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30166-88-2

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30166-88-2 Usage

Description

(E)-2-(4-methylphenyl)ethenyl phenyl sulfone is a chemical compound with the molecular formula C14H12O2S. It is a sulfone compound that consists of a phenyl group attached to a sulfone group and a methylphenyl group attached to an ethenyl group. (E)-2-(4-methylphenyl)ethenyl phenyl sulfone is known for its unique chemical properties and is often utilized in various organic synthesis processes.

Uses

Used in Pharmaceutical Industry:
(E)-2-(4-methylphenyl)ethenyl phenyl sulfone is used as a reagent for the synthesis of various pharmaceuticals. Its unique structure allows it to participate in organic synthesis processes, contributing to the development of new drugs and medications.
Used in Agrochemical Industry:
In the agrochemical industry, (E)-2-(4-methylphenyl)ethenyl phenyl sulfone is used as a reactant in the production of agrochemicals. Its involvement in organic synthesis aids in the creation of compounds that can be used in the development of pesticides, fertilizers, and other agricultural products.
Used in Organic Synthesis:
(E)-2-(4-methylphenyl)ethenyl phenyl sulfone is used as a reactant in the Heck reaction, a palladium-catalyzed coupling reaction for the synthesis of carbon-carbon bonds. This reaction is crucial in the formation of complex organic molecules, which are essential in various chemical and pharmaceutical applications.
Used in Materials Science:
Due to its unique chemical properties, (E)-2-(4-methylphenyl)ethenyl phenyl sulfone may have potential applications in materials science. It could be utilized in the development of new materials with specific properties, such as improved strength, durability, or chemical resistance, depending on the requirements of various industrial processes.

Check Digit Verification of cas no

The CAS Registry Mumber 30166-88-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,0,1,6 and 6 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 30166-88:
(7*3)+(6*0)+(5*1)+(4*6)+(3*6)+(2*8)+(1*8)=92
92 % 10 = 2
So 30166-88-2 is a valid CAS Registry Number.

30166-88-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-[(E)-2-(benzenesulfonyl)ethenyl]-4-methylbenzene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:30166-88-2 SDS

30166-88-2Relevant articles and documents

Controlled Synthesis of β-Keto Sulfones and Vinyl Sulfones under Electrochemical Oxidation

Fang, Yang,Xu, Dongping,Yu, Yingliang,Tang, Rumeng,Dai, Shuaishuai,Wang, Zhenghua,Zhang, Wu

, (2022/04/09)

Selective sulfonylation and oxosulfonylation of alkenes with sulfinates have been developed via anodic oxidation in an undivided cell. The novel electrosynthetic method provided β-keto sulfones and vinyl sulfones with good to excellent yields in the absence of any transition metal catalyst and oxidants. Mechanism studies show that two different pathways involved in these two transformations.

Generation of potent Nrf2 activators via tuning the electrophilicity and steric hindrance of vinyl sulfones for neuroprotection

Song, Zi-Long,Hou, Yanan,Bai, Feifei,Fang, Jianguo

, (2020/12/21)

Oxidative stress is constantly involved in the etiopathogenesis of an ever-widening range of neurodegenerative diseases. As a consequence, effective repression of cellular oxidative stress to a redox homeostatic condition is a promising and feasible strategy to treat, or at least retard the progression of, such disorders. Nrf2, a primary orchestrator of cellular antioxidant response machine, is responsible for detoxifying and compensating for deleterious oxidative stress via transcriptional activation of a diverse array of antioxidant biomolecules. In the framework of our persistent interest in disclosing small molecules that interfere with cellular redox-regulating machinery, we report herein the synthesis, optimization, and biological assessment of 47 vinyl sulfone scaffold-bearing small molecules, most of which exhibit robust neuroprotective effect against H2O2-mediated lesions to PC12 cells. After initial screening, the most potent neuroprotective compounds 9b and 9c with marginal cytotoxicity were selected for the follow-up studies. Our results demonstrate that their neuroprotective effects are attributed to the up-regulation of a panel of antioxidant genes and corresponding gene products. Further mechanistic studies indicate that Nrf2 is indispensable for the cellular performances of 9b and 9c, arising from the fact that silence of Nrf2 gene drastically nullifies their protective action. Taken together, 9b and 9c discovered in this work merit further development as neuroprotective candidates for the treatment of oxidative stress-mediated pathological conditions.

Intermolecular [2 + 2] Photocycloaddition of α,β-Unsaturated Sulfones: Catalyst-Free Reaction and Catalytic Variants

Jeremias, Noah,Mohr, Lisa-Marie,Bach, Thorsten

supporting information, p. 5674 - 5678 (2021/08/03)

2-Aryl-1-sulfonyl-substituted cyclobutanes were prepared in an intermolecular [2 + 2] photocycloaddition from various α,β-unsaturated sulfones and olefins upon irradiation at λ = 300 nm (26 examples, 60-99% yield). Lewis acids catalyzed the [2 + 2] photocycloaddition of 2-benzimidazolyl styryl sulfones. At short wavelengths, the latter substrates underwent C-S bond cleavage but AlBr3 (5 mol %) allowed for an intermolecular reaction with 2,3-dimethyl-2-butene at longer wavelengths. A chiral-at-metal Lewis acid (2 mol %) facilitated an enantioselective reaction (up to 77% ee).

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