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1-(2-(2-bromophenethyl)-1H-indol-1-yl)ethanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1403485-72-2

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1403485-72-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1403485-72-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,3,4,8 and 5 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1403485-72:
(9*1)+(8*4)+(7*0)+(6*3)+(5*4)+(4*8)+(3*5)+(2*7)+(1*2)=142
142 % 10 = 2
So 1403485-72-2 is a valid CAS Registry Number.

1403485-72-2Downstream Products

1403485-72-2Relevant academic research and scientific papers

Ir(I)-catalyzed C-H bond alkylation of C2-position of indole with alkenes: Selective synthesis of linear or branched 2-alkylindoles

Pan, Shiguang,Ryu, Naoto,Shibata, Takanori

, p. 17474 - 17477,4 (2012/12/12)

A cationic iridium-catalyzed C2-alkylation of N-substituted indole derivatives with various alkenes has been developed, which selectively gives linear or branched 2-alkylindoles in high to excellent selectivity. This protocol relies on the use of the carbonyl group on the nitrogen atom of indole as a directing group: a linear product was predominant when an acetyl group was used as a directing group, and a branched product was predominant with a benzoyl group.

Ir(I)-catalyzed C-H bond alkylation of C2-position of indole with alkenes: Selective synthesis of linear or branched 2-alkylindoles

Pan, Shiguang,Ryu, Naoto,Shibata, Takanori

, p. 17474 - 17477 (2013/01/15)

A cationic iridium-catalyzed C2-alkylation of N-substituted indole derivatives with various alkenes has been developed, which selectively gives linear or branched 2-alkylindoles in high to excellent selectivity. This protocol relies on the use of the carbonyl group on the nitrogen atom of indole as a directing group: a linear product was predominant when an acetyl group was used as a directing group, and a branched product was predominant with a benzoyl group.

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