Cas 369654-41-1,6-hydroxy-2-oxo-4-phenyl-5-(phenyldiazenyl)-1,2-dihydropyridine-3-carbonitrile

369654-41-1

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Basic information

Product Name: 6-hydroxy-2-oxo-4-phenyl-5-(phenyldiazenyl)-1,2-dihydropyridine-3-carbonitrile
Synonyms: 6-hydroxy-2-oxo-4-phenyl-5-(phenyldiazenyl)-1,2-dihydropyridine-3-carbonitrile
CAS NO:369654-41-1
Molecular Formula:
Molecular Weight: 316.319
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: 6-hydroxy-2-oxo-4-phenyl-5-(phenyldiazenyl)-1,2-dihydropyridine-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 6-hydroxy-2-oxo-4-phenyl-5-(phenyldiazenyl)-1,2-dihydropyridine-3-carbonitrile(369654-41-1)
EPA Substance Registry System: 6-hydroxy-2-oxo-4-phenyl-5-(phenyldiazenyl)-1,2-dihydropyridine-3-carbonitrile(369654-41-1)

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: 369654-41-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 369654-41-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,9,6,5 and 4 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 369654-41:
(8*3)+(7*6)+(6*9)+(5*6)+(4*5)+(3*4)+(2*4)+(1*1)=191
191 % 10 = 1
So 369654-41-1 is a valid CAS Registry Number.

369654-41-1Upstream product

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369654-41-1Relevant academic research and scientific papers

The microwave-assisted synthesis of 5-arylazo-4,6-disubstituted-3-cyano-2-pyridone dyes

Mijin, Du?an Z.,Baghbanzadeh, Mostafa,Reidlinger, Claudia,Oliver Kappe

experimental part, p. 73 - 78 (2010/10/21)

A novel protocol for the rapid synthesis of pyridone colorants under controlled microwave irradiation in a dedicated reactor is described. Short reaction times, high isolated yields, and versatility for different substrates are the advantages of the reported method.

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