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  2. Trimethyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Trimethyl_phosphate

    Trimethyl phosphate is a mild methylating agent, useful for dimethylation of anilines and related heterocyclic compounds. [2] The method is complementary to the traditional Eschweiler-Clarke reaction in cases where formaldehyde engages in side reactions.

  3. 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.

  4. Ortho ester - Wikipedia

    en.wikipedia.org/wiki/Ortho_ester

    Examples of orthoesters include the reagents trimethyl orthoformate and triethylorthoacetate. Another example is the bicyclic OBO protecting group (4-methyl-2,6,7-trioxa-bicyclo[2.2.2]octan-1-yl) which is formed by the action of (3-methyloxetan-3-yl)methanol on activated carboxylic acids in the presence of Lewis acids. The group is base stable ...

  5. Tris(trimethylsilyl)phosphine - Wikipedia

    en.wikipedia.org/wiki/Tris(trimethylsilyl)phosphine

    Tris(trimethylsilyl)phosphine is the organophosphorus compound with the formula P(SiMe 3) 3 (Me = methyl). It is a colorless liquid that ignites in air and hydrolyses readily. It is a colorless liquid that ignites in air and hydrolyses readily.

  6. Trimethylphosphine - Wikipedia

    en.wikipedia.org/wiki/Trimethylphosphine

    Trimethylphosphine is a highly basic ligand that forms complexes with most metals. As a ligand, trimethylphosphine's Tolman cone angle is 118°. [7] This angle is an indication of the amount of steric protection that this ligand provides to the metal that to which it is bound.

  7. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    Phosphites are oxidized to phosphate esters: P(OR) 3 + [O] → OP(OR) 3. This reaction underpins the commercial use of some phosphite esters as stabilizers in polymers. [6] Alkyl phosphite esters are used in the Perkow reaction for the formation of vinyl phosphonates, and in the Michaelis–Arbuzov reaction to form phosphonates.

  8. Alkyl phosphate - Wikipedia

    en.wikipedia.org/wiki/Alkyl_phosphate

    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. Alkyl phosphates are widely distributed in nature, and form the basis of most biological processes. For example, high energy metabolites such as ATP and PEP are alkyl phosphates, as are nucleic acids ...

  9. Thiophosphate - Wikipedia

    en.wikipedia.org/wiki/Thiophosphate

    Dithiophosphate has the formula [PO 2 S 2] 3−, which has C 2v symmetry. Sodium dithiophosphate, which is colorless, is the major product from the reaction of phosphorus pentasulfide with NaOH: [6] P 2 S 5 + 6 NaOH → 2 Na 3 PO 2 S 2 + H 2 S + 2 H 2 O. Dithiophosphoric acid is obtained by treatment of barium dithiophosphate with sulfuric acid:

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