14674-80-7

Basic information

• Product Name: 2-Propenoicacid, 3-ethoxy-, (2E)-
• Synonyms: (E)-3-Ethoxyacrylic acid;2-Propenoicacid, 3-ethoxy-, (E)-;Acrylic acid, 3-ethoxy-, (E)- (8CI);(E)-3-Ethoxy-2-propenoic acid;(2E)-3-Ethoxyprop-2-enoic acid
• CAS NO: 14674-80-7
• Molecular Formula: C₅H₈O₃
• Molecular Weight: 116.117
• Mol File: 14674-80-7.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 217.6 °C at 760 mmHg
• Flash Point: 92.9 °C
• Density: 1.098 g/cm³
• CAS DataBase Reference: 2-Propenoicacid, 3-ethoxy-, (2E)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoicacid, 3-ethoxy-, (2E)-(14674-80-7)
• EPA Substance Registry System: 2-Propenoicacid, 3-ethoxy-, (2E)-(14674-80-7)

Safety Data

• Hazardous Substances Data: 14674-80-7(Hazardous Substances Data)

Usage

Description

2-Propenoic acid, 3-ethoxy-, (2E)-, also known as ethyl acrylate, is a colorless liquid with a pungent, fruity odor and the molecular formula C5H8O2. It is a chemical compound often used in the production of polymers and coatings, and is highly flammable and toxic to aquatic life.

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

• 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 
• 64-17-5 ethanol 
• 54299-82-0 C₉H₁₇NO₂ 
• 5941-55-9 ethyl 3-ethoxyacrylate 
• 6191-99-7 (2E)-3-ethoxyprop-2-enoyl chloride 

Downstream Products

• 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 
• 6191-99-7 (2E)-3-ethoxyprop-2-enoyl chloride 
• 773138-32-2 2-hydroxy-benzene-1,3,5-tricarboxylic acid triethyl ester 

Relevant articles and documents

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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.

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.