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16165-66-5

  • Product Name:hexylphosphonic acid diethyl ester
  • Molecular Formula:C10H23 O3 P
  • Purity:99%
  • Molecular Weight:222.265
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Product Details

  • CasNo: 16165-66-5
  • Molecular Formula: C10H23 O3 P
  • Buy High Grade hexylphosphonic acid diethyl ester, Offer 16165-66-5 with Best Price

    • Molecular Formula:C10H23 O3 P
    • Molecular Weight:222.265
    • Vapor Pressure:0.00569mmHg at 25°C 
    • Refractive Index:1.4820 (estimate) 
    • Boiling Point:282.6°Cat760mmHg 
    • Flash Point:138.6°C 
    • PSA:45.34000 
    • Density:0.964g/cm3 
    • LogP:3.83280 

    hexylphosphonic acid diethyl ester(Cas 16165-66-5) Usage

    Uses

    Diethyl Hexylphosphonate is an intermediate in the synthesis of Hexylphosphonic Dichloride (H295465). Hexylphosphonic Dichloride acts as a reagent for the preparation of enantiomeric phosphonates which are inhibitors of cholesterol esterase.

    InChI:InChI=1/C10H23O3P/c1-4-7-8-9-10-14(11,12-5-2)13-6-3/h4-10H2,1-3H3

    16165-66-5 Relevant articles

    Phosphonate inhibitors of antigen 85C, a crucial enzyme involved in the biosynthesis of the Mycobacterium tuberculosis cell wall

    Gobec, Stanislav,Plantan, Ivan,Mravljak, Janez,Wilson, Rosalind A.,Besra, Gurdyal S.,Kikelj, Danijel

    , p. 3559 - 3562 (2004)

    The first phosphonate inhibitors of anti...

    Synthesis and polymerization kinetics of acrylamide phosphonic acids and esters as new dentine adhesives

    Besse,Le Pluart,Cook,Pham,Madec

    , p. 149 - 157 (2013)

    In restorative dentistry, acrylamide mon...

    Conjugate Addition of Alkyl- and Vinyl-copper Complexes to α,β-Unsaturated Phosphonic Esters. Stereospecific Syntheses of γ,δ-Unsaturated Phosphonates

    Nicotra, Francesco,Panza, Luigi,Russo, Giovanni

    , p. 5 - 6 (1984)

    Alkylcopper complexes add to diethyl eth...

    Rotational Motions in n-Hexane Phosphonic Acid Diethyl Ester Studied Combining 2H, 13C, and 31P NMR. Analysis of the Phosphorus-31 Spin-Lattice Relaxation

    Petr, A.,Grossmann, G.,Klose, G.,Ahlnaes, T.,Goetze, T.

    , p. 231 - 242 (1986)

    Spin-lattice relaxation of 13C and 31P i...

    Direct conversion of phosphonates to phosphine oxides: An improved synthetic route to phosphines including the first synthesis of methyl JohnPhos

    Kendall, Alexander J.,Salazar, Chase A.,Martino, Patrick F.,Tyler, David R.

    supporting information, p. 6171 - 6178 (2015/02/19)

    The synthesis of tertiary phosphine oxid...

    16165-66-5 Process route

    1-Iodohexane
    638-45-9

    1-Iodohexane

    triethyl phosphite
    122-52-1

    triethyl phosphite

    diethyl hexylphosphonate
    16165-66-5

    diethyl hexylphosphonate

    Conditions
    Conditions Yield
    at 150 ℃; for 8h;
    85%
    at 150 ℃; for 8h;
    85%
     
     
    n-hexylphosphonic acid
    4721-24-8

    n-hexylphosphonic acid

    Triethyl orthoacetate
    78-39-7

    Triethyl orthoacetate

    diethyl hexylphosphonate
    16165-66-5

    diethyl hexylphosphonate

    Conditions
    Conditions Yield
    at 90 ℃; for 24h; Green chemistry;
    91%

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    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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