Cas 1417895-16-9,5-(furan-2-yl)-3-(4-methoxybenzyl)-2-p-tolyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine

1417895-16-9

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Basic information

Product Name: 5-(furan-2-yl)-3-(4-methoxybenzyl)-2-p-tolyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine
Synonyms: 5-(furan-2-yl)-3-(4-methoxybenzyl)-2-p-tolyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine
CAS NO:1417895-16-9
Molecular Formula:
Molecular Weight: 463.459
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: 5-(furan-2-yl)-3-(4-methoxybenzyl)-2-p-tolyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine(CAS DataBase Reference)
NIST Chemistry Reference: 5-(furan-2-yl)-3-(4-methoxybenzyl)-2-p-tolyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine(1417895-16-9)
EPA Substance Registry System: 5-(furan-2-yl)-3-(4-methoxybenzyl)-2-p-tolyl-7-(trifluoromethyl)-3H-imidazo[4,5-b]pyridine(1417895-16-9)

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: 1417895-16-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1417895-16-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,7,8,9 and 5 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1417895-16:
(9*1)+(8*4)+(7*1)+(6*7)+(5*8)+(4*9)+(3*5)+(2*1)+(1*6)=189
189 % 10 = 9
So 1417895-16-9 is a valid CAS Registry Number.

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1417895-16-9Relevant academic research and scientific papers

Transition-metal-catalyzed arylation of 1-deazapurines via C-H bond activation

Iaroshenko, Viktor O.,Ali, Iftikhar,Mkrtchyan, Satenik,Semeniuchenko, Volodymyr,Ostrovskyi, Dmytro,Langer, Peter

supporting information, p. 2603 - 2608 (2013/01/15)

Transition-metal-catalyzed arylation of imidazo[4,5-b]pyridines (known as 1-deazapurines) is reported. 1-Deazapurines were synthesized from 5-aminoimidazoles, generated in situ by the reaction of methyl N-(cyanomethyl)formimidate with primary amines. Geor

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