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  2. Trimethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphite

    Trimethyl phosphite is an organophosphorus compound with the formula P(OCH 3) 3, often abbreviated P(OMe) 3.It is a colorless liquid with a highly pungent odor. It is the simplest phosphite ester and finds used as a ligand in organometallic chemistry and as a reagent in organic synthesis.

  3. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    Phosphite esters are typically prepared by treating phosphorus trichloride with an alcohol. For alkyl alcohols the displaced chloride ion can attack the phosphite, causing dealkylation to give a dialkylphosphite and an organochlorine compound. [1] [2] The overall reaction is as follows: PCl 3 + 3 C 2 H 5 OH → (C 2 H 5 O) 2 P(O)H + 2 HCl + C 2 ...

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

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

    Chemicals which can be used as weapons, or used in their manufacture, but which have no, or almost no, legitimate applications as well are listed in Schedule 1, whilst Schedule 2 is used for chemicals which have legitimate small-scale applications. The use of Schedule 1, 2, or 3 chemicals as weapons is banned by the Convention.

  5. Trimethyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphate

    Trimethyl phosphate is the trimethyl ester of phosphoric acid. It is a colourless, nonvolatile liquid. It is a colourless, nonvolatile liquid. It has some specialized uses in the production of other compounds.

  6. Dimethyl methylphosphonate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_methylphosphonate

    Dimethyl methylphosphonate can be prepared from trimethyl phosphite and a halomethane (e.g. iodomethane) via the Michaelis–Arbuzov reaction. [2]Dimethyl methylphosphonate is a schedule 2 chemical as it may be used in the production of chemical weapons.

  7. Category:Foul-smelling chemicals - Wikipedia

    en.wikipedia.org/wiki/Category:Foul-smelling...

    Trimethyl phosphite; Trimethylamine; Trimethylarsine; Trimethylphosphine; Trimethyltin chloride; V. Valeric acid; Z. Zinc phosphide This page was last edited on 26 ...

  8. Michaelis–Arbuzov reaction - Wikipedia

    en.wikipedia.org/wiki/Michaelis–Arbuzov_reaction

    The Michaelis–Arbuzov reaction is initiated with the S N 2 attack of the nucleophilic phosphorus species (1 - A phosphite) with the electrophilic alkyl halide (2) to give a phosphonium salt as an intermediate (3). These intermediates are occasionally stable enough to be isolated, such as for triaryl phosphites which do not react to form the ...

  9. Alkyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Alkyl_phosphate

    Alkyl phosphates belong to a group of organic compounds called organophosphates.They are esters of phosphoric acid H 3 PO 4 and corresponding alcohol.For example, the formula of methyl phosphate is CH 3-H 2 PO 4, dimethyl phosphate – (CH 3) 2 HPO 4 and trimethyl phosphate – (CH 3) 3 PO 4.