Cas 1401073-66-2,(E)-methyl 3-(3-(2-oxo-2-p-tolyl-1-(m-tolylamino)ethyl)-1H-indol-5-yl)acrylate

1401073-66-2

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Basic information

Product Name: (E)-methyl 3-(3-(2-oxo-2-p-tolyl-1-(m-tolylamino)ethyl)-1H-indol-5-yl)acrylate
Synonyms: (E)-methyl 3-(3-(2-oxo-2-p-tolyl-1-(m-tolylamino)ethyl)-1H-indol-5-yl)acrylate
CAS NO:1401073-66-2
Molecular Formula:
Molecular Weight: 438.526
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: (E)-methyl 3-(3-(2-oxo-2-p-tolyl-1-(m-tolylamino)ethyl)-1H-indol-5-yl)acrylate(CAS DataBase Reference)
NIST Chemistry Reference: (E)-methyl 3-(3-(2-oxo-2-p-tolyl-1-(m-tolylamino)ethyl)-1H-indol-5-yl)acrylate(1401073-66-2)
EPA Substance Registry System: (E)-methyl 3-(3-(2-oxo-2-p-tolyl-1-(m-tolylamino)ethyl)-1H-indol-5-yl)acrylate(1401073-66-2)

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: 1401073-66-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1401073-66-2 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, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1401073-66:
(9*1)+(8*4)+(7*0)+(6*1)+(5*0)+(4*7)+(3*3)+(2*6)+(1*6)=102
102 % 10 = 2
So 1401073-66-2 is a valid CAS Registry Number.

1401073-66-2Upstream product

111168-53-7 methyl 3-(1H-indol-5-yl)acrylate

1401073-66-2Downstream Products

1401073-66-2Relevant 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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