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Merck

137448

2-Methyl-2-oxazoline

98%

Sinónimos:

2-Methyloxazoline

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Fórmula empírica (notación de Hill):
C4H7NO
Número CAS:
Peso molecular:
85.10
Beilstein/REAXYS Number:
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.

pictograms

Flame

signalword

Danger

hcodes

pcodes

Hazard Classifications

Flam. Liq. 2

Clase de almacenamiento

3 - Flammable liquids

wgk_germany

WGK 3

flash_point_f

68.0 °F - closed cup

flash_point_c

20 °C - closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter


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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
Jing Tong et al.
Molecular pharmaceutics, 10(1), 360-377 (2012-11-21)
Superoxide dismutase 1 (SOD1) efficiently catalyzes dismutation of superoxide, but its poor delivery to the target sites in the body, such as brain, hinders its use as a therapeutic agent for superoxide-associated disorders. Here to enhance the delivery of SOD1
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
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
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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