14674-80-7

Usage

Uses

Used in Polymer Production:
Ethyl acrylate is used as a monomer in the production of polymers for various applications, such as adhesives, sealants, and textile coatings. Its reactive nature allows it to be easily polymerized, making it a valuable component in the manufacturing process.
Used in Adhesives and Sealants:
Ethyl acrylate is used as a component in the formulation of adhesives and sealants due to its ability to form strong bonds and its compatibility with various substrates.
Used in Textile Coatings:
Ethyl acrylate is used in the production of textile coatings to provide durability, water resistance, and other desirable properties to fabrics.
Used in Coatings:
Ethyl acrylate is used in the formulation of coatings for various surfaces, such as automotive and industrial coatings, to provide protection, durability, and aesthetic appeal.
Used in Manufacturing Industry:
Ethyl acrylate is used as a raw material in the manufacturing industry for the production of various products, including plastics, rubber, and other synthetic materials.
It is important to handle and dispose of ethyl acrylate with caution due to its flammability and potential health hazards, such as skin and eye irritation, respiratory issues, and gastrointestinal problems if inhaled or ingested.

Upstream product

• 6191-99-7 (2E)-3-ethoxyprop-2-enoyl chloride 
• 5941-55-9 ethyl 3-ethoxyacrylate 
• 64-17-5 ethanol 
• 54299-82-0 C₉H₁₇NO₂ 
• 16339-88-1 (E)-1-bromo-2-ethoxyethene 
• 124-38-9 carbon dioxide 
• 59938-07-7 (3E)-1,1,1-trichloro-4-ethoxybut-3-en-2-one 
• 59938-06-6 (E)-4-Ethoxy-1,1,1-trifluoro-3-buten-2-one 
• 19483-24-0 cis-β-Ethoxyacrylsaeure 

Downstream Products

• 773138-32-2 2-hydroxy-benzene-1,3,5-tricarboxylic acid triethyl ester 
• 6191-99-7 (2E)-3-ethoxyprop-2-enoyl chloride 
• 1621424-10-9 benzyl (E)-3-ethoxyacrylate 
• 6191-99-7 3-ethoxyacryloyl chloride 
• 115983-78-3 (E)-3-ethoxypropenoyl isocyanate 
• 928627-14-9 trans-N-(3-bromo-2-methoxyphenyl)-3-ethoxy-2-propenamide 
• 923973-02-8 (E)-N-(1-(2,6-dichlorophenyl)-4-methyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl)-3-ethoxyacrylamide 

Relevant academic research and scientific papers

INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE

Compounds of formula (I') and methods of their use and preparation, as well as compositions comprising compounds of formula (I').

INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE

The present disclosure is directed to compounds of formula I and methods of their use and preparation, as well as compositions comprising compounds of formula I.

2-Ethoxyvinyllithiums and diethoxyvinyllithiums: What makes them stable or fragile?

The elusive (E)-2-ethoxyvinyllithium can be readily generated in tetrahydrofuran at -75 °C from (E)-1-bromo-2-ethoxyethylene by halogen/metal exchange and subsequently trapped with electrophiles. Alkylation opens a convenient entry to (E)-configurated enethers. (E)-2-Ethoxyvinyllithium decomposes rapidly at -50 °C whereas its (Z)-isomer, which lacks the possibility to eliminate lithium ethoxide in a favorable anti-periplanar process, is stable under the same conditions. (E)-1,2-Diethoxyvinyllithium even sustains reflux temperatures (approximately 75 °C). 2,2-Diethoxyvinyllithium and (Z)-1,2-diethoxyvinyllithium can be conserved at 0 °C although this time loss of alcoholate can occur in the anti-mode. Obviously it matters whether the energy-rich ethoxyacetylene is formed as the elimination product or simple acetylene, as in the case of (E)-2-ethoxyvinyllithium.

Haloacetylated Enol Ethers. 8 [12]. Reaction of β-Alkoxyvinyl Trihalomethyl Ketones with Guanidine Hydrochloride. Synthesis of 4-Trihalomethyl-2-Aminopyrimidines

In this work the results of the reaction of β-alkoxyvinyl trihalomethyl ketones 1, 2a-e, with guanidine hydrochloride are reported. Depending on the ketone 1 or 2 and the conditions under which the reactions were carried out, 4-trihalomethyl-2-amino pyrimidines, β-alkoxyvinyl carboxylic acids, or β-acetal carboxylic esters were obtained.

Electroorganic Synthesis, 56. Synthesis of Advanced Prostaglandin Precursors by Kolbe Electrolysis, I. - Preparation of (1'R,4'S,3R/S)-3-(cis-4-Acetoxycyclopent-2-enyloxy)-3-ethoxypropionic Acid

The key intermediate of a novel synthesis of prostaglandin precursors, (1'R,4'S,3R/S)-3-(cis-4-acetoxycyclopent-2-enyloxy)-3-ethoxypropionic acid (3), is prepared by two different synthetic sequences: In a first strategy transacetalization of ethyl 3,3-diethoxypropionate (6) with (1R,4S)-4-acetoxy-1-hydroxy-2-cyclopentene (7) leads to the formation of the mixed acetal 8.By subsequent hydrolysis and acylation 8 could be converted into acid 3 in six steps in 6percent overall yield.However, the generation of acid 3 by bromoalkoxidation of 3-ethoxyacrylates 13d, e and subsequent electrochemical reduction proved to be more efficient.In this reduction it is possible to debrominate the α-bromo esters 14d, e and to remove the 2-haloethyl ester group in one step.Using this reaction sequence, we could synthesize acid 3 in five steps in 38percent overall yield. - Key Words: Kolbe electrolysis / Radical cyclization / Electrochemical dehalogenation / Prostaglandins

A Convenient Synthetic Method for β-Alkoxy- and β-Phenoxyacrylic Acids and 3,4-Dihydro-2H-pyran-5- and 2,3-Dihydrofuran-4-carboxylic Acids

trans-β-Trihaloacetylvinyl ethers 1 are easily hydrolyzed by wet potassium hydroxide in benzene, yielding the corresponding acids 2 in excellent yields.This synthetic method also can be applicable to cyclic vinyl ethers 3 and 5 to yield 4 and 6 in high yi