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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

    Methyldichlorophosphine is produced by alkylation of phosphorus trichloride with methyl iodide followed by reduction of the resulting phosphonium salt with iron powder: [2] [3]

  4. 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.

  5. C01-A042 - Wikipedia

    en.wikipedia.org/wiki/C01-A042

    This article about an ester is a stub. You can help Wikipedia by expanding it.

  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.

  7. Phosphonate - Wikipedia

    en.wikipedia.org/wiki/Phosphonate

    General ester of phosphonic acid; in fact, the phosphorus has a formal charge of +1, the oxygen above it has a formal charge of −1, and the bond between them is single. In organic chemistry , phosphonates or phosphonic acids are organophosphorus compounds containing C−PO(OR) 2 groups , where R is an organic group ( alkyl , aryl ).

  8. Dichlorophenylphosphine - Wikipedia

    en.wikipedia.org/wiki/Dichlorophenylphosphine

    [1] [2] However, aluminum chloride often induces diarylation; a cleaner catalyst for monoarylation is stannic chloride. [2] The compound is an intermediate for the synthesis of other chemicals for instance dimethylphenylphosphine: C 6 H 5 PCl 2 + 2 CH 3 MgI → C 6 H 5 P(CH 3) 2 + 2 MgICl. Many tertiary phosphines can be prepared by this route. [3]

  9. A-242 - Wikipedia

    en.wikipedia.org/wiki/A-242

    A-242 has been added to Schedule 1 of the Annex on Chemicals of the Chemical Weapons Convention as of June 2020, and it has been explicitly named as an example compound for schedule 1.A.15. [ 2 ] [ 3 ] For chemicals listed in Schedule 1, the most stringent declaration and verification measures are in place combined with far-reaching limits and ...

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