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7784-80-7

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7784-80-7 Usage

General Description

2-Allyloxyethyl acrylate is a chemical compound with the molecular formula C9H14O3. It is a colorless to pale yellow liquid with a pungent odor and is often used in the production of polymers and resins. This chemical is commonly used in the manufacturing of adhesives, coatings, and inks due to its ability to crosslink and form durable bonds. Additionally, 2-allyloxyethyl acrylate is also utilized as a reactive diluent in UV-curable coatings and in the production of specialty plastics. However, it may pose some health hazards and should be handled with care, as it can cause skin and eye irritation and may be harmful if inhaled or ingested.

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

7784-80-7SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-prop-2-enoxyethyl prop-2-enoate

1.2 Other means of identification

Product number -
Other names 2-Allyloxyethylacrylate

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7784-80-7 SDS

7784-80-7Downstream Products

7784-80-7Relevant articles and documents

Synthesis and characterization of network type single ion conductors

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.

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