2633-67-2

Basic information

• Product Name: P-STYRENESULFONYL CHLORIDE
• Synonyms: 4-VINYLBENZENESULFONYL CHLORIDE;4-STYRENE SULFONYL CHLORIDE;P-STYRENESULFONYL CHLORIDE;p-Styrenesulfonyl Chloride (stabilized with TBC);styrene-4-sulfonyl chloride;4-Ethenylbenzenesulfonic acid chloride;4-Vinylbenzene-1-sulfonic acid chloride;p-Styrenesulfonic acid chloride
• CAS NO: 2633-67-2
• Molecular Formula: C₈H₇ClO₂S
• Molecular Weight: 202.66
• EINECS: 404-770-2
• Mol File: 2633-67-2.mol
• Article Data: 51

Chemical Properties

• Melting Point: 86 °C
• Boiling Point: 130 °C / 4mmHg
• Flash Point: 132.4°C
• Appearance: /
• Density: 1.32
• Vapor Pressure: 0.003mmHg at 25°C
• Refractive Index: 1.564
• Storage Temp.: Freezer
• CAS DataBase Reference: P-STYRENESULFONYL CHLORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: P-STYRENESULFONYL CHLORIDE(2633-67-2)
• EPA Substance Registry System: P-STYRENESULFONYL CHLORIDE(2633-67-2)

Safety Data

• Hazard Codes: Xi
• Statements: 34-43-41-38
• Safety Statements: 26-36/37/39-45-37/39-24
• RIDADR: 3265
• Hazardous Substances Data: 2633-67-2(Hazardous Substances Data)

Usage

General Description

P-Styrenesulfonyl chloride is a chemical compound with the formula C8H7ClO2S. It is a reactive compound used in organic synthesis as a building block for the creation of various styrenesulfonyl derivatives. P-STYRENESULFONYL CHLORIDE is widely utilized in the pharmaceutical and agrochemical industries for the synthesis of various drugs and pesticides. P-Styrenesulfonyl chloride is also used in the development of polymer materials and as a reagent in chemical research. It is a highly reactive compound that should be handled with caution due to its potential for causing skin and eye irritation, as well as respiratory issues if inhaled.

InChI:InChI=1/C8H7ClO2S/c1-2-7-3-5-8(6-4-7)12(9,10)11/h2-6H,1H2

Upstream product

• 98-70-4 styrene-4-sulfonic acid 
• 304675-74-9 p-vinylbenzenesulfonic acid sodium hydrate 
• 79-37-8 oxalyl dichloride 
• 2695-37-6 sodium 4-styrenesulfonate 
• 7719-09-7 thionyl chloride 
• 101-54-2 N-phenylphenylene-1,4-diamine 

Downstream Products

• 193340-25-9 (1R,2S,3R,4S)-3-(4-vinylbenzenesulfonyl)amino-1,7,7-trimethylbicyclo[2.2.1]heptan-2-ol 
• 200557-69-3 (1S,2S)-N-(4-vinylphenylsulfonyl)-1,2-diphenylethylenediamine 
• 193810-42-3 (R)-3-Methyl-2-(4-vinyl-benzenesulfonylamino)-butyric acid tert-butyl ester 
• 203639-90-1 (R)-3-Phenyl-2-(4-vinyl-benzenesulfonylamino)-propionic acid tert-butyl ester 
• 203639-59-2 (R)-3-(1H-Indol-3-yl)-2-(4-vinyl-benzenesulfonylamino)-propionic acid methyl ester 
• 2633-64-9 4-vinylbenzenesulfonamide 
• 302584-86-7 (1S,2S,3R,5S)-2-hydroxy-3-pinanyl p-styrenesulfonate 
• 211869-56-6 (1R,2S)-2-(4-vinylbenzenesulfonyl)amino-1-phenylpropan-1-ol 
• 211869-58-8 (1S,2R)-2-(4-vinylbenzenesulfonyl)amino-1-phenylpropan-1-ol 

Relevant articles and documents

Enantioselective addition of organozinc reagents to ketones catalyzed by grafted isoborneolsulfonamide polymers and titanium isopropoxide

The catalytic enantioselective addition of different organozinc reagents, such as diethylzinc, or in situ generated phenylzinc derivatives to simple aryl methyl ketones was accomplished using titanium tetraisopropoxide and a polymeric ligand grafted with

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Latent reactive groups unveiled through equilibrium dynamics and exemplified in crosslinking during film formation from aqueous polymer colloids

The concept of using equilibrium dynamics to provide for both protection and unveiling of latent functional groups at appropriate times in aqueous polymer colloid coatings designed for crosslinking only during film formation is introduced; the new functional monomer, 4-hydroxyethylsulfonylstyrene (HESS), readily undergoes emulsion copolymerization with acrylates to form stable latexes, followed by crosslinking by loss of water during film formation. The Royal Society of Chemistry 2005.

NEW POLYMERS AND THE USE THEREOF FOR DETECTING ION FLUXES

Disclosed are ion-sensitive polymers and methods for their use for monitoring biological phenomena associated with ion fluxes, as well as organic electrochemical transistors including such polymers.

Scalable and Recyclable All-Organic Colloidal Cascade Catalysts

We report on the synthesis of core–shell microparticles (CSMs) with an acid catalyst in the core and a base catalyst in the shell by surfactant-free emulsion polymerization (SFEP). The organocatalytic monomers were separately copolymerized in three synthetic steps allowing the spatial separation of incompatible acid and base catalysts within the CSMs. Importantly, a protected and thermo-decomposable sulfonate monomer was used as acid source to circumvent the neutralization of the base catalyst during shell formation, which was key to obtain stable, catalytically active CSMs. The catalysts showed excellent performance in an established one-pot model cascade reaction in various solvents (including water), which involved an acid-catalyzed deacetalization followed by a base-catalyzed Knoevenagel condensation. The CSMs are easily recycled, modified, and their synthesis is scalable, making them promising candidates for organocatalytic applications.

Synthesis method of N-trifluoromethanesulfonyl-P-styrene sulfonyl imide lithium

The invention discloses a synthesis method of N - trifluoromethylsulfonyl-p-styrene sulfonyl imide lithium, relates to the technical field of battery electrolyte additives, and the synthesis method takes sodium styrene sulfonate and oxalyl chloride under