2-METHYL-2-OXAZOLINE

  • CAS:1120-64-5
  • MF:C4H7NO
  • Purity:99%
  • Molecular Weight:85.1057
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Product Details

  • CAS: 1120-64-5
  • MF: C4H7NO
  • Appearance: clear colourless to very faint yellow liquid
  • Factory Sells Best Quality 2-METHYL-2-OXAZOLINE 1120-64-5 with steady supply

    • Molecular Formula:C4H7NO
    • Molecular Weight:85.1057
    • Appearance/Colour:clear colourless to very faint yellow liquid 
    • Vapor Pressure:28.4mmHg at 25°C 
    • Refractive Index:n20/D 1.434(lit.)  
    • Boiling Point:110 °C at 760 mmHg 
    • PKA:5.77±0.50(Predicted) 
    • Flash Point:20 °C 
    • PSA:21.59000 
    • Density:1.08 g/cm3 
    • LogP:-0.12940 

    2-METHYL-2-OXAZOLINE(Cas 1120-64-5) Usage

    Definition

    ChEBI: A 5-membered heterocyclic compound, which is substituted in the 2-position with a methyl group and which is often used as a monomer in polymerisation reactions.

    General Description

    2-Methyl-2-oxazoline undergoes polymerization with 2-butyl-2-oxazoline to form poly(2-oxazoline) block copolymer. It undergoes cationic ring-opening polymerization with 2-(dec-9-enyl)-2-oxazoline to yield copoly(2-oxazoline)s.

    InChI:InChI=1/C4H7NO/c1-4-5-2-3-6-4/h2-3H2,1H3

    1120-64-5 Relevant articles

    Synthesis of Δ2-1,3-oxazolines and Δ2-1,3-oxazines using potassium fluoride on alumina

    Mitchell,Benicewicz

    , p. 675 - 677 (1994)

    Potassium fluoride (40%) on alumina was ...

    Ultrasound-Accelerated, Concise, and Highly Efficient Synthesis of 2-Oxazoline Derivatives Using Heterogenous Calcium Ferrite Nanoparticles and Their DFT Studies

    Atri, Shalu,Bendi, Anjaneyulu,Rao, G. B. Dharma,Raza, Mohd Jamshaiya,Sharma, Nutan

    , (2021/11/12)

    A rapid and operationally simple approac...

    A mild and efficient synthesis of 2-oxazolines via transamidation- cyclodehydrosulfurisation of thioamides with 2-aminoethanol

    Goud, D. Raghavender,Pathak, Uma

    supporting information, p. 3678 - 3682 (2013/02/22)

    Transamidation of thioamides with 2-amin...

    Synthesis of 2-oxazolines via boron esters of N-(2-hydroxyethyl) amides

    Ilkgul, Baris,Gunes, Deniz,Sirkecioglu, Okan,Bicak, Niyazi

    experimental part, p. 5313 - 5315 (2010/11/03)

    A new, convenient, one-pot process is pr...

    Generation of cyclic ketene-N,X-acetals (X = O, S) from 2-alkyl-1,3-oxazolines and 2-alkyl-1,3-thiazolines. Reactions with acid chlorides, 1,3-diacid chlorides and N-(chlorocarbonyl) isocyanate

    Zhou, Aihua,Pittman Jr., Charles U.

    , p. 37 - 48 (2007/10/03)

    2-Alkyl-1,3-oxazolines, 2-alkyl-1,3-thia...

    1120-64-5 Process route

    ethanolamine
    141-43-5

    ethanolamine

    thioacetamide
    62-55-5

    thioacetamide

    2-methyl-4,5-dihydro-1,3-oxazole
    1120-64-5,26375-28-0

    2-methyl-4,5-dihydro-1,3-oxazole

    Conditions
    Conditions Yield
    With calcium ferrite; In water; at 50 ℃; for 0.416667h; Sonication; Green chemistry;
    50%
    <i>N</i>-(2-chloro-ethyl)-acetamide
    7355-58-0

    N-(2-chloro-ethyl)-acetamide

    2-methyl-4,5-dihydro-1,3-oxazole
    1120-64-5,26375-28-0

    2-methyl-4,5-dihydro-1,3-oxazole

    Conditions
    Conditions Yield
    With sodium hydride; In various solvent(s); below 50 deg C;
    75%
    With sulfolane; potassium fluoride on basic alumina; for 2h;
    75%
    With silver tetrafluoroborate; In acetonitrile; for 16h; Ambient temperature;
    With sodium methylate; In methanol; for 1h; Heating;

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    Antioxidant BHT 264

    CAS:128-37-0

    Purity:99%

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