137448
2-Methyl-2-oxazoline
98%
Synonym(s):
2-Methyloxazoline
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About This Item
Empirical Formula (Hill Notation):
C4H7NO
CAS Number:
Molecular Weight:
85.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
214-316-3
Beilstein/REAXYS Number:
104227
MDL number:
Assay:
98%
Form:
liquid
InChI key
GUXJXWKCUUWCLX-UHFFFAOYSA-N
InChI
1S/C4H7NO/c1-4-5-2-3-6-4/h2-3H2,1H3
SMILES string
CC1=NCCO1
assay
98%
form
liquid
Quality Level
bp
109.5-110.5 °C (lit.)
density
1.005 g/mL at 25 °C (lit.)
Related Categories
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.
Application
2-Methyl-2-oxazoline was used in cationic polymerization of a series of linear 2-alkyl-2-oxazolines under microwave irradiation.
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Yalin Zhang et al.
Talanta, 150, 375-387 (2016-02-04)
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Pavel Sťahel et al.
Polymers, 11(12) (2019-12-18)
Polyoxazolines are a new promising class of polymers for biomedical applications. Antibiofouling polyoxazoline coatings can suppress bacterial colonization of medical devices, which can cause infections to patients. However, the creation of oxazoline-based films using conventional methods is difficult. This study
Jing Tong et al.
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Ke Mao et al.
Talanta, 168, 230-239 (2017-04-11)
In this work, a one-step coating procedure by a simple annealing protocol of poly (2-methyl-2-oxazoline)-random-glycidyl methacrylate (PMOXA-r-GMA) copolymer was used to yield covalent and cross-linked PMOXA-based antifouling coating on a fused-silica capillary inner surface, which was used to determine the
Laetitia Korchia et al.
Soft matter, 13(25), 4507-4519 (2017-06-07)
A series of amphiphilic photo-responsive heterografted copolymers have been successfully synthesized. The random copolymers were composed of a methacrylate backbone, with various compositions of hydrophilic oligomeric 2-methyl-2-oxazoline side chains (OMOx) and hydrophobic long alkyl chains terminated by a coumarin moiety
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