7700-07-4

Usage

Uses

Used in Pharmaceutical Industry:
Ethenesulfonic acid dimethylamide is used as an intermediate in the synthesis of pharmaceuticals for its ability to participate in various chemical reactions, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical sector, Ethenesulfonic acid dimethylamide serves as an intermediate in the production of agrochemicals, aiding in the creation of compounds that enhance crop protection and yield.
Used in Dye Industry:
Ethenesulfonic acid dimethylamide is utilized as an intermediate in the manufacturing of dyes, enabling the production of a wide range of colorants for various applications.
Used as a Reactive Solvent:
Due to its strong acidic nature, Ethenesulfonic acid dimethylamide is employed as a reactive solvent in various chemical processes, facilitating reactions that require an acidic environment.
Used as a Curing Agent for Epoxy Resins:
Ethenesulfonic acid dimethylamide is used as a curing agent for epoxy resins, promoting the hardening and cross-linking of these resins, which is crucial in the manufacturing of composite materials and coatings.
Used as a Stabilizer for Chlorinated Solvents:
This chemical compound also functions as a stabilizer for chlorinated solvents, enhancing their performance and extending their shelf life in various industrial applications.
It is crucial to handle and store Ethenesulfonic acid dimethylamide with proper safety measures, as it can be harmful if ingested, inhaled, or absorbed through the skin.

InChI:InChI=1/C4H9NO2S/c1-4-8(6,7)5(2)3/h4H,1H2,2-3H3

Upstream product

• 1622-32-8 2-Chloroethanesulfonyl chloride 
• 124-40-3 dimethyl amine 
• 6608-47-5 vinylsulfonyl chloride 

Downstream Products

• 1346254-71-4 C₁₀H₁₄ClNO₂S 
• 1093849-60-5 C₁₀H₁₅NO₂S 
• 1235382-50-9 benzyl 4-{2-[(dimethylamino)sulfonyl]ethoxy}piperidine-1-carboxylate 

Relevant academic research and scientific papers

Metal-free visible-light-promoted C(sp3)-H functionalization of aliphatic cyclic ethers using trace O2

Presented is a light-promoted C-C bond forming reaction yielding sulfone and phosphate derivatives at room temperature in the absence of metals or photoredox catalyst. This transformation proceeds in neat conditions through an auto-oxidation mechanism which is maintained through the leaching of trace amounts of O2 as sole green oxidant. This journal is

The first examples of rhodium-catalyzed 1,4-conjugate addition reactions of arylboronic acids with ethenesulfonamides

An unprecedented rhodium-catalyzed 1,4-conjugate addition of arylboronic acids with ethenesulfonamides resulting in the corresponding 2-arylethanesulfonamides is described. The amino substituent, the applied arylboronic acid, the type of Rh-catalyst, and the experimental conditions all affected the reaction outcome.

Process for synthesis of optically pure prostaglandin E2 and analogs thereof

The invention comprises a multi-step synthesis of l(-) prostaglandin E2. The special features of the synthesis include: (1) a triply-convergent conjugate-addition and alkylation reaction involving the 1,4-addition of a chiral vinyl lithium reagent to a chiral vinylsulfone to produce a sulfone-stabilized anion. This anion is alkylated in situ to produce the basic prostaglandin skeleton structure, which is then subjected to (2) an efficient peracid oxidation of a secondary amine to a β-silyloxy oxime; and (3) an alkali-catalyzed 1,4-elimination of an α-sulfonyl oxime to produce a vinyl nitroso intermediate. This intermediate is treated with borohydride to give a stereospecific 1,4-reduction which yields the bis-silyloxy oxime of l(-)PGE2. Hydrolysis of the oxime, with concurrent cleavage of the silyloxy protecting groups, affords l(-)PGE2.