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
Beilstein:
104227
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
liquid
refractive index
n20/D 1.434 (lit.)
bp
109.5-110.5 °C (lit.)
density
1.005 g/mL at 25 °C (lit.)
SMILES string
CC1=NCCO1
InChI
1S/C4H7NO/c1-4-5-2-3-6-4/h2-3H2,1H3
InChI key
GUXJXWKCUUWCLX-UHFFFAOYSA-N
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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.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Flam. Liq. 2
Storage Class Code
3 - Flammable liquids
WGK
WGK 3
Flash Point(F)
68.0 °F - closed cup
Flash Point(C)
20 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Hoogenboom R, et al.
Designed Monomers and Polymers, 8(6), 659-671 (2005)
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Lignin, one of the most abundant renewable feedstock, is used to develop a biocompatible hydrogel as anti-infective ointment. A hydrophilic polyoxazoline chain is grafted through ring opening polymerization, possess homogeneous spherical nanoparticles of 10-15 nm. The copolymer was covalently modified with
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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
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