7784-80-7 Usage
Uses
Used in Polymer and Resin Production:
2-Allyloxyethyl acrylate is used as a monomer in the production of polymers and resins for its ability to crosslink and form strong, durable bonds, enhancing the performance and stability of the final products.
Used in Adhesives:
In the adhesives industry, 2-Allyloxyethyl acrylate is used as a component to improve the bonding strength and durability of adhesive formulations, making them suitable for a wide range of applications, including automotive, construction, and packaging.
Used in Coatings:
2-Allyloxyethyl acrylate is used as a reactive diluent in UV-curable coatings, contributing to the rapid curing process and providing excellent adhesion, gloss, and chemical resistance to the coatings.
Used in Inks:
In the ink industry, 2-Allyloxyethyl acrylate is used to enhance the performance of ink formulations, improving their adhesion to various substrates and providing resistance to water, chemicals, and abrasion.
Used in Specialty Plastics:
2-Allyloxyethyl acrylate is utilized in the production of specialty plastics, where its crosslinking properties contribute to the development of materials with unique properties, such as high heat resistance, chemical resistance, and mechanical strength.
Check Digit Verification of cas no
The CAS Registry Mumber 7784-80-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,7,8 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 7784-80:
(6*7)+(5*7)+(4*8)+(3*4)+(2*8)+(1*0)=137
137 % 10 = 7
So 7784-80-7 is a valid CAS Registry Number.
InChI:InChI=1/C8H12O3/c1-3-5-10-6-7-11-8(9)4-2/h3-4H,1-2,5-7H2
7784-80-7Relevant academic research and scientific papers
Sun, Xiao-Guang,Reeder, Craig L.,Kerr, John B.
, p. 2219 - 2227 (2004)
New single ion conductors were synthesized by grafting the allyl group-containing lithium salt, lithium bis(allylmalonato)borate (LiBAMB), onto allyl group-containing comb-branch polyacrylate or polymethacrylate ethers by means of hydrosilylation. The highest ambient temperature conductivity of 3.5 × 10-7 S cm-1 was obtained for a polyacrylate ether-based single ion conductor containing eight EO units in the side chain and five EO units in the cross-linking side chain, to which the anion was fixed with a salt concentration of EO/Li = 20. For polyacrylate ether-based single ion conductors, an increase of chain length in both side chains and cross-linking anion chains favors an increase of ionic conductivity. The addition of 50 wt % EC/DMC (1/1, wt/wt) increased the ionic conductivity by more than 2 orders of magnitude due to both the increase in ionic mobility from the liquid phase and the increase in the concentration of free ions from the high dielectric constant of the solvent. The preliminary Li/Li cycling profiles of dry polyacrylate- and polymethacrylate ether-based single ion conductors are encouraging as almost no concentration polarization or relaxation was observed. The observed increase in cell potential with cycling is apparently due to an increase in the interfacial impedance associated with the SEI layer, and the cell failure is accompanied by the decomposition of the ester bond of the polyacrylate backbone.
