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906770-99-8

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906770-99-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 906770-99-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,6,7,7 and 0 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 906770-99:
(8*9)+(7*0)+(6*6)+(5*7)+(4*7)+(3*0)+(2*9)+(1*9)=198
198 % 10 = 8
So 906770-99-8 is a valid CAS Registry Number.

906770-99-8Downstream Products

906770-99-8Relevant academic research and scientific papers

Synthesis of Substituted Anilines from Cyclohexanones Using Pd/C-Ethylene System and Its Application to Indole Synthesis

Maeda, Katsumi,Matsubara, Ryosuke,Hayashi, Masahiko

supporting information, p. 1530 - 1534 (2021/03/08)

The synthesis of anilines and indoles from cyclohexanones using a Pd/C-ethylene system is reported. A simple combination of NH4OAc and K2CO3 under nonaerobic conditions was found to be the most suitable to perform this reaction. Hydrogen transfer between cyclohexanone and ethylene generates the desired products. The reaction tolerates a variety of substitutions on the starting cyclohexanones.

Modular counter-Fischer?indole synthesis through radical-enolate coupling

Chung, Hyunho,Kim, Jeongyun,Gonzalez-Montiel, Gisela A.,Cheong, Paul Ha-Yeon,Lee, Hong Geun

, p. 1096 - 1102 (2021/01/26)

A single-electron transfer mediated modular indole formation reaction from a 2-iodoaniline derivative and a ketone has been developed. This transition-metal-free reaction shows a broad substrate scope and unconventional regioselectivity trends. Moreover, important functional groups for further transformation are tolerated under the reaction conditions. Density functional theory studies reveal that the reaction proceeds by metal coordination, which converts a disfavored 5-endo-trig cyclization to an accessible 7-endo-trig process.

[Cp?IrCl2]2-catalysed cyclization of 2-alkynylanilines into indoles

Kumaran, Elumalai,Leong, Weng Kee

supporting information, p. 5495 - 5498 (2014/12/11)

[Cp?IrCl2]2 catalyses the cyclization of 2-alkynylanilines into indoles. A wide variety of substrates is tolerated. A reaction pathway involving intramolecular hydroamination is proposed.

Heterobimetallic cobalt/rhodium nanoparticle-catalyzed carbonylative cycloaddition of 2-alkynylanilines to oxindoles

Park, Ji Hoon,Kim, Eunha,Chung, Young Keun

supporting information; experimental part, p. 4718 - 4721 (2009/05/31)

(Chemical Equation Presented) The cobalt-rhodium heterobimetallic nanoparticle-catalyzed synthesis of oxindoles from 2-alkynylanilines in the presence of carbon monoxide is described.

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