2426-54-2 Usage
Uses
Used in Polymer Production:
2-(Diethylamino)-ethyl acrylate is used as a monomer in the production of polymers for its ability to contribute to the formation of polymer chains with specific properties, such as flexibility and reactivity.
Used in Chemical Synthesis:
It serves as a chemical intermediate in the synthesis of other compounds, facilitating the creation of a wide range of products through its reactive functional groups.
Used in Adhesives Manufacturing:
2-(Diethylamino)-ethyl acrylate is used as a component in the manufacturing of adhesives, where its reactivity and bonding capabilities enhance the adhesive's performance and durability.
Used in Coatings Industry:
In the coatings industry, it is utilized to improve the properties of coatings, such as adhesion, flexibility, and resistance to environmental factors, by incorporating it into the formulation of various types of coatings.
Used in Textile Industry:
2-(Diethylamino)-ethyl acrylate is used in the textile industry to modify the properties of fibers and fabrics, enhancing their performance characteristics, such as strength, flexibility, and resistance to wear and tear.
It is crucial to handle 2-(Diethylamino)-ethyl acrylate with care, considering its potential to cause skin and eye irritation and harmful effects if ingested or inhaled. Adhering to proper safety measures and protocols is essential when working with this chemical compound.
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.
A new method using 2-chloro-4,6-dimethoxy-1,3,5-triazine for facile elimination of dimethylamino group in Eschenmoser's methylenation for synthesis of α,β-unsaturated esters
Yamada, Kohei,Masaki, Kazumasa,Hagimoto, Yuri,Kamiya, Seina,Kunishima, Munetaka
supporting information, p. 1758 - 1760 (2013/03/29)
A facile one-step method for the elimination of the dimethylamino group in Eschenmoser's methylenation has been developed using a combination of 2-chloro-4,6-dimethoxy-1,3,5-triazine and triethylamine. The chemoselective elimination of the dimethylamino group occurred in compounds possessing either a diethylamino group or an alkylsulfanyl group.
