14674-80-7 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.
Check Digit Verification of cas no
The CAS Registry Mumber 14674-80-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,6,7 and 4 respectively; the second part has 2 digits, 8 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 14674-80:
(7*1)+(6*4)+(5*6)+(4*7)+(3*4)+(2*8)+(1*0)=117
117 % 10 = 7
So 14674-80-7 is a valid CAS Registry Number.
14674-80-7Relevant articles and documents
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Ficini,J.,Depezay,J.-C.
, p. 937 - 942 (1968)
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INHIBITORS OF BRUTON'S TYROSINE KINASE AND METHODS OF THEIR USE
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Page/Page column 334, (2017/09/02)
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?
Schlosser, Manfred,Wei, Heng-Xu
, p. 1735 - 1742 (2007/10/03)
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.
