25781-90-2

Usage

Uses

Used in Organic Synthesis:
Benzenamine,4-(ethenylsulfonyl)is used as a key intermediate in organic synthesis for the creation of a variety of different compounds. Its unique chemical structure allows for numerous reactions and transformations, making it a valuable component in the synthesis of complex organic molecules.
Used in Pharmaceutical Production:
In the pharmaceutical industry, Benzenamine,4-(ethenylsulfonyl)is utilized in the production of various drugs and medicinal compounds. Its reactivity and functional groups enable the development of new pharmaceuticals with potential therapeutic benefits.
Used in Dye Manufacturing:
Benzenamine,4-(ethenylsulfonyl)is also employed in the manufacturing of dyes, where its chemical properties contribute to the color and stability of the final product. Its use in this industry highlights its versatility and importance in different sectors.
Used in Other Industrial Applications:
Beyond the mentioned industries, Benzenamine,4-(ethenylsulfonyl)finds use in various other applications, further demonstrating its significance in the realm of organic chemistry and industrial processes. Its adaptability and reactivity make it a valuable asset in the development and production of a wide array of products.

InChI:InChI=1/C8H9NO2S/c1-2-12(10,11)8-5-3-7(9)4-6-8/h2-6H,1,9H2

Upstream product

• 26732-14-9 acetic acid-(4-ethenesulfonyl-anilide) 
• 5246-58-2 4-(2'-Hydroxyethylsulphonyl)aniline 
• 100-00-5 4-chlorobenzonitrile 
• 5535-55-7 1-nitro-4-(vinylsulfonyl)benzene 
• 21386-32-3 p-nitrophenyl-β-hydroxyethylsulfone 
• 295782-27-3 acetic acid-[4-(2-iodo-ethanesulfonyl)-anilide] 

Downstream Products

• 1001079-45-3 2-(2-(4-aminophenylsulfonyl)ethylamino)ethanol 
• 25442-63-1 4-(2-diethylamino-ethanesulfonyl)-aniline 
• 1123208-63-8 C₁₈H₂₅N₃O₇S₃ 
• 1123208-58-1 C₁₇H₂₃N₃O₄S₂ 
• 1123208-68-3 C₁₀H₁₆N₂O₂S 
• 1123208-55-8 N,N-di-[2-(4'-aminophenyl)-sulphonylethyl]-amine 
• 1123208-56-9 C₁₈H₂₅N₃O₄S₂ 
• 90643-77-9 4-(2-methoxyethylsulfonyl)benzenamine 

Relevant academic research and scientific papers

DYE AND DYEING METHOD

A dyeing method is provided, which includes dyeing a dye to a fiber by a supercritical fluid, wherein the dye has a chemical structure of:R 1 is C1-6alkyl group, R 2 is C1-6alkyl group, each of R 3 is independently of H or C1-6alkyl group, and R 4 is a single bond or C1-6alkylene group. When R 4 is single bond, R 5 is. When R 4 is C1-6alkylene group, R 5 is H, Br, Cl, or. Each of R 6 is independently of H, Cl, Br, OCH3, or C1-6alkyl group.

Dye compounds and resin composition for color filter comprising the same

The present invention relates to a pyridone azo dye compound for a color filter resin composition having excellent solubility and heat resistance, which is represented by the following chemical formula 1 and contains an acrylic group or a meta-acrylic group. The pyridone azo dye compound according to the present invention has excellent solubility and heat resistance with respect to an organic solvent, thereby having higher solubility as a coloring agent of the color filter resin composition than a pigment; and maximizing coloring performance and realizing high color reproducibility by reducing an amount of an additive added for pigment dispersion stability. [Chemical formula 1]COPYRIGHT KIPO 2016

Aza-Michael reactions with vinyl sulfones and Amberlyst-15 as catalyst

Vinyl p-aminophenylsulfone and methyl vinyl sulfone were shown to react, as Michael acceptors, with a broad range of secondary and primary amines using Amberlyst as catalyst. The reactions occurred, generally, with high yields and in a short time.