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  2. Phosphorus trichloride - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride

    Phosphorus trichloride is an inorganic compound with the chemical formula PCl 3. A colorless liquid when pure, it is an important industrial chemical , being used for the manufacture of phosphites and other organophosphorus compounds .

  3. Phosphorus trichloride (data page) - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_trichloride...

    2 Structure and properties. 3 Thermodynamic properties. 4 Spectral data. 5 References. ... This page provides supplementary chemical data on phosphorus trichloride.

  4. Phosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride

    Phosphoryl chloride (commonly called phosphorus oxychloride) is a colourless liquid with the formula P O Cl 3. It hydrolyses in moist air releasing phosphoric acid and fumes of hydrogen chloride. It is manufactured industrially on a large scale from phosphorus trichloride and oxygen or phosphorus pentoxide. [4] It is mainly used to make ...

  5. Thiophosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Thiophosphoryl_chloride

    Thiophosphoryl chloride is an inorganic compound with the chemical formula P S Cl 3. [5] It is a colorless pungent smelling liquid that fumes in air. It is synthesized from phosphorus chloride and used to thiophosphorylate organic compounds, such as to produce insecticides.

  6. Organophosphorus chemistry - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_chemistry

    Phosphites, sometimes called phosphite esters, have the general structure P(OR) 3 with oxidation state +3. Such species arise from the alcoholysis of phosphorus trichloride: PCl 3 + 3 ROH → P(OR) 3 + 3 HCl. The reaction is general, thus a vast number of such species are known.

  7. Phosphorus halide - Wikipedia

    en.wikipedia.org/wiki/Phosphorus_halide

    Phosphorus trichloride is a major industrial chemical and widely used starting material for phosphorus chemistry. Phosphorus tribromide is used in organic chemistry to convert alcohols to alkyl bromides and carboxylic acids to acyl bromides ( e.g. in the Hell-Volhard-Zelinsky reaction ).

  8. 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 ...

  9. Phosphorochloridite - Wikipedia

    en.wikipedia.org/wiki/Phosphorochloridite

    In chemistry, phosphorochloridites are a class of organophosphorus compound with the formula (RO) 2 PCl (R = organic substituent). They are pyramidal in shape, akin to regular phosphites (P(OR) 3 ). They are usually colorless and sensitive toward hydrolysis and, to some extent, oxidation to the corresponding phosphorochloridates ((RO) 2 P(O)Cl).