Cas 1401073-71-9,1-p-tolyl-2-(2-p-tolyl-1H-indol-3-yl)-2-(m-tolylamino)ethanone

1401073-71-9

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Basic information

Product Name: 1-p-tolyl-2-(2-p-tolyl-1H-indol-3-yl)-2-(m-tolylamino)ethanone
Synonyms: 1-p-tolyl-2-(2-p-tolyl-1H-indol-3-yl)-2-(m-tolylamino)ethanone
CAS NO:1401073-71-9
Molecular Formula:
Molecular Weight: 444.576
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-p-tolyl-2-(2-p-tolyl-1H-indol-3-yl)-2-(m-tolylamino)ethanone(CAS DataBase Reference)
NIST Chemistry Reference: 1-p-tolyl-2-(2-p-tolyl-1H-indol-3-yl)-2-(m-tolylamino)ethanone(1401073-71-9)
EPA Substance Registry System: 1-p-tolyl-2-(2-p-tolyl-1H-indol-3-yl)-2-(m-tolylamino)ethanone(1401073-71-9)

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: 1401073-71-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1401073-71-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,1,0,7 and 3 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1401073-71:
(9*1)+(8*4)+(7*0)+(6*1)+(5*0)+(4*7)+(3*3)+(2*7)+(1*1)=99
99 % 10 = 9
So 1401073-71-9 is a valid CAS Registry Number.

1401073-71-9Upstream product

55577-25-8 2-(4-methylphenyl)-1H-indole

1401073-71-9Downstream Products

1401073-71-9Relevant academic research and scientific papers

Direct α-arylation of α-amino carbonyl compounds with indoles using visible light photoredox catalysis

Wang, Zhi-Qiang,Hu, Ming,Huang, Xiao-Cheng,Gong, Lu-Bing,Xie, Ye-Xiang,Li, Jin-Heng

, p. 8705 - 8711 (2012/11/07)

A general and mild method for the construction of functionalized 2-(1H-indol-3-yl)-2-amino-carbonyl compounds was achieved, which represents the first example of direct α-arylation of α-amino carbonyl compounds with indoles using the visible light photoredox catalysis strategy.

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