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)
Nitrogen-rich melamine (66% by mass) had been found to be illegally adulterated to milk products and animal feed in order to increase the apparent protein content, and ingestion of melamine may lead to the formation of kidney stones. Hence, the
Yunjiao Che et al.
Soft matter, 16(29), 6733-6742 (2020-06-27)
We report a novel double cross-linked hydrogel system based on polyacrylamide and poly(2-methyl-2-oxazoline) (PMOXA) network chains, as well as on supramolecular host-guest interactions with on-demand tailored mechanical properties. Well-defined vinyl-bearing PMOXA macromonomers, functionalized with either β-cyclodextrin units (β-CD-PMOXA) or adamantane
Ondrej Sedlacek et al.
Journal of controlled release : official journal of the Controlled Release Society, 326, 53-62 (2020-06-23)
Poly(2-oxazoline)s represent an emerging class of polymers with increasing potential in biomedical sciences. To date, most of the work on poly(2-oxazoline)-drug conjugates focused on poly(2-ethyl-2-oxazoline) (PEtOx), a biocompatible water-soluble polymer with biological properties similar to polyethylene glycol. However, the more
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
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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