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  2. Diphenylphosphoryl azide - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphoryl_azide

    It is now suggested that this reaction proceeds through the intermediate mixed anhydride, resulting from attack by the nucleophilic carboxylate anion on the phosphorus atom, with expulsion of the azide ion. The latter then attacks the carbonyl carbon atom, to give the acyl azide and loss of the diphenylphosphate anion, known to be a good ...

  3. Curtius rearrangement - Wikipedia

    en.wikipedia.org/wiki/Curtius_rearrangement

    The acyl azide is usually made from the reaction of acid chlorides or anhydrides [6] with sodium azide [7] or trimethylsilyl azide. [8] Acyl azides are also obtained from treating acylhydrazines with nitrous acid. [9] Alternatively, the acyl azide can be formed by the direct reaction of a carboxylic acid with diphenylphosphoryl azide (DPPA ...

  4. Organic azide - Wikipedia

    en.wikipedia.org/wiki/Organic_azide

    The azide functional group can be shown by two resonance structures. An organic azide is an organic compound that contains an azide (– N 3) functional group. [1] Because of the hazards associated with their use, few azides are used commercially although they exhibit interesting reactivity for researchers.

  5. Phenyl azide - Wikipedia

    en.wikipedia.org/wiki/Phenyl_azide

    Phenyl azide is an organic compound with the formula C 6 H 5 N 3. It is one of the prototypical organic azides. It is a pale yellow oily liquid with a pungent odor. The structure consists of a linear azide substituent bound to a phenyl group. The C−N=N angle is approximately 116°.

  6. 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 ]

  7. Diphenylphosphite - Wikipedia

    en.wikipedia.org/wiki/Diphenylphosphite

    Diphenyl phosphite is a diorganophosphite with the formula (C 6 H 5 O) 2 P(O)H. The molecule is tetrahedral. It is a colorless viscous liquid. The compounds can be prepared by treating phosphorus trichloride with phenol. Many analogues can be prepared similarly.

  8. Pyrophosphate - Wikipedia

    en.wikipedia.org/wiki/Pyrophosphate

    In chemistry, pyrophosphates are phosphorus oxyanions that contain two phosphorus atoms in a P−O−P linkage. A number of pyrophosphate salts exist, such as disodium pyrophosphate (Na 2 H 2 P 2 O 7) and tetrasodium pyrophosphate (Na 4 P 2 O 7), among others.

  9. Pyrophosphoric acid - Wikipedia

    en.wikipedia.org/wiki/Pyrophosphoric_acid

    Pyrophosphoric acid, also known as diphosphoric acid, is the inorganic compound with the formula H 4 P 2 O 7 or, more descriptively, [(HO) 2 P(O)] 2 O. Colorless and odorless, it is soluble in water, diethyl ether, and ethyl alcohol.