1445-75-6

  • Product Name:Diisopropyl methylphosphonate
  • Molecular Formula:C7H17 O3 P
  • Purity:99%
  • Molecular Weight:180.184
Get the best price

Product Details

  • CasNo: 1445-75-6
  • Molecular Formula: C7H17 O3 P
  • Chinese Manufacturer Supply Top Purity 99% Diisopropyl methylphosphonate 1445-75-6 Competitive Price

    • Molecular Formula:C7H17 O3 P
    • Molecular Weight:180.184
    • Vapor Pressure:0.000475mmHg at 25°C 
    • Melting Point:25°C 
    • Refractive Index:1.4100 
    • Boiling Point:214.5°Cat760mmHg 
    • Flash Point:97.7°C 
    • PSA:45.34000 
    • Density:0.991g/cm3 
    • LogP:2.65930 

    DIISOPROPYL METHYLPHOSPHONATE(Cas 1445-75-6) Usage

    Uses

    Diisopropyl methylphosphonate is used as a precursor to prepare beta-keto phosphonates. It acts as an intermediate for Horner-Wadsworth-Emmons olefination of carbonyl compounds.

    Definition

    ChEBI: An organic phosphonate that is the diisopropyl ester of methylphosphonic acid.

    InChI:InChI=1/C7H17O3P/c1-5(2)7(6(3)4)11(8,9)10/h5-7H,1-4H3,(H2,8,9,10)/p-2

    1445-75-6 Relevant articles

    Structure and reactivity of mixed alkali metal alkoxide/aryloxide catalysts

    Kissling,Gagne

    , p. 9005 - 9010 (2001)

    The average solution aggregation state o...

    Solvent-Free Michaelis-Arbuzov Rearrangement under Flow Conditions

    Jasiak, Aleksandra,Mielniczak, Grazyna,Owsianik, Krzysztof,Koprowski, Marek,Krasowska, Dorota,Drabowicz, Józef

    , p. 2619 - 2625 (2019)

    The first solvent- and catalyst-free pro...

    Phase-transfer-catalyzed Michaelis-Becker synthesis of dialkyl methyl phosphonates

    Fakhraian, Hossein,Mirzaei, Akbar

    , p. 511 - 518 (2006)

    A liquid-liquid phase-transfer-catalyzed...

    Stereocontrolled synthesis of planar chiral carba-paracyclophanes via modular assembly

    Jung, Sunna,Kitajima, Yoko,Ueda, Yasuyuki,Suzuki, Keisuke,Ohmori, Ken

    , p. 1521 - 1526 (2016)

    Described herein is a flexible modular a...

    Microwave-assisted ionic liquid-catalyzed selective monoesterification of alkylphosphonic acids—an experimental and a theoretical study

    ábrányi-Balogh, Péter,Drahos, László,Harsági, Nikoletta,Henyecz, Réka,Keglevich, Gy?rgy

    , (2021/09/07)

    It is well-known that the P-acids includ...

    PHOSPHONATE CONJUGATES AND USES THEREOF

    -

    Paragraph 0089, (2020/07/31)

    Phosphonate conjugates, preferably, bisp...

    Discovery of phosphonamidate IDO1 inhibitors for the treatment of non-small cell lung cancer

    Du, Qianming,Feng, Xi,Wang, Yinuo,Xu, Xi,Zhang, Yan,Qu, Xinliang,Li, Zhiyu,Bian, Jinlei

    , (2019/08/26)

    Targeting indoleamine 2,3-dioxygenase 1 ...

    1445-75-6 Process route

    triisopropyl phosphite
    116-17-6

    triisopropyl phosphite

    1,1-dibromomethane
    74-95-3

    1,1-dibromomethane

    Tetraisopropyl methylenediphosphonate
    1660-95-3

    Tetraisopropyl methylenediphosphonate

    diisopropyl hydrogenphosphonate
    1809-20-7

    diisopropyl hydrogenphosphonate

    triisopropyl phosphate
    513-02-0

    triisopropyl phosphate

    diisopropyl methanephosphonate
    1445-75-6

    diisopropyl methanephosphonate

    diisopropyl isopropylphosphonate
    3759-39-5

    diisopropyl isopropylphosphonate

    diisopropyl (bromomethyl)phosphonate
    98432-80-5

    diisopropyl (bromomethyl)phosphonate

    Conditions
    Conditions Yield
    In ethylbenzene; xylene; at 125 ℃; for 24h; under 760.051 - 2052.96 Torr; Product distribution / selectivity;
    50%
    triisopropyl phosphite
    116-17-6

    triisopropyl phosphite

    1,1-dibromomethane
    74-95-3

    1,1-dibromomethane

    Tetraisopropyl methylenediphosphonate
    1660-95-3

    Tetraisopropyl methylenediphosphonate

    triisopropyl phosphate
    513-02-0

    triisopropyl phosphate

    diisopropyl methanephosphonate
    1445-75-6

    diisopropyl methanephosphonate

    diisopropyl isopropylphosphonate
    3759-39-5

    diisopropyl isopropylphosphonate

    diisopropyl phosphite
    691-96-3

    diisopropyl phosphite

    diisopropyl (bromomethyl)phosphonate
    98432-80-5

    diisopropyl (bromomethyl)phosphonate

    Conditions
    Conditions Yield
    In toluene; at 120 ℃; for 24h; under 760.051 - 2259.82 Torr;
    50%

    1445-75-6 Upstream products

    • 74-83-9
      74-83-9

      methyl bromide

    • 116-17-6
      116-17-6

      triisopropyl phosphite

    • 676-97-1
      676-97-1

      methylphosphonic acid dichloroanhydride

    • 67-63-0
      67-63-0

      isopropyl alcohol

    1445-75-6 Downstream products

    • 1445-76-7
      1445-76-7

      methylphosphonic chloride isopropyl ester

    • 676-97-1
      676-97-1

      methylphosphonic acid dichloroanhydride

    • 146286-13-7
      146286-13-7

      [2-Hydroxy-2-(4-isopropenyl-cyclohex-1-enyl)-ethyl]-phosphonic acid diisopropyl ester

    • 123381-19-1
      123381-19-1

      (2R,3S)-diisopropyl <3-(t-Boc-amino)-4-cyclohexyl-2-hydroxybutyl>phosphonate

    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

    Contact Now

    We will contact you as soon as possible


    提交