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3-((2-methoxyphenyl)selenyl)-1H-indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1599461-85-4

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1599461-85-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1599461-85-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,9,9,4,6 and 1 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1599461-85:
(9*1)+(8*5)+(7*9)+(6*9)+(5*4)+(4*6)+(3*1)+(2*8)+(1*5)=234
234 % 10 = 4
So 1599461-85-4 is a valid CAS Registry Number.

1599461-85-4Downstream Products

1599461-85-4Relevant academic research and scientific papers

Direct, Metal-free C(sp2)?H Chalcogenation of Indoles and Imidazopyridines with Dichalcogenides Catalysed by KIO3

Rafique, Jamal,Saba, Sumbal,Franco, Marcelo S.,Bettanin, Luana,Schneider, Alex R.,Silva, Lais T.,Braga, Antonio L.

, p. 4173 - 4180 (2018)

Herein, we report a greener protocol for the synthesis of 3-Se/S-indoles and imidazo[1,2-a]pyridines through direct C(sp2)?H bond chalcogenation of heteroarenes with half molar equivalents of different dichalcogenides, using KIO3 as a non-toxic, easy-to-handle catalyst and a stoichiometric amount of glycerol. The reaction features are high yields, based on atom economy, easy performance on gram-scale, metal- and solvent-free conditions as well as applicability to different types of N-heteroarenes.

Rose Bengal catalysed photo-induced selenylation of indoles, imidazoles and arenes: A metal free approach

Saba, Sumbal,Rafique, Jamal,Franco, Marcelo S.,Schneider, Alex R.,Espíndola, Leandro,Silva, Dagoberto O.,Braga, Antonio L.

supporting information, p. 880 - 885 (2018/02/19)

In this report, the highly efficient Rose Bengal-catalysed C(sp2)-H selenylation of indoles, imidazoles and arenes was achieved using a half molar equiv. of diorganoyl diselenides. This metal-free, photo-induced protocol resulted in selenylated

Synthesis of 3-Selenylindoles under Ecofriendly Conditions

Ferreira, Natasha L.,Azeredo, Juliano B.,Fiorentin, Breno L.,Braga, Antonio L.

supporting information, p. 5070 - 5074 (2015/08/18)

The preparation of biologically relevant 3-selenylindoles by a greener protocol by using a catalytic amount of K2CO3 and ethanol as a biosolvent in a system open to air was explored. Through this easy approach, 3-selenylindoles with

A solvent- and metal-free synthesis of 3-chacogenyl-indoles employing DMSO/I2 as an eco-friendly catalytic oxidation system

Azeredo, Juliano B.,Godoi, Marcelo,Martins, Guilherme M.,Silveira, Claudio C.,Braga, Antonio L.

, p. 4125 - 4130 (2014/05/20)

Herein, we describe a solvent- and metal-free method for the synthesis of 3-chalcogenyl-indoles from indoles and diorganyl dichalcogenides using an equivalent amount of DMSO as an oxidant, under catalysis by molecular iodine. This mild and eco-friendly ap

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