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  2. Methylphosphonyl dichloride - Wikipedia

    en.wikipedia.org/wiki/Methylphosphonyl_dichloride

    Methylphosphonyl dichloride (DC) or dichloro is an organophosphorus compound. It has commercial application in oligonucleotide synthesis, [1] but is most notable as being a precursor to several chemical weapons agents. It is a white crystalline solid that melts slightly above room temperature. [2]

  3. Methyldichlorophosphine - Wikipedia

    en.wikipedia.org/wiki/Methyldichlorophosphine

    Methyl phosphonous dichloride, Dichloromethylphosphine, SW [1 ... The compound is an intermediate for the synthesis of other chemicals for instance ...

  4. Dimethyl methylphosphonate - Wikipedia

    en.wikipedia.org/wiki/Dimethyl_methylphosphonate

    It will react with thionyl chloride to produce methylphosphonic acid dichloride, which is used in the production of sarin and soman nerve agents. Various amines can be used to catalyse this process. [3] It can be used as a sarin-simulant for the calibration of organophosphorus detectors.

  5. Phosphonate - Wikipedia

    en.wikipedia.org/wiki/Phosphonate

    Toggle Synthesis subsection. 2.1 From phosphonic acid. ... 3 product can then be decomposed with water to produce an alkylphosphonic dichloride RP(=O)Cl 2. Reactions

  6. Methylphosphonic acid - Wikipedia

    en.wikipedia.org/wiki/Methylphosphonic_acid

    Methylphosphonic acid is an organophosphorus compound with the chemical formula CH 3 P(O)(OH) 2. The phosphorus center is tetrahedral and is bonded to a methyl group, two OH groups and an oxygen. Methylphosphonic acid is a white, non-volatile solid that is poorly soluble in organic solvent but soluble in water and common alcohols.

  7. Methylphosphonyl difluoride - Wikipedia

    en.wikipedia.org/wiki/Methylphosphonyl_difluoride

    Methylphosphonyl difluoride is both reactive and corrosive. It is absorbed through skin and causes burns and mild nerve agent symptoms. It reacts with water, producing HF fumes and methylphosphonic acid as a result. It is also capable of corroding glass.

  8. 3,3,5-Trimethylcyclohexyl 3-pyridyl methylphosphonate - Wikipedia

    en.wikipedia.org/wiki/3,3,5-Trimethylcyclohexyl...

    Methylphosphonic dichloride and triethylamine are dissolved in benzene. 3,3,5-Trimethylcyclohexanol is then slowly added while stirring and cooling. The reaction temperature is maintained at 10-15 °C. The mixture is then heated to 40 °C for 1 hour. A benzene solution of 3,3,5-trimethylcyclohexyl methylphosphonochloridate is formed.

  9. Methylphosphine - Wikipedia

    en.wikipedia.org/wiki/Methylphosphine

    The compound exhibits the properties characteristic of a primary phosphine, i.e., a compound of the type RPH 2.It can be oxidized to methylphosphonous acid: . MePH 2 + O 2 → MeP(H)O 2 H