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5,7-dimethoxy-2,3-dihydro-1-[4,6-dimethoxy-3-phenylindol-2-yl]-1,3,3-trimethyl-4-phenyl-1H-pyrrolo[1,2-a]indole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1238398-72-5

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1238398-72-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1238398-72-5 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,3,8,3,9 and 8 respectively; the second part has 2 digits, 7 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1238398-72:
(9*1)+(8*2)+(7*3)+(6*8)+(5*3)+(4*9)+(3*8)+(2*7)+(1*2)=185
185 % 10 = 5
So 1238398-72-5 is a valid CAS Registry Number.

1238398-72-5Downstream Products

1238398-72-5Relevant academic research and scientific papers

Acid-catalyzed reactions of 3-substituted-4,6-dimethoxyindoles with ketones

Wood, Kasey,Black, David StC.,Kumar, Naresh

experimental part, p. 761 - 770 (2011/08/03)

Activated 3-substituted-4,6-dimethoxyindoles undergo acid catalyzed condensation with acetone and acetophenones in the presence of hydrochloric acid to give pyrrolo[a]indoles. Mixed pyrrolo[a]indoles can similarly be formed using a 1:1 mixture of two indo

Reactions of electron-rich indoles with triflic anhydride

Yepuri, Nageshwar R.,Haritakul, Rachada,Keller, Paul A.,Skelton, Brian W.,White, Allan H.

experimental part, p. 2501 - 2504 (2009/09/05)

The reaction of electron-rich 3-aryl-substituted 4,6-dimethoxyindoles in the presence of base with triflic anhydride results in biaryl coupling, producing both 2,2′- and 2,7′-biindoles. Further, if acetone is present, the corresponding vinyl triflate is f

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