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Benzene, [1-[(methylsulfonyl)methyl]ethenyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

80283-74-5

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80283-74-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 80283-74-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,2,8 and 3 respectively; the second part has 2 digits, 7 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80283-74:
(7*8)+(6*0)+(5*2)+(4*8)+(3*3)+(2*7)+(1*4)=125
125 % 10 = 5
So 80283-74-5 is a valid CAS Registry Number.

80283-74-5Downstream Products

80283-74-5Relevant academic research and scientific papers

Copper-Catalyzed Decarboxylative Functionalization of Conjugated β, Γ-Unsaturated Carboxylic Acids

Zhang, Wei,Wang, Chengming,Wang, Qiu

, p. 13179 - 13185 (2020/11/17)

Copper-catalyzed decarboxylative coupling reactions of conjugated β,γ-unsaturated carboxylic acids have been achieved for allylic amination, alkylation, sulfonylation, and phosphinoylation. This approach was effective for a broad scope of amino, alkyl, su

Regiocontrolled synthesis of α-sulfonylmethyl o-nitrostyrenes via ZnI2-mediated sulfonylation and AgNO2/Pd(PPh3)4-promoted o-nitration

Chang, Meng-Yang,Chen, Han-Yu,Wang, Heui-Sin

, p. 10601 - 10610 (2018/05/31)

We report herein the AgNO2/Pd(PPh3)4-promoted regiocontrolled o-nitration of α-sulfonylmethylstyrenes in MeNO2 with good yields. The o-nitration process provides a series of sulfonyl o-nitrostyrenes. Substituted α-sulfonylmethylstyrenes were synthesized from ZnI2-mediated sulfonylation of substituted α-methylstyrenes and sodium sulfinates (RSO2Na) in MeCN with good to excellent yields. The structures of the key products were confirmed by X-ray crystallography. A plausible mechanism has been proposed herein.

Sulfonylative alkoxyhydroxylation of 2-arylpropenes

Wang, Huei-Sin,Wu, Yan-Shin,Chang, Meng-Yang

, p. 6465 - 6470 (2017/10/10)

One-pot three-step sulfonylative alkoxyhydroxylation of 2-arylpropenes 1 affords oxygenated sulfonylcumenes 4 in moderate yields via a sequential route: (i) NBS-mediated allylic bromination of 2-arylpropenes 1 in CH2Cl2, (ii) sodium sulfinates 2-promoted nucleophilic substitution of the resulting styryl bromides in a co-solvent of alcohol and water, and (iii) V2O5/H2O2 mediated alkoxyhydroxylation of corresponding styryl sulfones 3 in alcohol. The synthetic route provides a highly effective protocol for the 1,2,3-tricarbofunctionalization of 2-arylpropenes 1 via two carbon-oxygen and one carbon-sulfur bond formations.

Visible-light induced oxidant-free oxidative cross-coupling for constructing allylic sulfones from olefins and sulfinic acids

Zhang, Guoting,Zhang, Lingling,Yi, Hong,Luo, Yi,Qi, Xiaotian,Tung, Chen-Ho,Wu, Li-Zhu,Lei, Aiwen

supporting information, p. 10407 - 10410 (2016/09/02)

An oxidant-free dehydrogenative sulfonylation of α-methyl-styrene derivatives was developed for the construction of allylic sulfones by using eosin Y as a photosensitizer in conjunction with a cobaloxime catalyst. The process features a low-cost metal catalyst and atom economy, which provides an appealing strategy for future synthetic chemistry.

SYNTHESIS AND ALKYLATION OF VINYLSULFINIC ACIDS VIA FLUORIDE CLEAVAGE OF β-TRIMETHYLSILYLETHYL VINYL SULFONES

Palmer, James T.,Fuchs, P. L.

, p. 233 - 246 (2007/10/02)

A new method for the synthesis of vinylsulfinic acids from aldehydes is described.The homologated vinyl (trimethylsilylethyl)sulfones were synthesized from the corresponding aldehydes by means of the phosphonium salt derived from the chloromethylsulfide o

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