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3-methyl-1-phenyl-3-((phenylsulfonyl)methyl)indolin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1588429-89-3

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1588429-89-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1588429-89-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,8,8,4,2 and 9 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1588429-89:
(9*1)+(8*5)+(7*8)+(6*8)+(5*4)+(4*2)+(3*9)+(2*8)+(1*9)=233
233 % 10 = 3
So 1588429-89-3 is a valid CAS Registry Number.

1588429-89-3Downstream Products

1588429-89-3Relevant academic research and scientific papers

Iron-catalyzed aerobic difunctionalization of alkenes: A highly efficient approach to construct oxindoles by C-S and C-C bond formation

Shen, Tao,Yuan, Yizhi,Song, Song,Jiao, Ning

, p. 4115 - 4118 (2014/04/03)

A novel iron-catalyzed efficient approach to construct sulfone-containing oxindoles, which play important roles in the structural library design and drug discovery, has been developed. The use of readily available benzenesulfinic acids, an inexpensive iron salt as the catalyst, and air as the oxidant makes this sulfur incorporation protocol very efficient and practical. This journal is the Partner Organisations 2014.

Catalyst-free direct arylsulfonylation of N-arylacrylamides with sulfinic acids: A convenient and efficient route to sulfonated oxindoles

Wei, Wei,Wen, Jiangwei,Yang, Daoshan,Du, Juan,You, Jinmao,Wang, Hua

supporting information, p. 2988 - 2991 (2014/06/10)

A simple, efficient and catalyst-free procedure has been developed for the construction of sulfonated oxindoles via the direct arylsulfonylation of N-arylacrylamides with sulfinic acids. The present protocol, which simply utilizes cheap oxidants, readily-available starting materials, and catalyst-free conditions, provides an alternative and highly attractive approach to a series of sulfonated oxindoles with high atom efficiency and excellent functional group tolerance. This journal is the Partner Organisations 2014.

Synthesis of oxindoles through silver-catalyzed trifluoromethylation-, difluoromethylation- and arylsulfonylation-cyclization reaction of N-arylacrylamides

Liu, Jidan,Zhuang, Shaobo,Gui, Qingwen,Chen, Xiang,Yang, Zhiyong,Tan, Ze

supporting information, p. 3196 - 3202 (2014/06/09)

Efficient synthesis of trifluoromethyl and difluoromethyl-substituted oxindoles was achieved by reacting Langlois reagent or Baran reagent with N-arylacrylamides. However, the reaction of aryl sulfinic acid sodium salts with N-arylacrylamides did not give the desulfinative products, instead, aryl sulfonated products were produced. Copyright

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