Cas 1427284-19-2,2-(4-methoxyphenyl)-6,6-dimethyl-3-((4-nitrophenyl)amino)-1-phenyl-6,7-dihydro-1H-indol-4(5H)-one

1427284-19-2

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Basic information

Product Name: 2-(4-methoxyphenyl)-6,6-dimethyl-3-((4-nitrophenyl)amino)-1-phenyl-6,7-dihydro-1H-indol-4(5H)-one
Synonyms: 2-(4-methoxyphenyl)-6,6-dimethyl-3-((4-nitrophenyl)amino)-1-phenyl-6,7-dihydro-1H-indol-4(5H)-one
CAS NO:1427284-19-2
Molecular Formula:
Molecular Weight: 481.551
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: 2-(4-methoxyphenyl)-6,6-dimethyl-3-((4-nitrophenyl)amino)-1-phenyl-6,7-dihydro-1H-indol-4(5H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-(4-methoxyphenyl)-6,6-dimethyl-3-((4-nitrophenyl)amino)-1-phenyl-6,7-dihydro-1H-indol-4(5H)-one(1427284-19-2)
EPA Substance Registry System: 2-(4-methoxyphenyl)-6,6-dimethyl-3-((4-nitrophenyl)amino)-1-phenyl-6,7-dihydro-1H-indol-4(5H)-one(1427284-19-2)

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: 1427284-19-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1427284-19-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,2,7,2,8 and 4 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 1427284-19:
(9*1)+(8*4)+(7*2)+(6*7)+(5*2)+(4*8)+(3*4)+(2*1)+(1*9)=162
162 % 10 = 2
So 1427284-19-2 is a valid CAS Registry Number.

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1427284-19-2Relevant academic research and scientific papers

Multicomponent formation of fused pyrroles through p-TsOH promoted N-arylation

Li, Ying,Li, Qiu-Yun,Xu, Hai-Wei,Fan, Wei,Jiang, Bo,Wang, Shu-Liang,Tu, Shu-Jiang

supporting information, p. 2941 - 2946 (2013/04/10)

Concise and efficient N-arylation-based domino [3+2] heterocyclization promoted by p-TsOH has been established for the synthesis of 27 examples of 3-arylamino substituted fused pyrrole derivatives in 70-90% yields. The present methodology shows attractive

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