40630-40-8

Usage

Uses

Used in Organic Synthesis:
2-(trifluoromethyl)sulfonylaminoethanol is used as a reagent in organic synthesis for its high reactivity and stability. It serves as a key intermediate in the preparation of complex organic molecules, contributing to the development of new chemical entities.
Used in Pharmaceutical Compound Preparation:
In the pharmaceutical industry, 2-(trifluoromethyl)sulfonylaminoethanol is used as a building block for the preparation of various pharmaceutical compounds. Its unique structure allows for the creation of new drug candidates with potential therapeutic applications, making it an essential component in drug discovery and development processes.

Upstream product

• 96-49-1 [1,3]-dioxolan-2-one 
• 421-85-2 Trifluoromethanesulfonamide 
• 358-23-6 trifluoromethylsulfonic anhydride 
• 141-43-5 ethanolamine 
• 421-83-0 trifluoromethane sulfonyl chloride 
• 314756-98-4 2-(methacryloyloxy)ethyltrifluoromethanesulfonamide 

Downstream Products

• 314756-98-4 2-(methacryloyloxy)ethyltrifluoromethanesulfonamide 
• 1373359-69-3 triphenylsulfonium N-[2-(adamantane-1-ylcarbonyloxy)ethyl]trifluoromethanesulfonamide 

Relevant academic research and scientific papers

Trifluoromethanesulfonyl alkyne amide compound as well as preparation method and application thereof

The invention discloses a trifluoromethanesulfonyl alkyne amide compound as well as a preparation method and application thereof. Based on hydrosulfide reaction of the alkyne amide and sulfydryl, selective modification and marking of sulfydryl in polypept

Composition

PURPOSE: Salts are provided to enable use as an acid generator and to obtain a photoresist composition capable of obtaining resist patterns with excellent resolution and shape. CONSTITUTION: Salts are represented by chemical formula I. In chemical formula I, Q^1 and Q^2 are independently fluorine atom or C1-6 perfluoroalkyl group; L^1 is a single bond or divalent C1-17 saturated hydrocarbon which may have substituents, wherein at least one -CH2- included in the saturated hydrocarbon group may be substituted with -O- or CO-; R^1 is C1-6 alkyl group containing a fluorine atom; and Z^+ is organic cation.

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.