Cas 7547-92-4,6H-pyrido[1,2-b]isoquinolin-6-one

7547-92-4

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Basic information

Product Name: 6H-pyrido[1,2-b]isoquinolin-6-one
Synonyms: benzo[b]quinolizin-6-one
CAS NO:7547-92-4
Molecular Formula: C₁₃H₉NO
Molecular Weight: 195.2167
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: 433.2°C at 760 mmHg
Flash Point: 219.6°C
Appearance: N/A
Density: 1.29g/cm³
Vapor Pressure: 1.05E-07mmHg at 25°C
Refractive Index: 1.705
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 6H-pyrido[1,2-b]isoquinolin-6-one(CAS DataBase Reference)
NIST Chemistry Reference: 6H-pyrido[1,2-b]isoquinolin-6-one(7547-92-4)
EPA Substance Registry System: 6H-pyrido[1,2-b]isoquinolin-6-one(7547-92-4)

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: 7547-92-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 7547-92-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,5,4 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7547-92:
(6*7)+(5*5)+(4*4)+(3*7)+(2*9)+(1*2)=124
124 % 10 = 4
So 7547-92-4 is a valid CAS Registry Number.

7547-92-4Upstream product

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7547-92-4Relevant academic research and scientific papers

Synthesis of aryl(di)azinyl ketones through copper- and iron-catalyzed oxidation of the methylene group of aryl(di)azinylmethanes

De Houwer, Johan,Abbaspour Tehrani, Kourosch,Maes, Bert U. W.

supporting information; experimental part, p. 2745 - 2748 (2012/04/10)

Sustainable Oxidations: An oxidation method to transform aryl(di)azinylmethanes into aryl(di)azinyl ketones is described. Base metals (copper and iron) as catalysts in combination with O2 as the oxidant are used, which makes this method sustainable. The utility of this method is illustrated by the synthesis of 6-(4-methylbenzoyl)pyridine-2-carbaldehyde, which is an intermediate in the preparation of the drug Acrivastine. Copyright

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