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7-(indol-2'-yl)-4,6-dimethoxy-2,3-diphenylindole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

91107-13-0

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91107-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 91107-13-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,1,1,0 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 91107-13:
(7*9)+(6*1)+(5*1)+(4*0)+(3*7)+(2*1)+(1*3)=100
100 % 10 = 0
So 91107-13-0 is a valid CAS Registry Number.

91107-13-0Downstream Products

91107-13-0Relevant academic research and scientific papers

Synthesis of biindolyls by the reaction of indoles with indolin-2-ones and phosphoryl chloride or trifluoromethanesulfonic anhydride

Black, David StC.,Ivory, Andrew J.,Kumar, Naresh

, p. 4697 - 4708 (2007/10/03)

Examples of 2,2'-,2,3'- and 2,7'-biindolyls have been prepared by the reaction of indoles with indolin-2-ones and phosphoryl chloride or trifluoromethanesulfonic anhydride. In certain conditions terindolyls can also be formed and those described contained combinations of the above linkages.

Reactivity of 3-substituted indolin-2-ones in Vilsmeier-type reactions of 4,6-dimethoxyindoles

Black, David St.C.,Ivory, Andrew J.,Kumar, Naresh

, p. 7003 - 7012 (2007/10/03)

4,6-Dimethoxy-2,3-diphenylindole 1 undergoes reaction with the 3-substituted indolin-2-ones 7,8,11-14 and either phosphoryl chloride or triflic anhydride to give the 2,7'-biindolyl 16, the 7,7'; 2,7'-terindolyls 19, 20 and the 7,7'-biindolyl 23.

A General Strategy for the Synthesis of 2,2'-, 2,3'-, and 2,7'-Bi-indolyls

Black, David St. C.,Kumar, Naresh

, p. 441 - 442 (2007/10/02)

Various substituted indoles undergo electrophilic substitution with indolin-2-one or 4,6-dimethoxyindolin-2-one and phosphoryl chloride to afford 2,2'-, 2,3'-, or 2,7'-bi-indolyls, depending on the initial substitution pattern.

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