2426-54-2 Usage
General Description
2-(Diethylamino)-ethyl acrylate is a chemical compound that contains a diethylamino group and an acrylate functional group, which makes it a member of the acrylate ester family. It is used in various industrial applications, including as a monomer in the production of polymers and as a chemical intermediate in the synthesis of other compounds. This chemical is also utilized in the manufacturing of adhesives, coatings, and textiles. It is important to handle 2-(Diethylamino)-ethyl acrylate with caution, as it can be a skin and eye irritant and may have harmful effects if ingested or inhaled. As with any potentially hazardous chemical, proper safety measures and protocols should be followed when working with 2-(Diethylamino)-ethyl acrylate.
Check Digit Verification of cas no
The CAS Registry Mumber 2426-54-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,4,2 and 6 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2426-54:
(6*2)+(5*4)+(4*2)+(3*6)+(2*5)+(1*4)=72
72 % 10 = 2
So 2426-54-2 is a valid CAS Registry Number.
InChI:InChI=1/C9H17NO2/c1-5-9(11)12-8(4)10(6-2)7-3/h5,8H,1,6-7H2,2-4H3
2426-54-2Relevant articles and documents
Synthesis and Antibacterial Activity of Polymerizable Acryloyloxyalkyltriethyl Ammonium Salts
Mancuso, Raffaella,Amuso, Roberta,Armentano, Biagio,Grasso, Giuseppe,Rago, Vittoria,Cappello, Anna Rita,Galiano, Francesco,Figoli, Alberto,De Luca, Giorgio,Hoinkis, Jan,Gabriele, Bartolo
, p. 1235 - 1244 (2017/10/06)
This study reports an efficient and practical synthetic approach for the synthesis of a particularly important class of polymerizable quaternary ammonium salts (PQASs), that is, acryloxyalkyltriethylammonium bromides (AATEABs), which may find application as antimicrobial coatings for commercial membranes with antifouling and anti-biofouling properties, to be used for wastewater treatment. The synthetic method is based on a simple two-step procedure from commercially available substrates, entirely carried out under air and without any need for chromatographic purification. All the newly synthesized AATEABs were tested for their antimicrobial activity, and the results showed that AATEABs bearing an alkyl chain of 11 and particularly 12 carbon atoms possessed significant activity against Gram positive bacteria and yeast strains.
