Cas 1354628-17-3,5-(1-hydroxynaphthalen-2-yl)-1-methyl-3-phenyl-1H-imidazo[4,5-b]pyridine-2(3H)-thione

1354628-17-3

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Basic information

Product Name: 5-(1-hydroxynaphthalen-2-yl)-1-methyl-3-phenyl-1H-imidazo[4,5-b]pyridine-2(3H)-thione
Synonyms: 5-(1-hydroxynaphthalen-2-yl)-1-methyl-3-phenyl-1H-imidazo[4,5-b]pyridine-2(3H)-thione
CAS NO:1354628-17-3
Molecular Formula:
Molecular Weight: 383.473
EINECS: N/A
Product Categories: N/A
Mol File: 1354628-17-3.mol
Article Data: 1

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-(1-hydroxynaphthalen-2-yl)-1-methyl-3-phenyl-1H-imidazo[4,5-b]pyridine-2(3H)-thione(CAS DataBase Reference)
NIST Chemistry Reference: 5-(1-hydroxynaphthalen-2-yl)-1-methyl-3-phenyl-1H-imidazo[4,5-b]pyridine-2(3H)-thione(1354628-17-3)
EPA Substance Registry System: 5-(1-hydroxynaphthalen-2-yl)-1-methyl-3-phenyl-1H-imidazo[4,5-b]pyridine-2(3H)-thione(1354628-17-3)

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: 1354628-17-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1354628-17-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,4,6,2 and 8 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1354628-17:
(9*1)+(8*3)+(7*5)+(6*4)+(5*6)+(4*2)+(3*8)+(2*1)+(1*7)=163
163 % 10 = 3
So 1354628-17-3 is a valid CAS Registry Number.

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1354628-17-3Relevant articles and documents

2,3-Unsubstituted chromones and their enaminone precursors as versatile reagents for the synthesis of fused pyridines

Iaroshenko, Viktor O.,Mkrtchyan, Satenik,Gevorgyan, Ashot,Miliutina, Mariia,Villinger, Alexander,Volochnyuk, Dmytro,Sosnovskikh, Vyacheslav Ya.,Langer, Peter

supporting information; experimental part, p. 890 - 894 (2012/02/02)

A divergent and regioselective approach to fused pyridines was developed through formal [3 + 3] cyclocondensations from simple 2,3-unsubstituted chromones or their enaminone precursors.

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