3-Ethyl-3-(methacryloyloxy)methyloxetane CAS#: 37674-57-0; ChemWhat Code: 1411590

IdentificationPhysical DataSpectra
Route of Synthesis (ROS)Safety and HazardsOther Data

Identification

Product Name3-Ethyl-3-(methacryloyloxy)methyloxetane
IUPAC Name(3-ethyloxetan-3-yl)methyl 2-methylprop-2-enoate 
Molecular Structurestructure of 3-Ethyl-3-(methacryloyloxy)methyloxetane CAS 37674-57-0
CAS Registry Number 37674-57-0
MDL NumberMFCD16039335
Synonyms37674-57-0
(3-Ethyloxetan-3-yl)methyl methacrylate
3-Ethyl-3-(Methacryloyloxy)Methyloxetane
(3-ethyloxetan-3-yl)methyl 2-methylprop-2-enoate
2-Propenoic acid, 2-methyl-, (3-ethyl-3-oxetanyl)methyl ester
(3-Ethyloxetan-3-yl)methylmethacrylate
SCHEMBL156498
DTXSID10457203
3-ethyl-3-methacryloxymethyloxetane
MFCD16039335
3-ethyl-3-oxetanylmethyl methacrylate
3-ethyl-3-methacryloyloxymethyloxetane
AKOS016010268
DS-5784
PB47763
(1-ethyl-3-oxacyclobutyl)methyl methacrylate
E1379
O10082
A874034
Molecular FormulaC10H16O3
Molecular Weight184.23
InChI InChI=1S/C10H16O3/c1-4-10(5-12-6-10)7-13-9(11)8(2)3/h2,4-7H2,1,3H3  
InChI KeyRSHKWPIEJYAPCL-UHFFFAOYSA-N 
Canonical SMILESCCC1(COC1)COC(=O)C(=C)C
Patent Information
Patent IDTitlePublication Date
US2012/45616POSITIVE PHOTOSENSITIVE RESIN COMPOSITION, METHOD FOR FORMING CURED FILM, CURED FILM, ORGANIC EL DISPLAY DEVICE AND LIQUID CRYSTAL DISPLAY DEVICE2012

Physical Data

AppearanceColorless clear liquid

Spectra

No data available


Route of Synthesis (ROS)

Route of Synthesis (ROS) of 3-Ethyl-3-(methacryloyloxy)methyloxetane CAS 37674-57-0

ConditionsYield
With 2,2′-azobis-(2,4-dimethylvaleronitrile) In 3-methoxy butanol; 3-methoxybutyl acetate at 90℃; for 8h;
Experimental Procedure
Example 15; The inside of a 1-liter flask equipped with a reflux condenser, dropping funnels, and a stirrer was allowed to be a nitrogen atmosphere by feeding a suitable amount of nitrogen thereto; 150 parts by weight of 3-methoxy-1-butanol and 110 parts by weight of 3-methoxybutyl acetate were placed in the flask and heated to 90°C with stirring. Next, a solution was prepared by dissolving 60 parts by weight of methacrylic acid (MAA), 160 parts by weight of a 50:50 (by mole) mixture (E-DCPA) of 3,4-epoxytricyclo[5.2.1.02,6]dec-9-yl acrylate (belonging to compounds represented by Formula (1a-1)) and 3,4-epoxytricyclo[5.2.1.02,6]dec-8-yl acrylate (belonging to compounds represented by Formula (1a-2)), and 80 parts by weight of (3-ethyl-3-oxetanyl)methyl methacrylate (OXMA) in 170 parts by weight of 3-methoxybutyl acetate. The solution was added dropwise into the flask using a dropping pump over about three hours. Separately, 50 parts by weight of 2,2′-azobis(2,4-dimethylvaleronitrile) as a polymerization initiator was dissolved in 220 parts by weight of 3-methoxybutyl acetate to yield a solution, and this solution was added dropwise into the flask using another dropping pump over about five hours. After the completion of dropwise addition of the polymerization initiator, the mixture was held at the same temperature for about three hours, then cooled to room temperature, and thereby yielded a copolymer solution having a viscosity at 23°C of 98 mPa.s, a solid content of 31.5 percent by weight, and an acid value as a solution of 36.3 mg-KOH/g. The formed copolymer had a weight-average molecular weight (Mw) of 8700 and a molecular weight distribution of 2.06.

Safety and Hazards

No data available


Other Data

TransportationNot dangerous goods
HS Code
StorageStore at room temperature, sealed and away from light.
Shelf Life2 years
Market Price
Druglikeness
Lipinski rules component
Molecular Weight184.235
logP1.51
HBA3
HBD0
Matching Lipinski Rules4
Veber rules component
Polar Surface Area (PSA)35.53
Rotatable Bond (RotB)5
Matching Veber Rules2
Use Pattern
3-Ethyl-3-(methacryloyloxy)methyloxetane CAS #: 37674-57-0 is a commonly used photoinitiator that can undergo copolymerization with other monomers such as methyl methacrylate and acrylic esters to form high molecular weight polymers. These polymers exhibit excellent optical properties and abrasion resistance, making them widely used in coatings, adhesives, and optical materials.
UV-curable coatings prepared from 3-Ethyl-3-(methacryloyloxy)methyloxetane can rapidly cure under ultraviolet (UV) irradiation. These coatings offer good adhesion, abrasion resistance, and chemical resistance, making them suitable for coating surfaces such as wood, plastics, and metals.

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Warshel Chemical Ltdhttp://www.warshel.com/
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