Cas 1415753-04-6,2-((Z)-2((Z)-(4-nitrobenzylidene)hydrazinyl)-2-phenyvinyl)quinoline

1415753-04-6

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Basic information

Product Name: 2-((Z)-2((Z)-(4-nitrobenzylidene)hydrazinyl)-2-phenyvinyl)quinoline
Synonyms: 2-((Z)-2((Z)-(4-nitrobenzylidene)hydrazinyl)-2-phenyvinyl)quinoline
CAS NO:1415753-04-6
Molecular Formula:
Molecular Weight: 394.433
EINECS: N/A
Product Categories: N/A
Mol File: 1415753-04-6.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: 2-((Z)-2((Z)-(4-nitrobenzylidene)hydrazinyl)-2-phenyvinyl)quinoline(CAS DataBase Reference)
NIST Chemistry Reference: 2-((Z)-2((Z)-(4-nitrobenzylidene)hydrazinyl)-2-phenyvinyl)quinoline(1415753-04-6)
EPA Substance Registry System: 2-((Z)-2((Z)-(4-nitrobenzylidene)hydrazinyl)-2-phenyvinyl)quinoline(1415753-04-6)

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: 1415753-04-6(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1415753-04-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,1,5,7,5 and 3 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1415753-04:
(9*1)+(8*4)+(7*1)+(6*5)+(5*7)+(4*5)+(3*3)+(2*0)+(1*4)=146
146 % 10 = 6
So 1415753-04-6 is a valid CAS Registry Number.

1415753-04-6Upstream product

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1415753-04-6Relevant articles and documents

Tautomerism in 2-ketomethylquinolineazines

Loghmani-Khouzani, Hossein,Minaeifar, Alireza,Gawinecki, Ryszard

, p. 138 - 146 (2013/02/23)

A series of new azines were prepared in three steps. Structures of all compounds have been elucidated using spectroscopic methods and elemental analysis. Our studies show that in chloroform solution generally two tautomeric forms are in equilibrium. In some cases, one tautomer was the dominant species.

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