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N-(2,2-dimethylpent-4-en-1-yl)-4-methoxybenzenesulfonamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

958870-22-9

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958870-22-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 958870-22-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,5,8,8,7 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 958870-22:
(8*9)+(7*5)+(6*8)+(5*8)+(4*7)+(3*0)+(2*2)+(1*2)=229
229 % 10 = 9
So 958870-22-9 is a valid CAS Registry Number.

958870-22-9Downstream Products

958870-22-9Relevant academic research and scientific papers

Copper-Catalyzed Carbonylative Synthesis of β-Homoprolines from N-Fluoro-sulfonamides

Wu, Xiao-Feng,Yin, Zhiping,Zhang, Youcan

supporting information, p. 1889 - 1893 (2020/03/24)

A new methodology for the carbonylative transformation of N-fluoro-sulfonamides into N-sulfonyl-β-homoproline esters has been described. In the presence of a catalytic amount of Cu(OTf)2, a range of β-homoproline derivatives were prepared in moderate to good yield. The reaction proceeds via the intramolecular cyclization and intermolecular carbonylation of a free carbon radical. Notably, this procedure offers the possibility to build potential functionalized bioactive molecules.

Intermolecular Anti-Markovnikov Hydroamination of Unactivated Alkenes with Sulfonamides Enabled by Proton-Coupled Electron Transfer

Zhu, Qilei,Graff, David E.,Knowles, Robert R.

supporting information, p. 741 - 747 (2018/01/26)

Here we report a catalytic method for the intermolecular anti-Markovnikov hydroamination of unactivated alkenes using primary and secondary sulfonamides. These reactions occur at room temperature under visible light irradiation and are jointly catalyzed by an iridium(III) photocatalyst, a dialkyl phosphate base, and a thiol hydrogen atom donor. Reaction outcomes are consistent with the intermediacy of an N-centered sulfonamidyl radical generated via proton-coupled electron transfer activation of the sulfonamide N-H bond. Studies outlining the synthetic scope (>60 examples) and mechanistic features of the reaction are presented.

Photoredox-Catalyzed Intramolecular Aminodifluoromethylation of Unactivated Alkenes

Zhang, Zuxiao,Tang, Xiaojun,Thomoson, Charles S.,Dolbier, William R.

supporting information, p. 3528 - 3531 (2015/07/28)

A photoredox catalyzed aminodifluoromethylation of unactivated alkenes has been developed in which HCF2SO2Cl is used as the HCF2 radical source. Sulfonamides were active nucleophiles in the final step of a tandem addition/oxidation/cyclization process to form pyrrolidines, and esters were found to cyclize to form lactones. Thus, a variety of pyrrolidines and lactones were obtained in moderate to excellent yield. In order for the cyclization reactions to be efficient, a combination of a copper catalyst (Cu(dap)2Cl) and silver carbonate was crucial to suppressing a competing chloro, difluoroalkylation process.

Copper(II)-catalyzed enantioselective intramolecular carboamination of alkenes

Zeng, Wei,Chemler, Sherry R.

, p. 12948 - 12949 (2008/09/17)

The enantioselective oxidative cyclizations of γ-alkenyl arylsulfonamides and a δ-alkenyl arylsulfonamide for the synthesis of nitrogen heterocycles are presented. The reactions are catalyzed by chiral copper(II) complexes, and MnO2 is used as

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