1072-53-3

  • Product Name:1,3,2-Dioxathiolane 2,2-dioxide
  • Molecular Formula:C2H4 O4 S
  • Purity:99%
  • Molecular Weight:124.117
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Product Details

  • CasNo: 1072-53-3
  • Molecular Formula: C2H4 O4 S
  • Appearance: yellowish crystal
  • Cost-effective and customizable 1,3,2-Dioxathiolane 2,2-dioxide 1072-53-3 factory

    • Molecular Formula:C2H4 O4 S
    • Molecular Weight:124.117
    • Appearance/Colour:yellowish crystal 
    • Vapor Pressure:0.0965mmHg at 25°C 
    • Melting Point:95-97 °C(lit.) 
    • Refractive Index:1.469 
    • Boiling Point:231.1 °C at 760 mmHg 
    • Flash Point:93.5 °C 
    • PSA:60.98000 
    • Density:1.604 g/cm3 
    • LogP:0.35880 

    ETHYLENESULFATE(Cas 1072-53-3) Usage

    InChI:InChI=1/C2H4O4S/c3-7(4)5-1-2-6-7/h1-2H2

    1072-53-3 Relevant articles

    -

    Kaiser et al.

    , p. 602 (1963)

    -

    Kinetic resolutions concentrate the minor enantiomer and aid measurement of high enantiomeric purity

    Caron,Tseng,Kazlauskas

    , p. 83 - 92 (1994)

    Although many methods can measure enanti...

    -

    Baker,Field

    , p. 86,87 (1932)

    -

    High yield synthesis of cyclic phosphites, phosphates, sulphites and sulphates of catechol and glycol mediated by hypervalent silicon centres

    Kingston,Sudheendra Rao

    , p. 4841 - 4844 (1997)

    Room temperature reactions of both tris(...

    -

    Lipkin,Layloff

    , p. 450,451 (1970)

    -

    Preparation method of ethylene sulfate derivative

    -

    Paragraph 0027-0028; 0029-0030; 0031-0032; 0035-0040, (2021/01/25)

    The invention belongs to the technical f...

    Synthesis method of ethylene sulfate

    -

    Paragraph 0031; 0033-0044, (2021/04/21)

    The invention discloses a synthesis meth...

    Synthesis process of ethylene sulfate

    -

    Paragraph 0019; 0021-0022; 0024-0025; 0027-0028; 0030-0031, (2021/02/20)

    The invention discloses a synthesis proc...

    Preparation method of cyclic sulfate

    -

    Paragraph 0014; 0019-0020, (2021/01/29)

    The invention discloses a preparation me...

    1072-53-3 Process route

    ethylene sulfite
    3741-38-6

    ethylene sulfite

    ethyleneglycol sulfate
    1072-53-3

    ethyleneglycol sulfate

    Conditions
    Conditions Yield
    With manganese(IV) oxide; In water; at 5 ℃; for 0.75h; Reagent/catalyst; Temperature;
    95.84%
    With sodium hydrogencarbonate; iron(II) sulfate; In dichloromethane; pH=7 - 8; Concentration;
    90.66%
    With ruthenium trichloride; calcium hypochlorite; at 15 ℃;
    83%
    With ruthenium(III) chloride trihydrate; trichloroisocyanuric acid; tetrabutylammomium bromide; potassium carbonate; In water; acetonitrile; at 20 - 60 ℃; for 2h; Temperature; Reagent/catalyst; Solvent;
    83.3%
    With ruthenium trichloride; calcium hypochlorite; In acetic acid butyl ester; water; at -15 - -10 ℃; for 10h; Solvent;
    83%
    With sodium hypochlorite; water; at 0 - 5 ℃; for 0.5h; Large scale;
    82.4%
    With dihydrogen peroxide; In dichloromethane; tert-butyl methyl ether; at 40 ℃; for 5h; Large scale;
    82.4%
    With sodium hypochlorite; ruthenium tetroxide; In tetrachloromethane; water; for 1.5h; Ambient temperature;
    73%
    With ruthenium tetroxide; In chloroform; water; at 0 ℃; for 0.0125h;
    72%
    With ruthenium trichloride; sodium hypochlorite; sodium hydrogencarbonate; In dichloromethane; water;
    70%
    With potassium sulfate; rhenium(III) chloride; Marshall's acid; potassium carbonate; In dichloromethane; water; at 0 - 4 ℃; for 1h;
    68.1%
    With sodium periodate; ruthenium(III) chloride trihydrate; In dichloromethane; water; at 0 - 5 ℃; for 2h; Inert atmosphere;
    60%
    With ruthenium trichloride; sodium periodate; In water; acetonitrile; at 0 ℃; for 0.0833333h;
    With ruthenium trichloride; sodium periodate; In water; acetonitrile; at 0 - 25 ℃; for 1h; Yield given;
    With ruthenium(III) chloride trihydrate; In tetrachloromethane; acetonitrile;
    With ruthenium(IV) oxide; In isopropyl alcohol; acetonitrile; at 40 - 45 ℃; for 6h; Temperature; Solvent; Reagent/catalyst;
    98 g
    With ruthenium trichloride; sodium hypochlorite; potassium dihydrogenphosphate; at 0 - 10 ℃; for 0.5h; Reagent/catalyst;
    172 g
    With tert.-butylhydroperoxide; copper(l) chloride; In water; at 35 ℃; for 2.75h; Temperature;
    115.5 g
    ethylene glycol
    107-21-1

    ethylene glycol

    ethyleneglycol sulfate
    1072-53-3

    ethyleneglycol sulfate

    Conditions
    Conditions Yield
    With fluorosulfonyl fluoride; N,N,N,N,-tetramethylethylenediamine; In acetonitrile; at 60 ℃; for 36h; Reagent/catalyst; Solvent; Temperature;
    96.5%
    ethylene glycol; With fluorosulfonyl fluoride; sodium sulfate; tetra(n-butyl)ammonium hydrogensulfate; sodium hydroxide; In tert-butyl methyl ether; at 5 - 10 ℃; for 1h; Autoclave;
    With 15-crown-5; 18-crown-6 ether; In dichloromethane; Solvent; Reagent/catalyst; Temperature;
    81.8%
    With potassium hydroxide; sulfuryl dichloride; silica gel; Yield given. Multistep reaction; 1.) reflux; 2.) rt., 3 h;
    ethylene glycol; With potassium hydroxide; In 5,5-dimethyl-1,3-cyclohexadiene; at 130 - 140 ℃; for 20h;
    With fluorosulfonyl fluoride; In acetonitrile; at -15 - -5 ℃; for 1h; Temperature; Reagent/catalyst; Solvent; Sealed tube; Inert atmosphere;
    106.3 g
    With sulfuryl dichloride; In chloroform; at 5 - 60 ℃; for 3h;
    375 g

    1072-53-3 Upstream products

    • 106-93-4
      106-93-4

      ethylene dibromide

    • 3741-38-6
      3741-38-6

      ethylene sulfite

    • 74-85-1
      74-85-1

      ethene

    • 107-21-1
      107-21-1

      ethylene glycol

    1072-53-3 Downstream products

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      sulfuric acid mono-(2-amino-ethyl ester)

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      2-(benzylamino)ethyl hydrogen sulfate

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