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
• Article Data: 4

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

General Description

2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is a compound that is also known as methyl-2-(trifluoromethylsulfonyl)aminoethyl acrylate. It is a chemical used in the production of polymers and adhesives as it can act as a crosslinking agent. It is also used in the manufacturing of coatings, paints, and inks. 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is a colorless liquid with a sharp, pungent odor and is considered to be hazardous if it comes into contact with skin or if it is inhaled. Overall, 2-Propenoic acid, 2-Methyl-, 2-[[(trifluoroMethyl)sulfonyl]aMino]ethyl ester is a versatile chemical that has various industrial applications but should be handled with caution due to its potential hazards.

Upstream product

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

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 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.