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  2. Phosphonate - Wikipedia

    en.wikipedia.org/wiki/Phosphonate

    Phosphonic esters are prepared using the Michaelis–Arbuzov reaction. For example, methyl iodide catalyses the conversion of trimethylphosphite to the phosphonate ester dimethyl methylphosphonate: P(OMe) 3 → MePO(OMe) 2. These esters can be hydrolysed to the acid (Me = methyl): MePO(OMe) 2 + H 2 O → MePO(OH) 2 + 2 MeOH

  3. Organophosphate - Wikipedia

    en.wikipedia.org/wiki/Organophosphate

    Organophosphate flame retardants are part of a wider family of phosphorus-based agents which include organic phosphonate and phosphinate esters, in addition to inorganic salts. [ 56 ] [ 57 ] When some prominent brominated flame retardant were banned in the early 2000s phosphorus-based agents were promoted as safer replacements.

  4. Category:Phosphonate esters - Wikipedia

    en.wikipedia.org/wiki/Category:Phosphonate_esters

    Pages in category "Phosphonate esters" The following 18 pages are in this category, out of 18 total. This list may not reflect recent changes. A. Armine (chemical) B.

  5. Category:Phosphonates - Wikipedia

    en.wikipedia.org/wiki/Category:Phosphonates

    Phosphonates are salts (M 2 HPO 3) or esters (OP(OR) 2 R) of phosphonic acid Wikimedia Commons has media related to Phosphonates . The main article for this category is Phosphonate .

  6. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    The general structure of a phosphite ester showing the lone pairs on the P. In organic chemistry, a phosphite ester or organophosphite usually refers to an organophosphorous compound with the formula P(OR) 3. They can be considered as esters of an unobserved tautomer phosphorous acid, H 3 PO 3, with the simplest example being trimethylphosphite ...

  7. Triethyl phosphite - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphite

    Triethyl phosphite (TEP) is an organophosphorus compound, specifically a phosphite ester, with the formula P(OCH 2 CH 3) 3, often abbreviated P(OEt) 3. It is a colorless, malodorous liquid. It is used as a ligand in organometallic chemistry and as a reagent in organic synthesis.

  8. Triethyl phosphonoacetate - Wikipedia

    en.wikipedia.org/wiki/Triethyl_phosphonoacetate

    Triethyl phosphonoacetate is a reagent for organic synthesis used in the Horner-Wadsworth-Emmons reaction (HWE) or the Horner-Emmons modification.. Triethyl phosphonoacetate can be added dropwise to sodium methoxide solution to prepare a phosphonate anion.

  9. Dimethylphosphite - Wikipedia

    en.wikipedia.org/wiki/Dimethylphosphite

    Dimethylphosphite is an organophosphorus compound with the formula (CH 3 O) 2 P(O)H, known as dimethyl hydrogen phosphite (DMHP). Dimethylphosphite, is a minor tautomer of the phosphorus(V) derivative.