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  2. Phosphite ester - Wikipedia

    en.wikipedia.org/wiki/Phosphite_ester

    Phosphite esters may be used as reducing agents in more specialised cases. For example, triethylphosphite is known to reduce certain hydroperoxides to alcohols formed by autoxidation [7] (scheme). In this process the phosphite is converted to a phosphate ester. This reaction type is also utilized in the Wender Taxol total synthesis.

  3. Organophosphate - Wikipedia

    en.wikipedia.org/wiki/Organophosphate

    These are primarily the esters of phosphoric acid and can be mono‑esters, di‑esters or tri‑esters depending on the number of attached organic groups (abbreviated as 'R' in the image below). In general man‑made organophosphates are most often triesters, while biological organophosphates are usually mono- or di-esters.

  4. Safety data sheet - Wikipedia

    en.wikipedia.org/wiki/Safety_data_sheet

    An example SDS, including guidance for handling a hazardous substance and information on its composition and properties. A safety data sheet (SDS), [1] material safety data sheet (MSDS), or product safety data sheet (PSDS) is a document that lists information relating to occupational safety and health for the use of various substances and products.

  5. Phosphoric acids and phosphates - Wikipedia

    en.wikipedia.org/.../Phosphoric_acids_and_phosphates

    The general formula of a phosphoric acid is H n+2−2x P n O 3n+1−x, where n is the number of phosphorus atoms and x is the number of fundamental cycles in the molecule's structure, between 0 and ⁠ n + 2 / 2 ⁠. Pyrophosphate anion. Trimethyl orthophosphate.

  6. Category:Phosphate esters - Wikipedia

    en.wikipedia.org/wiki/Category:Phosphate_esters

    Download as PDF; Printable version; In other projects ... Pages in category "Phosphate esters" The following 76 pages are in this category, out of 76 total. ...

  7. Purple acid phosphatases - Wikipedia

    en.wikipedia.org/wiki/Purple_acid_phosphatases

    Purple acid phosphatases (PAPs) (EC 3.1.3.2) are metalloenzymes that hydrolyse phosphate esters and anhydrides under acidic condition. [1] [2] In their oxidised form, PAPs in solution are purple in colour. This is due to the presence of a dinuclear iron centre, [3] to which a tyrosine residue is connected via a charge transfer. [4]

  8. Phosphoryl chloride - Wikipedia

    en.wikipedia.org/wiki/Phosphoryl_chloride

    Like phosphate, POCl 3 is tetrahedral in shape. [6] It features three P−Cl bonds and one strong P–O bond, with an estimated bond dissociation energy of 533.5 kJ/mol. Unlike in the case of POF 3 , the Schomaker-Stevenson rule predicts appropriate bond length for the P–O bond only if the P–O bond is treated as a double bond, P=O.

  9. Organophosphorus chemistry - Wikipedia

    en.wikipedia.org/wiki/Organophosphorus_chemistry

    Phosphate esters have the general structure P(=O)(OR) 3 feature P(V). Such species are of technological importance as flame retardant agents, and plasticizers. Lacking a P−C bond, these compounds are in the technical sense not organophosphorus compounds but esters of phosphoric acid. Many derivatives are found in nature, such as ...