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2-Ethyl-2-oxazoline

Basic Information

  • CAS No.: 10431-98-8

Physical properties

Product Description

Factory Sells Best Quality 2-Ethyl-2-oxazoline 10431-98-8 with USP

  • Molecular Formula: C5H9NO
  • Molecular Weight: 99.1326
  • Appearance/Colour: clear liquid 
  • Vapor Pressure: 13mmHg at 25°C 
  • Melting Point: -62 °C(lit.) 
  • Refractive Index: n20/D 1.437(lit.)  
  • Boiling Point: 128.4 °C at 760 mmHg 
  • PKA: 5.65±0.50(Predicted) 
  • Flash Point: 29.4 °C 
  • PSA: 21.59000 
  • Density: 1.05 g/cm3 
  • LogP: 0.26070 

2-Ethyl-2-oxazoline(Cas 10431-98-8) Usage

Flammability and Explosibility

Notclassified

General Description

2-Ethyl-2-oxazoline undergoes cationic ring opening graft polymerization using tosylated cellulose nanowhisker as macroinitiator.

InChI:InChI=1/C5H9NO/c1-2-5-6-3-4-7-5/h2-4H2,1H3

10431-98-8 Relevant articles

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

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

, p. 5313 - 5315 (2010)

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

Sulfonimidation via ring-opening of 2-oxazolines with acidic sulfonimide nucleophiles

Gutierrez, David A.,Dean, Dayton R.,Laxamana, Candace M.,Migliozzi-Smith, Madyson,O'Brien, Connor J.,O'Neill, Claire L.,Li, Jie Jack

, p. 261 - 276 (2016/07/06)

Acidic sulfonimide nucleophiles includin...

CuCl-catalyzed radical cyclisation of N-α-perchloroacyl-ketene-N,S- acetals: A new way to prepare disubstituted maleic anhydrides

Cornia, Andrea,Felluga, Fulvia,Frenna, Vincenzo,Ghelfi, Franco,Parsons, Andrew F.,Pattarozzi, Mariella,Roncaglia, Fabrizio,Spinelli, Domenico

experimental part, p. 5863 - 5881 (2012/09/22)

The copper-catalyzed radical cyclization...

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...

10431-98-8 Process route

ethanolamine
141-43-5

ethanolamine

Triethyl orthopropionate
115-80-0

Triethyl orthopropionate

2-ethyl-4,5-dihydrooxazole
10431-98-8

2-ethyl-4,5-dihydrooxazole

Conditions
Conditions Yield
With acetic acid; at 105 ℃; for 24h; Inert atmosphere;
75%
ethanolamine
141-43-5

ethanolamine

propionic acid
802294-64-0,79-09-4

propionic acid

2-ethyl-4,5-dihydrooxazole
10431-98-8

2-ethyl-4,5-dihydrooxazole

Conditions
Conditions Yield
ethanolamine; propionic acid; at 180 - 200 ℃; for 3 - 4h;
With boric acid; In toluene; at 130 ℃;
With calcium oxide; at 280 ℃; for 3h;
92%
for 24h; Heating;

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    ethanolamine

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    propionic acid

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