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N-Ethylmethacrylamide, with the molecular formula C6H11NO2, is a colorless liquid chemical compound. It is utilized as a monomer in the synthesis of various copolymers and is predominantly employed in the production of hydrogels.
Used in Pharmaceutical Industry:
N-Ethylmethacrylamide is used as a component in the creation of hydrogels for drug delivery systems. These hydrogels, due to their high water content, offer a controlled and sustained release of pharmaceuticals, enhancing the efficacy and safety of drug administration.
Used in Tissue Engineering:
In the field of tissue engineering, N-Ethylmethacrylamide is used as a constituent of hydrogels that serve as scaffolds for cell growth and tissue regeneration. The hydrophilic nature of these hydrogels facilitates cell adhesion and proliferation, making them ideal for tissue repair and organ reconstruction.
Used in Ophthalmic Industry:
N-Ethylmethacrylamide is used as a material in the development of contact lenses. The hydrogel-based lenses provide comfort and moisture retention, ensuring better oxygen permeability and hydration for the eyes.
Used in Coatings and Adhesives Industry:
N-ETHYLMETHACRYLAMIDE is also used as a monomer in the production of specialty coatings and adhesives. The resulting polymers offer improved adhesion, flexibility, and durability, making them suitable for various industrial applications.
Used in Textile Industry:
N-Ethylmethacrylamide is utilized in the textile industry for the development of innovative fabrics and fibers. The polymers derived from N-ETHYLMETHACRYLAMIDE can enhance the properties of textiles, such as water absorption, breathability, and softness.
Despite its wide range of applications, N-Ethylmethacrylamide is considered to be relatively low in toxicity. However, caution is advised as exposure to high concentrations may result in irritation to the skin, eyes, and respiratory system.

7370-88-9

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7370-88-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7370-88-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,7 and 0 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 7370-88:
(6*7)+(5*3)+(4*7)+(3*0)+(2*8)+(1*8)=109
109 % 10 = 9
So 7370-88-9 is a valid CAS Registry Number.
InChI:InChI=1/C6H11NO/c1-4-7-6(8)5(2)3/h2,4H2,1,3H3,(H,7,8)

7370-88-9SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N-ethyl-2-methylprop-2-enamide

1.2 Other means of identification

Product number -
Other names 2-Propenamide,N-ethyl-2-methyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7370-88-9 SDS

7370-88-9Relevant academic research and scientific papers

Effect of Transition Metals on Chemodivergent Cross-Coupling of Acrylamides with Vinyl Acetate via C-H Activation

Logeswaran, Ravichandran,Jeganmohan, Masilamani

supporting information, p. 5679 - 5683 (2021/08/03)

A novel chemodivergent cross-coupling of acrylamides and vinyl acetates has been realized via metal-catalyzed vinylic C-H activation. The selective olefinic C-H vinylation and alkenylation reaction was examined with a variety of differently functionalized acrylamides. The reaction efficiently generates a range of highly synthetically valuable butadienes with good functional group tolerance in good to moderate yields. A possible catalytic reaction mechanism involving the chelation-assisted olefinic C-H activation via an acetate-assisted deprotonation pathway is proposed.

TRISUBSTITUTED FUROPYRIMIDINES AND USE THEREOF

-

Page/Page column 18-19, (2010/11/03)

The invention relates to the novel 4,5,6-trisubstituted furo[2,3-d]pyrimidine derivatives of formula (I), to methods for their production, their use in the treatment and/or prophylaxis of diseases and their use in the production of drugs for the treatment

N-alkylation of methacrylamide with alkyl halides

Shirshin,Kazantsev,Kazakov,Danov

, p. 1418 - 1420 (2007/10/03)

N-Alkylation of methacrylamide with ethyl bromide, ethyl iodide, and allyl bromide in acetonitrile in the presence of alkalis yields N- and N,N-substituted methacrylamides. The effect of temperature, reactant ratio, nature of the alkyl halide, and water content on the reaction course was studied.

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