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1-(1-((4-chlorophenyl)sulfonyl)-1H-indol-3-yl)ethan-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

104142-23-6

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104142-23-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 104142-23-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,4,1,4 and 2 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 104142-23:
(8*1)+(7*0)+(6*4)+(5*1)+(4*4)+(3*2)+(2*2)+(1*3)=66
66 % 10 = 6
So 104142-23-6 is a valid CAS Registry Number.

104142-23-6Relevant academic research and scientific papers

Access to biaryl sulfonamides by palladium-catalyzed intramolecular oxidative coupling and subsequent nucleophilic ring opening of heterobiaryl sultams with amines

Laha, Joydev K.,Dayal, Neetu,Jethava, Krupal P.,Prajapati, Dilip V.

, p. 1296 - 1299 (2015)

The installation of sulfonamide pharmacophores on heterobiaryls has successfully been executed by a previously unknown palladium-catalyzed intramolecular oxidative coupling in N-arylsulfonyl heterocycles followed by novel ring opening of heterobiaryl sultams with amine nucleophiles. The protocol has a wide scope of substrates warranting broad applications in the synthesis of heterobiaryls containing an o-sulfonyl or carboxyl functional group.

Synthesis and bioactivity assessment of novel spiro pyrazole-oxindole congeners exhibiting potent and selective in vitro anticancer effects

Abdelhamid, Sayeda A.,Abo-Salem, Heba M.,Aboul-Soud, Mourad A. M.,Al-Sheikh, Yazeed A.,Ebied, Manal S.,El-Sawy, Eslam R.,Elawady, Mohamed E.,Nassrallah, Amr,Soliman, Ahmed A. F.

, (2020)

The present work aims to design and synthesize novel series of spiro pyrazole-3,3'-oxindoles analogues and investigate their bioactivity as antioxidant and antimicrobial agents, as well as antiproliferative potency against selected human cancerous cell li

Synthesis and quantitative structure-activity relationship (QSAR) study of novel N-arylsulfonyl-3-acylindole arylcarbonyl hydrazone derivatives as nematicidal agents

Che, Zhiping,Zhang, Shaoyong,Shao, Yonghua,Fan, Lingling,Xu, Hui,Yu, Xiang,Zhi, Xiaoyan,Yao, Xiaojun,Zhang, Rui

, p. 5696 - 5705 (2013/07/26)

In continuation of our program aimed at the discovery and development of natural-product-based pesticidal agents, 54 novel N-arylsulfonyl-3-acylindole arylcarbonyl hydrazone derivatives were prepared, and their structures were well characterized by 1

Anti HIV-1 agents 5: Synthesis and anti-HIV-1 activity of some N-arylsulfonyl-3-acetylindoles in vitro

Ran, Jun-Qiang,Huang, Ning,Xu, Hui,Yang, Liu-Meng,Lv, Min,Zheng, Yong-Tang

supporting information; experimental part, p. 3534 - 3536 (2010/08/21)

In continuation of our program aimed at the discovery and development of compounds with superior anti-human immunodeficiency virus type 1 (HIV-1) activity, 21N-arylsulfonyl-3-acetylindole analogs (2a-u) were synthesized and preliminarily evaluated as HIV-

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