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814-22-2

  • Product Name：diethyl propyl phosphate
  • Molecular Formula：C7H17 O4 P
  • Purity：99%
  • Molecular Weight：196.183
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Product Details

  • CasNo： 814-22-2
  • Molecular Formula： C7H17 O4 P

    • Offer Factory Supply diethyl propyl phosphate 814-22-2 Fast Shipping

    • Molecular Formula:C7H17 O4 P
    • Molecular Weight:196.183
    • Vapor Pressure:0.099mmHg at 25°C 
    • Boiling Point:230.6°C at 760 mmHg 
    • Flash Point:107.4°C 
    • PSA：54.57000 
    • Density:1.047g/cm3 
    • LogP:2.59410 

    1-diethoxyphosphoryloxypropane(Cas 814-22-2) Usage

    InChI:InChI=1/C7H17O4P/c1-4-7-11-12(8,9-5-2)10-6-3/h4-7H2,1-3H3

    814-22-2 Relevant articles

    The Atherton-Todd reactions under sonochemical activation

    Oussaid,Soufiaoui,Garrigues

    , p. 871 - 875 (1995)

    Alcohols 1a-g phosphorylation is perform...

    Kinetics and adsorption calculations: insights into the MgO-catalyzed detoxification of simulants of organophosphorus biocides

    Almerindo, Gizelle I.,Buratto, Suelen C.,Caramori, Giovanni F.,Fiedler, Haidi D.,Medeiros, Michelle,Micke, Gustavo A.,Nicolazi, Lucas M.,Nome, Faruk,Parreira, Renato L. T.,Sangaletti, Patrícia,Schneider, Felipe S. S.,Wanderlind, Eduardo H.

    , p. 19011 - 19021 (2020/10/02)

    We report the targeted decomposition of ...

    LiI/TBHP Mediated Oxidative Cross-Coupling of P(O)–H Compounds with Phenols and Various Nucleophiles: Direct Access to the Synthesis of Organophosphates

    Anitha, Thippani,Ashalu, Kashamalla Chinna,Sandeep, Mummadi,Mohd, Aabid,Wencel-Delord, Joanna,Colobert, Francoise,Reddy, Kallu Rajender

    , p. 7463 - 7474 (2019/12/03)

    An efficient and mild method for the dir...

    Method for synthesis of organophosphorus compound by photo-induced iodine catalyzed Atherton-Todd reaction

    -

    Paragraph 0031, (2018/12/14)

    The invention belongs to the technical f...

    Erratum: Cross-hetero-dehydrogenative coupling reaction of phosphites: A catalytic metal-free phosphorylation of amines and alcohols (Organic Letters (2013) 15:23 (6062) DOI: 10.1021/ol402956b)

    Dhineshkumar, Jayaraman,Prabhu, Kandikere Ramaiah

    supporting information, p. 326 - 326 (2014/01/23)

    -

    814-22-2 Process route

    propan-1-ol
    71-23-8

    propan-1-ol

    O,O-diethyl S-methyl phosphorothioate
    2404-05-9

    O,O-diethyl S-methyl phosphorothioate

    methanesulfonic acid
    75-75-2,98527-29-8

    methanesulfonic acid

    diethyl n-propyl phosphate
    814-22-2

    diethyl n-propyl phosphate

    Conditions
    Conditions Yield
    With 3-chloro-benzenecarboperoxoic acid;
    		 
    propan-1-ol
    71-23-8

    propan-1-ol

    phosphonic acid diethyl ester
    762-04-9

    phosphonic acid diethyl ester

    diethyl n-propyl phosphate
    814-22-2

    diethyl n-propyl phosphate

    Conditions
    Conditions Yield
    With water; dihydrogen peroxide; iodine; In neat (no solvent); at 20 ℃;
    		95%
    With dihydrogen peroxide; iodine; In water; at 20 ℃;
    		95%
    With triethylamine; In tetrachloromethane; for 2.5h; ultrasonic irradiation;
    		86%
    With iodine; oxygen; In dichloromethane; at 20 ℃; for 24h; Irradiation;
    		82%
    With sodium hydroxide; tetrabutylammomium bromide; In tetrachloromethane; dichloromethane; at 15 ℃; for 3h;
    		70.5%
    With sodium hydroxide; tetrabutylammomium bromide; In tetrachloromethane;
    		 
    With tert.-butylhydroperoxide; lithium iodide; In water; acetonitrile; at 20 ℃; for 0.25h;
    		147mg

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    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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