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  2. Thionyl chloride - Wikipedia

    en.wikipedia.org/wiki/Thionyl_chloride

    Thionyl chloride is an inorganic compound with the chemical formula SOCl 2.It is a moderately volatile, colourless liquid with an unpleasant acrid odour.Thionyl chloride is primarily used as a chlorinating reagent, with approximately 45,000 tonnes (50,000 short tons) per year being produced during the early 1990s, [5] but is occasionally also used as a solvent.

  3. von Braun amide degradation - Wikipedia

    en.wikipedia.org/wiki/Von_Braun_amide_degradation

    The von Braun amide degradation is the chemical reaction of a monosubstituted amide with phosphorus pentachloride or thionyl chloride to give a nitrile and an organohalide. [1] It is named after Julius Jacob von Braun, who first reported the reaction. [2] [3] The von Braun amide degradation

  4. Phosphorus trichloride - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride

    Phosphorus trichloride is an inorganic compound with the chemical formula PCl 3. A colorless liquid when pure, it is an important industrial chemical , being used for the manufacture of phosphites and other organophosphorus compounds .

  5. Methylphosphonyl dichloride - Wikipedia

    en.wikipedia.org/wiki/Methylphosphonyl_dichloride

    Methylphosphonyl dichloride is produced by oxidation of methyldichlorophosphine, with sulfuryl chloride: [3] CH 3 PCl 2 + SO 2 Cl 2 → CH 3 P(O)Cl 2 + SOCl 2. It can also be produced from a range of methylphosphonates (e.g. dimethyl methylphosphonate) via chlorination with thionyl chloride. Various amines catalyse this process. [4]

  6. List of Schedule 3 substances (CWC) - Wikipedia

    en.wikipedia.org/wiki/List_of_Schedule_3...

    Schedule 3 substances, in the sense of the Chemical Weapons Convention, are chemicals which have large-scale industrial uses, but are feasible to use as toxic chemical weapons (Part A) or manufacturing precursors (Part B).

  7. Beckmann rearrangement - Wikipedia

    en.wikipedia.org/wiki/Beckmann_rearrangement

    The Beckmann rearrangement is often catalyzed by acid; however, other reagents have been known to promote the rearrangement. These include tosyl chloride, thionyl chloride, phosphorus pentachloride, phosphorus pentoxide, triethylamine, sodium hydroxide, trimethylsilyl iodide among others. [3]

  8. People exposed to white phosphorus can suffer severe and sometimes deadly bone-deep burns. It can cause organs to shut down, and burns on just 10% of the body can be fatal, HRW said.

  9. Organochlorine chemistry - Wikipedia

    en.wikipedia.org/wiki/Organochlorine_chemistry

    Alkyl chlorides are most easily prepared by treating alcohols with thionyl chloride (SOCl 2) or phosphorus pentachloride (PCl 5), but also commonly with sulfuryl chloride (SO 2 Cl 2) and phosphorus trichloride (PCl 3): ROH + SOCl 2 → RCl + SO 2 + HCl 3 ROH + PCl 3 → 3 RCl + H 3 PO 3 ROH + PCl 5 → RCl + POCl 3 + HCl