314756-98-4

Basic information

• Product Name: 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester
• Synonyms: 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester
• CAS NO: 314756-98-4
• Molecular Formula: C7H10F3NO4S
• Molecular Weight: 261.2188096
• EINECS: -0
• Mol File: 314756-98-4.mol

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester(314756-98-4)
• EPA Substance Registry System: 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester(314756-98-4)

Safety Data

• Hazardous Substances Data: 314756-98-4(Hazardous Substances Data)

Usage

Uses

Used in Polymer Production:
2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is used as a crosslinking agent in the production of polymers for various applications. Its ability to form covalent bonds between polymer chains enhances the mechanical properties and stability of the resulting materials.
Used in Adhesive Manufacturing:
In the adhesive industry, 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is utilized as a key component in the formulation of high-performance adhesives. Its crosslinking properties contribute to the development of strong, durable, and long-lasting adhesives for various substrates.
Used in Coating Formulation:
2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is used as a crosslinking agent in the formulation of coatings. Its incorporation into coating systems improves the adhesion, durability, and resistance to environmental factors such as UV radiation, moisture, and chemicals.
Used in Paint Production:
In the paint industry, 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is employed as a crosslinking agent to enhance the performance of paint formulations. Its addition to paint systems results in improved adhesion, durability, and resistance to weathering and chemical exposure.
Used in Ink Formulation:
2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is used as a crosslinking agent in the formulation of inks for various printing applications. Its incorporation into ink systems improves the adhesion, durability, and resistance to smudging and fading.
Overall, 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is a valuable chemical compound with diverse applications across various industries. However, its potential hazards necessitate careful handling and proper safety measures to ensure the well-being of workers and the environment.

Upstream product

• 358-23-6 trifluoromethylsulfonic anhydride 
• 2420-94-2 2-aminoethylmethacrylate hydrochloride 
• 335-05-7 Trifluoromethanesulfonyl fluoride 
• 760-93-0 methacryloyl anhydride 
• 40630-40-8 trifluoromethanesulfonamide ethanol 
• 421-83-0 trifluoromethane sulfonyl chloride 

Downstream Products

• 40630-40-8 trifluoromethanesulfonamide ethanol 

Relevant articles and documents

Process for Producing Fluoroalkylsulfonylaminoethyl Alpha-Substituted-Acrylate

Aminoethanol is reacted with a fluoroalkylsulfonic anhydride to obtain a fluoroalkylsulfonylaminoethanol (first step: sulfonylamidation step). The fluoroalkylsulfonylaminoethanol is esterified with an α-substituted acrylate derivative to obtain a desired fluoroalkylsulfonylaminoethyl α-substituted-acrylate (second step: esterification step). Thus, the desired fluoroalkylsulfonylaminoethyl α-substituted-acrylate having a higher purity can be produced in higher yield with higher operating efficiency than in conventional techniques.

Process for Producing Fluorine-Containing Alkylsulfonylaminoethyl Alpha-Substituted Acrylate

There is provided a process for producing a fluorine-containing alkylsulfonylaminoethyl α-substituted acrylate of the formula [3] by reaction of an aminoethyl α-substituted acrylate of the formula [1a] with a fluorine-containing alkylsulfonic fluoride of the formula [2], or by reaction of an aminoethyl a-substituted acrylate salt of the formula [1b] with a fluorine-containing alkylsulfonic fluoride of the formula [2] in the presence of a base, wherein a fluorine-containing compound is used as a reaction solvent: where R1 is a hydrogen atom, methyl group, ethyl group, n-propyl group, isopropyl group, n-butyl group, sec-butyl group, tertbutyl group, fluoromethyl group, difluoromethyl group, trifluoromethyl group or perfluoroethyl group; R2 is a fluorine-containing alkyl group having a carbon number of 1 to 6; Xn? is a counter anion (n is a positive integer); and Y is a fluorine atom, chlorine atom or bromine atom.

Process for producing fluoroalkanesulfonamide derivatives

There is provided a process for producing a fluoroalkanesulfonamide derivative represented by the formula [3], [in-line-formulae]R2—NH—SO2—Rf—R1??[3][/in-line-formulae] including reacting a fluoroalkanesulfonic anhydride represented by the formula [1], with an organic primary amine represented by the formula [2], in the presence of water and in the presence of a base selected from the group consisting of (a) a hydroxide of an alkali metal or alkaline-earth metal or (b) a basic salt containing an alkali metal or alkaline-earth metal.

Process for producing fluorine-containing alkylsulfonylaminoethyl a-substitued acrylate

The present invention provides a process for producing a fluorine-containing alkylsulfonylaminoethyl α-substituted acrylate represented by general formula [3]: which comprises reacting an aminoethyl α-substituted acrylate represented by general formula [1a]or a salt thereof: with a fluorine-containing alkylsulfonyl halide represented by general formula [2a] or a fluorine-containing alkylsulfonic anhydride represented by general formula [2b]: .