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1-methyl-1-(2-methyl-1H-3-indolyl)ethyl (4-methylphenyl)sulfone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

911303-07-6

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911303-07-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 911303-07-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,1,3,0 and 3 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 911303-07:
(8*9)+(7*1)+(6*1)+(5*3)+(4*0)+(3*3)+(2*0)+(1*7)=116
116 % 10 = 6
So 911303-07-6 is a valid CAS Registry Number.

911303-07-6Relevant academic research and scientific papers

Catalyst-free synthesis of 3-(1-arylsulfonylalkyl)indoles via three-component reaction of indoles, carbonyls, and arenesulfinic acids

Huang, Wenzhong,Yang, Juan,Li, Xiangguang,Yuan, Lin,Ma, Yinhai,Zhou, Qinglong,Liang, Deqiang

supporting information, p. 772 - 777 (2016/05/09)

A catalyst-free three-component reaction of indoles, carbonyls, and arenesulfinic acids performed at room temperature provides direct access to biologically important 3-(1-arylsulfonylalkyl)indoles. This process features mild conditions, low cost, broad s

Highly enantioselective monofluoromethylation of C2-arylindoles using FBSM under chiral phase-transfer catalysis

Matsuzaki, Kohei,Furukawa, Tatsuya,Tokunaga, Etsuko,Matsumoto, Takashi,Shiro, Motoo,Shibata, Norio

, p. 3282 - 3285 (2013/07/26)

The highly enantioselective addition of 1-fluoro-1,1-bis(phenylsulfonyl) methane (FBSM) to vinylogous imines generated in situ from 2-aryl-3-(1- arylsulfonylmethyl)indoles was achieved using chiral ammonium salts derived from cinchona alkaloids. One-pot c

Highly enantioselective michael addition of malononitrile to vinylogous imine intermediates generated in situ from arylsulfonyl indoles

Jing, Linhai,Wei, Jiangtao,Zhou, Li,Huang, Zhiyong,Li, Zhengkai,Wu, Di,Xiang, Haifeng,Zhou, Xiangge

supporting information; experimental part, p. 10955 - 10958 (2010/11/05)

(Figure Presented) Malononitrile on rare form: Highly enantioselective Michael addition of malononitrile to vinylogous imine intermediates 2, generated in situ from arylsulfonyl indoles 1, is described (see scheme). This protocol provides easy and conveni

Amberlyst-15: an efficient and reusable catalyst for the Friedel-Crafts reactions of activated arenes and heteroarenes with α-amido sulfones

Kadam, Santosh T.,Thirupathi, Ponnaboina,Kim, Sung Soo

experimental part, p. 10383 - 10389 (2010/02/27)

The heterogeneous Amberlyst-15 catalyst displays efficient catalytic properties for the Friedel-Crafts reactions between an activated arenes or heteroarenes and α-amido sulfones. Various α-amido sulfones on treatment with 1,2,4-trimethoxy benzene give the

InBr3: A versatile catalyst for the different types of Friedel-Crafts reactions

Thirupathi, Ponnaboina,Sung, Soo Kim

scheme or table, p. 7755 - 7761 (2009/12/27)

(Chemical Equation Presented) Mild and efficient InBr3-catalyzed Friedel-Crafts alkylation of heteroaromatic or electron-rich aromatic compounds with α-amido sulfones at room temperature in CH2Cl2 has been developed. The p

Simplified synthesis of 3-(1-arylsulfonylalkyl) indoles and their reaction with reformatsky reagents

Palmieri, Alessandro,Petrini, Marino

, p. 1863 - 1866 (2007/10/03)

A simple procedure for the preparation of 3-(1-arylsulfonylalkyl) indoles by three-component condensation of indoles, carbonyls, and arenesulfinic acids is presented. The obtained products undergo a Reformatsky reaction leading to alkyl 3-(3-indolyl) alka

Solventless clay-promoted Friedel-Crafts reaction of indoles with α-amido sulfones: Unexpected synthesis of 3-(1-arylsulfonylalkyl) indoles

Ballini, Roberte,Palmieri, Alessandro,Petrini, Marino,Torregiani, Elisabetta

, p. 4093 - 4096 (2007/10/03)

Friedel-Crafts reaction of indoles with α-amido sulfones in the presence of montmorillonite K-10 leads unexpectedly to 3-(1-arylsulfonylalkyl) indoles in good yield. The obtained products can be further desulfonylated under reductive or alkylative conditi

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