}}<br/>|}}]] |molname=thionyl chloride
    1 KB (135 words) - 18:39, 28 November 2010
  • ...de]] is reacted with [[ethylene]] to first produce [[2-chloroethylsulfenyl chloride]] which is converted by a second addition of ethylene to mustard gas. ...roduction of mustard gas. While there are more applications for [[thionyl chloride]], both are in the least restrictive [[Chemical Weapons Convention/Schedul
    6 KB (977 words) - 01:06, 29 January 2011
  • *[[Aluminium chloride]] &ndash; AlCl<sub>3</sub> *[[Ammonium chloride]] &ndash; NH<sub>4</sub>Cl
    26 KB (3,687 words) - 04:49, 23 January 2011
  • | O-Isopropyl methylphosphonochloridate (1445-76-7) | O-Pinacolyl methylphosphonochloridate (7040-57-5)
    5 KB (597 words) - 13:35, 24 January 2011
  • ...to have exported [[thiodiglycol]] (a mustard gas precursor) and [[thionyl chloride]] (a nerve gas precursor) to Iraq in 1988 and 1989. <ref name=FT1991-07-29
    28 KB (4,221 words) - 12:32, 12 September 2013