Cas 161139-83-9,1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-2-(3'',5''-dimethoxyphenylamino)ethanone

161139-83-9

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Basic information

Product Name: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-2-(3'',5''-dimethoxyphenylamino)ethanone
Synonyms: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-2-(3'',5''-dimethoxyphenylamino)ethanone
CAS NO:161139-83-9
Molecular Formula:
Molecular Weight: 522.601
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-2-(3'',5''-dimethoxyphenylamino)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-2-(3'',5''-dimethoxyphenylamino)ethanone(161139-83-9)
EPA Substance Registry System: 1-(4',6'-dimethoxy-2',3'-diphenylindol-7'-yl)-2-(3'',5''-dimethoxyphenylamino)ethanone(161139-83-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 161139-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 161139-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,1,3 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 161139-83:
(8*1)+(7*6)+(6*1)+(5*1)+(4*3)+(3*9)+(2*8)+(1*3)=119
119 % 10 = 9
So 161139-83-9 is a valid CAS Registry Number.

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161139-83-9Relevant academic research and scientific papers

Synthesis of Activated 3-Arylindoles

Black, David St. C.,Bowyer, Michael C.,Bowyer, Paul K.,Ivory, Andrew J.,Kim, Mihyong,et al.

, p. 1741 - 1750 (2007/10/02)

A wide range of substituted 3-aryl-4,6-dimethoxyindoles (6) has been synthesized from the related α-anilinoacetophenones (5), in which the nitrogen atom is protected by a trifluoroacetyl or acetyl group.This method has led to the synthesis of a 3,7'-biindolyl (12).

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