Photosensitive Materials & UV Curing Coatings
  • 5-Methyl-3-vinyl-2-oxazolidinone

    • Product Name   :   

      5-Methyl-3-vinyl-2-oxazolidinone

    • CAS No   :   

      3395-98-0

    • Project State   :   

      Commercial

    General Description

    Cost-effective and customizable 5-Methyl-3-vinyl-2-oxazolidinone 3395-98-0 for sale

    • Molecular Formula:C6H9NO2
    • Molecular Weight:127.143
    • Vapor Pressure:2.2-25Pa at 20-50℃ 
    • Boiling Point:78-81 °C(Press: 1.3 Torr) 
    • PKA:-0.39±0.40(Predicted) 
    • PSA:29.54000 
    • Density:1.085 g/cm3 
    • LogP:0.90850 

    3395-98-0 Relevant articles

    SYNTHESIS OF N-VINYL COMPOUNDS BY REACTING CYLIC NH-COMPOUNDS WITH ACETYLENE IN PRESENCE OF HOMOGENOUS CATALYST

    -

    Page/Page column 17; 21-22, (2021/06/26)

    Process to produce N-vinyl compounds by ...

    Phosphine-Catalyzed Vinylation at Low Acetylene Pressure

    Sitte, Nikolai A.,Menche, Maximilian,Tu?ina, Pavel,Bienewald, Frank,Sch?fer, Ansgar,Comba, Peter,Rominger, Frank,Hashmi, A. Stephen K.,Schaub, Thomas

    , p. 13041 - 13055 (2021/09/18)

    The vinylation of various nucleophiles w...

    Ruthenium-catalyzed synthesis of vinylamides at low acetylene pressure

    Semina, Elena,Tuzina, Pavel,Bienewald, Frank,Hashmi,Schaub, Thomas

    supporting information, p. 5977 - 5980 (2020/06/04)

    The reaction of cyclic amides with acety...

    Process for production of N-vinyl compound

    -

    , (2008/06/13)

    The present invention provides a process...

    3395-98-0 Process route

    5-methyl-1,3-oxazolidin-2-one
    1072-70-4

    5-methyl-1,3-oxazolidin-2-one

    acetylene
    74-86-2,25067-58-7

    acetylene

    5-methyl-3-vinyloxazolidin-2-one
    3395-98-0

    5-methyl-3-vinyloxazolidin-2-one

    Conditions
    Conditions Yield
    With [bis(2-methylallyl)cycloocta-1,5-diene]ruthenium(II); tributylphosphine; In toluene; at 100 ℃; for 16h; Reagent/catalyst; Autoclave; Glovebox;
    84%
    With tributylphosphine; In toluene; at 100 ℃; for 16h; Reagent/catalyst; Autoclave; Inert atmosphere; Glovebox;
    84%
    With tributylphosphine; In N,N-dimethyl acetamide; at 140 ℃; for 16h; under 1.5 Torr; Glovebox; Sealed tube; Autoclave;
    52%
    dimethylenecyclourethane
    497-25-6

    dimethylenecyclourethane

    acetylene
    74-86-2,25067-58-7

    acetylene

    5-methyl-3-vinyloxazolidin-2-one
    3395-98-0

    5-methyl-3-vinyloxazolidin-2-one

    Conditions
    Conditions Yield
    With tributylphosphine; In toluene; at 100 ℃; for 16h; Reagent/catalyst; Autoclave; Inert atmosphere; Glovebox;
    29%

    3395-98-0 Upstream products

    • 123403-99-6
      123403-99-6

      N-(1-methoxyethyl)-5-methyl-2-oxazolidone

    • 123404-00-2
      123404-00-2

      N-(1-propoxyethyl)-5-methyl-2-oxazolidone

    • 1072-70-4
      1072-70-4

      5-methyl-1,3-oxazolidin-2-one

    • 74-86-2
      74-86-2

      acetylene

    3395-98-0 Downstream products

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      N-<1-Benzamino-aethyl>-5-methyl-2-oxo-oxazolidin

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