2-(Methacryloyloxy)ethyl 1,3-Dioxo-1,3-dihydroisobenzofuran-5-carboxylate

Product Information

Molecular Formula:
C15H12O7
Molecular Weight:
304.25
Description
Reactive monomer, especially in dental applications. Used as adhesion promoter.
Synonyms
1,3-dioxo-5-isobenzofurancarboxylic acid 2-(2-methyl-1-oxoprop-2-enoxy)ethyl ester; 2-(2-methylprop-2-enoyloxy)ethyl 1,3-dioxo-2-benzofuran-5-carboxylate
IUPAC Name
2-(2-methylprop-2-enoyloxy)ethyl 1,3-dioxo-2-benzofuran-5-carboxylate
Canonical SMILES
CC(=C)C(=O)OCCOC(=O)C1=CC2=C(C=C1)C(=O)OC2=O
InChI
InChI=1S/C15H12O7/c1-8(2)12(16)20-5-6-21-13(17)9-3-4-10-11(7-9)15(19)22-14(10)18/h3-4,7H,1,5-6H2,2H3
InChI Key
RMCCONIRBZIDTH-UHFFFAOYSA-N
Boiling Point
553.6 °C at 760 mmHg
Melting Point
95 °C
Purity
98 %
Density
1.374 g/cm3
Storage
Protect from moisture; Store at 4 °C
LogP
1.27330

Safety Information

Hazards
Unknown
Precautionary Statement
P261, P264, P270, P272, P280, P301+P312, P302+P352, P305+P351+P338, P321, P330, P332+P313, P333+P313, P337+P313, P362, P363, and P501
Signal Word
Warning

QC Data

Computed Properties

XLogP3
2
Hydrogen Bond Donor Count
0
Hydrogen Bond Acceptor Count
7
Rotatable Bond Count
7
Exact Mass
304.05830272 g/mol
Monoisotopic Mass
304.05830272 g/mol
Topological Polar Surface Area
96Ų
Heavy Atom Count
22
Formal Charge
0
Complexity
522
Isotope Atom Count
0
Defined Atom Stereocenter Count
0
Undefined Atom Stereocenter Count
0
Defined Bond Stereocenter Count
0
Undefined Bond Stereocenter Count
0
Covalently-Bonded Unit Count
1
Compound Is Canonicalized
Yes

Patents

Publication Number Title Priority Date
CN-113221531-A Multi-model dynamic collaborative semantic matching method 2021-06-04
CN-113372870-A Special adhesive for aluminum plastic film and preparation method thereof 2021-05-26
CN-113372870-B Special adhesive for aluminum plastic film and preparation method thereof 2021-05-26
CN-113304054-A Dental self-acid-etching adhesive with remineralization effect and preparation method thereof 2021-05-25
CN-113304057-A Dental composition and preparation method thereof 2021-05-19
CN-112940204-A Preparation method of polybutadiene latex for agglomeration and prepared ABS resin 2021-02-04
CN-113332486-A Adhesive composition for hard tissue repair and kit for hard tissue repair 2021-01-09
KR-102260473-B1 Flowable resin with low polymerization shrinkage and Manufacturing method of the same 2021-01-06
CN-112515974-A Self-adhesive resin cement composition for dentistry 2020-12-11
CN-112717196-A Adhesive composition for repairing hard tissue 2020-12-11

Literatures

PMID Publication Date Title Journal
22623052 2012-10-01 Effects of calcium salts of acidic monomers on mineral induction of phosphoprotein immobilized to agarose beads Journal of biomedical materials research. Part A
22282759 2012-08-01 Dentin bonding performance and ability of four MMA-based adhesive resins to prevent demineralization along the hybrid layer The journal of adhesive dentistry
22734756 2012-06-01 Fourier transform infrared photoacoustic spectroscopy study of physicochemical interaction between human dentin and etch-&-rinse adhesives in a simulated moist bond technique Journal of biomedical optics
22178629 2012-05-01 Effects of primer containing silane and thiophosphate monomers on bonding resin to a leucite-reinforced ceramic Journal of dentistry
21350865 2012-04-01 Effect of curing mode on the micro-mechanical properties of dual-cured self-adhesive resin cements Clinical oral investigations
23037839 2012-01-01 Shear bond strength between autopolymerizing acrylic resin and Co-Cr alloy using different primers Dental materials journal
21924196 2011-10-01 An alternative adhesive strategy to optimize bonding to root dentin Journal of endodontics
21787493 2011-06-01 An in vitro evaluation of the growth of human periodontal ligament fibroblasts after exposure to a 4-META-containing methacrylate-based endodontic sealer Journal of endodontics
21271328 2011-01-01 Early bond strength of two resin cements to Y-TZP ceramic using MPS or MPS/4-META silanes Odontology
21946477 2011-01-01 Effect of functional monomers in all-in-one adhesive systems on formation of enamel/dentin acid-base resistant zone Dental materials journal
The molarity calculator equation

Mass (g) = Concentration (mol/L) × Volume (L) × Molecular Weight (g/mol)

The dilution calculator equation

Concentration (start) × Volume (start) = Concentration (final) × Volume (final)

This equation is commonly abbreviated as: C1V1 = C2V2

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