Cas 1194451-28-9,(E)-3-(2-(4-methoxyphenyl)-5,6-dihydro-4H-benzo[kl]acridin-3-yl)-3-(piperidin-1-yl)acrylonitrile

1194451-28-9

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Basic information

Product Name: (E)-3-(2-(4-methoxyphenyl)-5,6-dihydro-4H-benzo[kl]acridin-3-yl)-3-(piperidin-1-yl)acrylonitrile
Synonyms: (E)-3-(2-(4-methoxyphenyl)-5,6-dihydro-4H-benzo[kl]acridin-3-yl)-3-(piperidin-1-yl)acrylonitrile
CAS NO:1194451-28-9
Molecular Formula:
Molecular Weight: 459.591
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)-3-(2-(4-methoxyphenyl)-5,6-dihydro-4H-benzo[kl]acridin-3-yl)-3-(piperidin-1-yl)acrylonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (E)-3-(2-(4-methoxyphenyl)-5,6-dihydro-4H-benzo[kl]acridin-3-yl)-3-(piperidin-1-yl)acrylonitrile(1194451-28-9)
EPA Substance Registry System: (E)-3-(2-(4-methoxyphenyl)-5,6-dihydro-4H-benzo[kl]acridin-3-yl)-3-(piperidin-1-yl)acrylonitrile(1194451-28-9)

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: 1194451-28-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1194451-28-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,9,4,4,5 and 1 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1194451-28:
(9*1)+(8*1)+(7*9)+(6*4)+(5*4)+(4*5)+(3*1)+(2*2)+(1*8)=159
159 % 10 = 9
So 1194451-28-9 is a valid CAS Registry Number.

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1194451-28-9Relevant academic research and scientific papers

Unprecedented bridged annulation approach to the construction of 5,6-Dihydro-4H-benzo[k/]acridines

Goel, Atul,Singh, Salil Pratap,Kumar, Amit,Kant, Ruchir,Maulik, Prakas R.

supporting information; experimental part, p. 5122 - 5125 (2009/12/28)

A general and novel "bridged annulation" methodology for the synthesis of 5,6-dihydro-4H-benzo[k/|acridines has been developed via Michael addition of a conjugate base of 9-methyl-3,4-dihydroacridin-1(2H)-one to various cyclic or acyclic α,β-unsaturated c

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