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2-(4-bromophenyl)-1-(4-chlorophenyl)-6,7-dihydro-6,6-dimethyl-3-(2-phenyl-1H-indol-3-yl)-1H-indol-4(5H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1421844-90-7

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1421844-90-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1421844-90-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,1,8,4 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1421844-90:
(9*1)+(8*4)+(7*2)+(6*1)+(5*8)+(4*4)+(3*4)+(2*9)+(1*0)=147
147 % 10 = 7
So 1421844-90-7 is a valid CAS Registry Number.

1421844-90-7Downstream Products

1421844-90-7Relevant academic research and scientific papers

Efficient synthesis of 3,3′-bisindoles catalyzed by Fe3O4@MCM-48-OSO3H magnetic core-shell nanoparticles

Khorshidi, Alireza,Shariati, Shahab

, p. 778 - 784 (2015)

Magnetite nanoparticles coated with sulfuric acid-functionalized mesoporous MCM-48 were synthesized and used as a catalyst in three-component domino reactions of indoles, arylglyoxal monohydrates and N-arylenaminones to furnish the desired 3,3′-bisindoles by formation of two C-C and one C-N bonds in a smooth cascade with good yields under mild reaction conditions. The catalyst was recovered easily and maintained activity in successive runs.

Three-component domino reactions for regioselective formation of bis-indole derivatives

Fu, Li-Ping,Shi, Qing-Qing,Shi, Yu,Jiang, Bo,Tu, Shu-Jiang

supporting information, p. 135 - 140 (2013/03/14)

A microwave-assisted regioselective reaction dealing with arylglyoxal monohydrate, diverse N-aryl enaminones, and indoles to achieve 3,2′- and 3,3′-bis-indoles by varying a substituted indole substrate is reported. The 2-unsubstituted indoles resulted in the 3,2′-bis-indole skeleton, whereas indoles bearing a methyl or phenyl group at C2 led to the 3,3′-bis-indoles with simultaneous formation of three sigma-bonds. The procedures feature excellent regioselectivity, short reaction times, convenient one-pot manner, and operational simplicity.

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