2633-64-9

Usage

Uses

Used in Pharmaceutical Industry:
P-Sulfonamido styrene is used as a key intermediate for the synthesis of various pharmaceutical compounds due to its unique reactivity and properties, contributing to the development of new drugs with improved therapeutic effects.
Used in Agrochemical Industry:
P-Sulfonamido styrene serves as an important building block in the production of agrochemicals, such as pesticides and herbicides, leveraging its reactivity to create effective and targeted agricultural solutions.
Used in Polymer and Resin Production:
P-Sulfonamido styrene is utilized as a monomer for the synthesis of specialty polymers with enhanced thermal and mechanical properties, improving the performance of materials used in various industries.
Used in Synthetic Rubber Industry:
P-Sulfonamido styrene acts as a crosslinking agent in the production of synthetic rubber, enhancing the rubber's strength, durability, and resistance to wear and tear.
Used in Polymer Materials:
P-Sulfonamido styrene is employed in the development of polymer materials with specific properties, such as improved thermal stability and mechanical strength, for use in various applications across different industries.

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

Upstream product

• 5378-84-7 4-(2-bromoethyl)-benzenesulfonamide 
• 5378-85-8 2-(4-Aminosulfonylphenyl)ethyl chloride 
• 2633-67-2 4-vinylbenzenesulfonyl chloride 
• 108-05-4 vinyl acetate 
• 701-34-8 4-bromo-benzenesulfonic acid amide 
• 622-24-2 2-phenylethyl chloride 
• 4796-23-0 4-(2-chloro-ethyl)-benzenesulfonyl chloride 
• 2695-37-6 sodium 4-styrenesulfonate 

Downstream Products

• 1565-37-3 4-(1,2-dibromo-ethyl)-benzenesulfonic acid amide 
• 91557-74-3 1-Propyl-3-(p-vinylbenzolsulfonyl)thioharnstoff 
• 94906-33-9 1-Phenyl-3-(p-vinylbenzolsulfonyl)harnstoff 
• 92959-50-7 1-Allyl-3-(p-vinylbenzolsulfonyl)thioharnstoff 
• 92033-41-5 1-Butyl-3-(p-vinylbenzolsulfonyl)thioharnstoff 
• 92034-04-3 1-(p-Vinylbenzolsulfonyl)-3-t-butyl-harnstoff 
• 260782-77-2 (E,E,E)-1,6-bis[(2,4,6-triisopropylphenyl)sulfonyl]-11-[(4-vinylphenyl)sulfonyl]-1,6,11-triazacyclopentadeca-3,8,13-triene 

Relevant academic research and scientific papers

Single lithium-ion conducting polymer electrolytes based on a super-delocalized polyanion

A novel single lithium-ion (Li-ion) conducting polymer electrolyte is presented that is composed of the lithium salt of a polyanion, poly[(4-styrenesulfonyl)(trifluoromethyl(S-trifluoromethylsulfonylimino)sulfonyl)imide] (PSsTFSI-), and high-mo

Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Vinyl Acetate in Dimethyl Isosorbide as a Sustainable Solvent

A nickel-catalyzed reductive cross-coupling has been achieved using (hetero)aryl bromides and vinyl acetate as the coupling partners. This mild, applicable method provides a reliable access to a variety of vinyl arenes, heteroarenes, and benzoheterocycles, which should expand the chemical space of precursors to fine chemicals and polymers. Importantly, a sustainable solvent, dimethyl isosorbide, is used, making this protocol more attractive from the point of view of green chemistry.

BIS-(4-HALOETHYLBENZENESULFONYL)IMIDE OR ITS SALT, METHOD FOR PRODUCING THE SAME AND METHOD FOR PRODUCING BIS-(4-STYRENESULFONYL)IMIDE OR ITS SALT USING BIS-(4-HALOETHYLBENZENESULFONYL)IMIDE AS PRECURSOR

PROBLEM TO BE SOLVED: To provide a method for producing bis-(4-styrenesulfonyl)imide or its salt which is excellent in radical polymerizability, cation exchangeability and high water-solubility and is extremely useful for producing an ion exchange membran

BIS-(4-HALOETHYLBENZENESULFONYL)IMIDE OR ITS SALT, METHOD FOR PRODUCING THE SAME AND METHOD FOR PRODUCING BIS-(4-STYRENESULFONYL)IMIDE OR ITS SALT USING BIS-(4-HALOETHYLBENZENESULFONYL)IMIDE AS PRECURSOR

PROBLEM TO BE SOLVED: To provide bis-(4-styrenesulfonyl)imide or its salt which is a crosslinkable monomer having excellent radical polymerizability, cation exchangeability and high water-solubility and is extremely useful for producing a solid electrolyt

COMPOUND INCLUDING AROMATIC RING, POLYMER INCLUDING THE SAME

The present disclosure relates to a compound including an aromatic ring and to a polymer including the same. The compound according to one embodiment of the present invention has a styrene-based functional group capable of radical polymerization and a fun

NOVEL CROSS-LINKER FOR THE PREPARATION OF A NEW FAMILY OF SINGLE ION CONDUCTION POLYMERS FOR ELECTROCHEMICAL DEVICES AND SUCH POLYMERS

A specific cross-linker, an alkaline metal bis(styrenesulfonyl)imide monomer, is used in the synthesis of single ionic conductive copolymers that are non-fluorinated and non-PEO based. Such copolymers meet the security and costs requirements to be used as

NOVEL CROSS-LINKER FOR THE PREPARATION OF A NEW FAMILY OF SINGLE ION CONDUCTION POLYMERS FOR ELECTROCHEMICAL DEVICES AND SUCH POLYMERS

A specific cross-linker, an alkaline metal bis(styrenesulfonyl)imide monomer, is used in the synthesis of single ionic conductive copolymers that are non-fluorinated and non-PEO based. Such copolymers meet the security and costs requirements to be used as

Oxidation reactions using polymer-supported 2-benzenesulfonyl-3-(4- nitrophenyl)oxaziridine

A thermally stable polymer-supported oxidant has been developed. Polymer-supported 2-benzenesulfonyl-3-(4-nitrophenyl)oxaziridine was applied to microwave-assisted reactions that occurred at high temperatures and was shown to oxidize alkenes, silyl enol ethers, and pyridines to the corresponding epoxides and pyridine N-oxides in excellent to good yields and with much shorter reaction times. It also enabled tetrahydrobenzimidazoles to be oxidatively rearranged to spiro fused 5-imidazolones in a more efficient manner. Recycling of the polymer-supported oxidant is also possible with minimal loss of activity after several reoxidations.

The first example of molecularly imprinted nanogels with aldolase type I activity

The molecular-imprinting approach was used to obtain a nanogel preparation capable of catalysing the cross-aldol reaction between 4-nitrobenzaldehyde and acetone. A polymerisable proline derivative was used as the functional monomer to mimic the enamine-b

Facile regeneration of carbonyl compounds from oximes using poly[4-vinyl-N,N-dichlorobenzenesulfonamide]

Oximes of aldehydes and ketones are oxidized to the corresponding carbonyl compounds in good yields under mild conditions by poly[4-vinyl-N,N-dichlorobenzenesulfonamide].