687-46-7 Usage
Description
ETHYL ALPHA-CHLOROACRYLATE, also known as chloroethyl acrylate, is a colorless liquid with a pungent odor and is highly reactive due to the presence of the alpha-chloroacrylate group. It is a chemical compound used as a monomer in the production of polymers and acrylic resins.
Used in Adhesives Industry:
ETHYL ALPHA-CHLOROACRYLATE is used as a monomer for the production of polymers and acrylic resins, which are essential components in the manufacturing of adhesives. These adhesives are used in various applications, such as bonding materials together in construction, automotive, and packaging industries.
Used in Coatings Industry:
In the coatings industry, ETHYL ALPHA-CHLOROACRYLATE is used as a monomer to produce polymers and acrylic resins that contribute to the formulation of coatings. These coatings are applied in various sectors, including automotive, architectural, and industrial settings, to provide protection, durability, and aesthetic appeal.
Used in Other Industrial Products:
ETHYL ALPHA-CHLOROACRYLATE is also utilized in the manufacturing of other industrial products, such as textiles, paper, and plastics. Its reactivity and ability to form polymers make it a valuable component in the development of these products, enhancing their properties and performance.
It is crucial to handle ETHYL ALPHA-CHLOROACRYLATE with care, as it is a hazardous substance that can cause skin and eye irritation, as well as respiratory issues if inhaled. Additionally, it is classified as a flammable liquid and should be stored and handled in a well-ventilated area with proper safety measures in place.
Check Digit Verification of cas no
The CAS Registry Mumber 687-46-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,8 and 7 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 687-46:
(5*6)+(4*8)+(3*7)+(2*4)+(1*6)=97
97 % 10 = 7
So 687-46-7 is a valid CAS Registry Number.
InChI:InChI=1/C5H7ClO2/c1-3-8-5(7)4(2)6/h2-3H2,1H3
687-46-7Relevant articles and documents
Synthesis and reactivity of α and β-chloro-α-phenylselanyl esters
Lebarillier, Loic,Outurquin, Francis,Paulmier, Claude
, p. 7495 - 7502 (2007/10/03)
Thermal decomposition of the dichloro-adducts derived from α-phenylselanylesters 1, 2 and 4 has been studied. N-Chloro-succinimide treatment of esters 2 was an efficient preparative method for α-chloro-α-phenylselanylesters 10 and α-chloro-α,β-unsaturated esters 11. Some transformations of esters 10 were achieved, α,β-Dichloro-α-phenylselanylesters 22 were prepared from β-chloro-α-phenylselanylesters 5 or by decomposition of the dichloroselenuranes 21 derived from esters 4. (C) 2000 Elsevier Science Ltd.
