22121-86-4 Usage
Description
Ethyl 2-ethoxy acrylate is a clear, colorless liquid with a faint, fruity odor, commonly used as a versatile monomer in the production of coatings, adhesives, and sealants. It can polymerize to form a variety of polymers with different properties, making it useful in a wide range of applications. However, it is highly flammable and should be handled with care due to its potential health hazards, including skin and eye irritation, and harmful effects if inhaled or ingested.
Uses
Used in Coatings Industry:
Ethyl 2-ethoxy acrylate is used as a monomer for the production of coatings, providing a variety of polymers with different properties to meet specific application requirements.
Used in Adhesives Industry:
Ethyl 2-ethoxy acrylate is used as a monomer for the production of adhesives, offering a wide range of polymers with varying properties to suit different bonding needs.
Used in Sealants Industry:
Ethyl 2-ethoxy acrylate is used as a monomer for the production of sealants, enabling the creation of polymers with diverse properties to cater to various sealing applications.
Used as a Solvent:
Ethyl 2-ethoxy acrylate is used as a solvent in various industrial processes, providing a clear, colorless liquid with a faint, fruity odor for use in different applications.
Used as a Chemical Intermediate:
Ethyl 2-ethoxy acrylate is used as a chemical intermediate in the production of other compounds, contributing to the synthesis of various chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 22121-86-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,1,2 and 1 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 22121-86:
(7*2)+(6*2)+(5*1)+(4*2)+(3*1)+(2*8)+(1*6)=64
64 % 10 = 4
So 22121-86-4 is a valid CAS Registry Number.
22121-86-4Relevant articles and documents
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Monnin
, p. 1983,1987 (1957)
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A tandem "on-palladium" Heck-Jeffery amination route toward the synthesis of functionalized indole-2-carboxylates
McNulty, James,Keskar, Kunal
supporting information; experimental part, p. 6902 - 6908 (2012/01/02)
A direct synthesis of functionalized indole-2-carboxylates involving a PdII-catalyzed annulation of ortho-iodoanilines onto a vinyl ether is described. The reaction mechanism is shown to be distinct from a stepwise Heck, intramolecular amination pathway, likely involving a tandem "on-palladium" Heck-Jeffery amination process incorporating a novel intramolecular amination step.
Intramolecular 4+3 cycloadditions, vinylthionium ions from allylic alcohols
Harmata,Jones
, p. 783 - 786 (2007/10/03)
Aldehyde 9 can be prepared from ethyl pyruvate in several steps. Treatment of 1 with various diene-containing Grignard reagents results in the formation of the corresponding allylic alcohol in good yield. Exposure of these alcohols to triflic anhydride results in the formation of 4+3 cycloadducts in good to excellent yields. Furan and simple butadiene trap the intermediate allylic cation efficiently in the formation of 5,7-fused ring systems. A tethered thiophene undergoes only intramolecular Friedel-Crafts alkylation.
