40807-05-4

Usage

Uses

Used in Organic Synthesis:
(E)-2-(3-nitrophenyl)ethenyl phenyl sulfone is utilized as a reagent in organic synthesis, where its capacity to engage in various chemical reactions is highly beneficial. Its versatility in this context allows for the creation of a wide array of products, contributing to the compound's significance in the field.
Used in Pharmaceutical Development:
The unique structure and properties of (E)-2-(3-nitrophenyl)ethenyl phenyl sulfone render it a promising candidate for the development of pharmaceuticals. Its ability to undergo multiple chemical reactions enables the synthesis of a variety of compounds with potential therapeutic applications.
Used in Agrochemical Production:
In addition to its pharmaceutical applications, (E)-2-(3-nitrophenyl)ethenyl phenyl sulfone is also employed in the production of agrochemicals. Its chemical reactivity and structural uniqueness make it a valuable component in the development of new and improved products for the agricultural industry.
Used in the Construction of Functional Materials:
(E)-2-(3-nitrophenyl)ethenyl phenyl sulfone serves as a building block for the construction of various functional materials. Its chemical properties and reactivity contribute to the creation of materials with specific characteristics, making it a valuable resource in material science and engineering.

Upstream product

• 683-08-9 Diethyl methylphosphonate 
• 368-43-4 phenylsulfonyl fluoride 
• 99-61-6 3-nitro-benzaldehyde 
• 586-39-0 1-nitro-3-vinyl-benzene 
• 873-55-2 sodium benzenesulfonate 
• 5535-48-8 PVS 
• 13331-27-6 m-nitrobenzene boronic acid 
• 555-68-0 m-Nitrocinnamic Acid 
• 80-17-1 benzenesufonyl hydrazide 
• 579-71-5 2-nitrostyrene 
• 1212-08-4 S-Phenyl benzenethiosulfonate 
• 3959-23-7 benzenesulfonylacetic acid 

Relevant academic research and scientific papers

Method for synthesizing (E)-(2-(phenylsulfonyl)vinyl)benzene and derivative thereof

The invention provides a method for synthesizing (E)-(2-(phenylsulfonyl)vinyl)benzene and a derivative thereof. The method adopts styrene or a derivative of styrene as a reactant A and sodium benzenesulfinate or a derivative of sodium benzenesulfinate as

Synthesis of Vinyl Sulfones via I2-mediated Alkene Sulfonylations with Thiosulfonates

A simple sulfonylation strategy involving I2 and thiosulfonates, as sulfonyl-group precursors, is reported for the synthesis of vinyl sulfones. Sulfonyl radicals are presumed to be generated from thiosulfonates, which subsequently react with st

Visible-Light-Enabled Decarboxylative Sulfonylation of Cinnamic Acids with Sulfonylhydrazides under Transition-Metal-Free Conditions

Decarboxylative cross-coupling reactions of cinnamic acids with sulfonylhydrazides were explored using oxygen as the sole terminal oxidant, realizing a conceptually novel technology for vinyl sulfone synthesis under the synergistic interactions of visible light irradiation, organic dye-type photocatalyst eosin Y, KI, and Cs2CO3 at room temperature.

An improved synthesis of vinyl- and β-iodovinyl sulfones by a molecular iodine-mediated one-pot iodosulfonationdehydroiodination reaction

An improved one-pot method to synthesize vinyl sulfones from unsaturated systems by using molecular iodine/sodium arenesulfinate/sodium acetate as reagents was described. Vinyl sulfones derived from styrene derivatives were generally obtained in good to excellent yields except for those bearing strong electron releasing substituent. Aliphatic alkenes and activated alkenes gave the corresponding vinyl sulfone products in moderate to good yields. Arylacetylenes yielded the respective β-iodovinyl sulfones in good yields while low yield was observed with aliphatic terminal alkyne. The potentials of the method entail simplicity, short reaction time, non-anhydrous reaction conditions, employing inexpensive, non-metallic reagent and integrating two reactions that are commonly accomplished separately into a single operation. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file. Copyright Taylor & Francis Group, LLC.

Convenient synthesis of α,β-unsaturated sulfones via a Mizoroki-Heck reaction of arylboronic acids with phenyl vinyl sulfones

Palladium acetate catalyzed Mizoroki-Heck reaction of arylboronic acids with phenyl vinyl sulfones afford α,β-unsaturated sulfones in good yields.

CAN mediated reaction of aryl sulfinates with alkenes and alkynes: Synthesis of vinyl sulfones, β-iodovinyl sulfones and acetylenic sulfones

Cerium(IV) ammonium nitrate (CAN) mediated reaction of aryl sulfinates and sodium iodide with alkenes afforded vinyl sulfones in very good yields. Alkynes underwent similar reaction to give β-iodovinyl sulfones, which on treatment with potassium carbonate

Direct sulfonylation of lithiated alkyl phosphonates with benzenesulfonyl fluoride; Facile method for preparation of α-sulfonyl alkyl phosphonates and vinyl sulfones

α-Sulfonyl phosphonates were synthesized by direct sulfonylation of lithiated alkyl phosphonates with benzenesulfonyl fluoride which have shown different reactivity from benzenesulfonyl chloride, generally known as a sulfonylating reagent.