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

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

Uses

Used in Pharmaceutical Industry:
P-Styrenesulfonyl chloride is used as a key intermediate in the synthesis of various drugs. Its reactivity allows for the development of new pharmaceutical compounds with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical sector, P-Styrenesulfonyl chloride serves as a crucial component in the production of pesticides. Its ability to form various derivatives makes it valuable for creating effective pest control agents.
Used in Polymer Material Development:
P-Styrenesulfonyl chloride is utilized in the development of polymer materials, contributing to the creation of novel polymers with unique properties and applications in various industries.
Used as a Reagent in Chemical Research:
As a highly reactive compound, P-Styrenesulfonyl chloride is employed as a reagent in chemical research, enabling scientists to explore new chemical reactions and synthesize innovative compounds for various applications.

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

Upstream product

• 2695-37-6 sodium 4-styrenesulfonate 
• 79-37-8 oxalyl dichloride 
• 304675-74-9 p-vinylbenzenesulfonic acid sodium hydrate 
• 98-70-4 styrene-4-sulfonic acid 
• 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 
• 2633-64-9 4-vinylbenzenesulfonamide 
• 211869-56-6 (1R,2S)-2-(4-vinylbenzenesulfonyl)amino-1-phenylpropan-1-ol 
• 890127-34-1 (1R,2R)-N₁-(4-vinylbenzenesulfonyl)-1,2-diphenylethane-1,2-diamine 
• 874096-49-8 N-(p-vinylbenzenesulfonyl)-(S)-tryptophan 
• 853894-04-9 (2S)-N-((1S,2R)-1-benzyl-2-hydroxy-3-{isobutyl[(4-vinylphenyl)sulfonyl]amino}propyl)-3-methyl-2-{3-[(2-methyl-1,3-thiazol-4-yl)methyl]-2-oxo-1-imidazolidinyl}butanamide 

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

Influence of Chain Rigidity and Dielectric Constant on the Glass Transition Temperature in Polymerized Ionic Liquids

Polymerized ionic liquids (PolyILs) are promising candidates for a wide range of technological applications due to their single ion conductivity and good mechanical properties. Tuning the glass transition temperature (Tg) in these materials con

Molded, high surface area polymer electrolyte membranes from cured liquid precursors

Polymer electrolyte membranes (PEMs) for fuel cells have been synthesized from easily processable, 100% curable, low molecular weight reactive liquid precursors that are photochemically cured into highly proton conductive solid membranes. The liquid precu

Synthesis, Characterization, and Biological Investigation of Alanine-Based Sulfonamide Derivative: FT-IR, 1H NMR Spectra: MEP, HOMO–LUMO Analysis, and Molecular Docking

Abstract: A combined experimental and theoretical investigation has been reported on N-(alanine)-p-styrene sulfonamide (abbreviated as ASS). The new title compound have been synthesized for the first time from the reaction of p-styrene sulfonyl chloride a

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.

Realisation of ORMOSIL ionomers by the crosslinking of propyl methacrylate siloxane and a protected styrenesulfonic acid

1,2,3,4-Tetrahydro-1-naphthylideneamino styrene-p-sulfonate (NISS) and poly(propyl methacrylate siloxane) (PMS) were free-radically crosslinked, yielding insoluble copolymers in which the siloxane and NISS components appear well intermixed. These material

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.

Method of manufacturing a polymerizable functional group having a sulfonimide salts

[Problem] high-sulfonimide acids without passing through self-polymerization, to cause halogen residual amine salt as a raw material without using a radiosensitive, simple, high yield, high purity industrial scale production method of adsorbing silver hal

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.

Highly selective electroreductive linear dimerization of electron-deficient vinylarenes

A direct electroreductive dimerization of electron-deficient vinylarenes for the synthesis of 1,4-diarylbutane has been developed using a simple undivided cell with inexpensive carbon electrodes at room temperature. The control and deuterium-labeling experiments of electroreductive dimerization suggest that the hydrogen source comes from the solvent CH3CN. This protocol provides a mild and efficient route for the construction of C–C bond in moderate to good yields with high regioselectivity and broad substrate scope.