Cas 1327166-90-4,2-bromo-9,10-dihydro-6-p-tolyl-7-azaindolizino[1,2-c]quinolin-12(8H)-one

1327166-90-4

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Basic information

Product Name: 2-bromo-9,10-dihydro-6-p-tolyl-7-azaindolizino[1,2-c]quinolin-12(8H)-one
Synonyms: 2-bromo-9,10-dihydro-6-p-tolyl-7-azaindolizino[1,2-c]quinolin-12(8H)-one
CAS NO:1327166-90-4
Molecular Formula:
Molecular Weight: 406.282
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: 2-bromo-9,10-dihydro-6-p-tolyl-7-azaindolizino[1,2-c]quinolin-12(8H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 2-bromo-9,10-dihydro-6-p-tolyl-7-azaindolizino[1,2-c]quinolin-12(8H)-one(1327166-90-4)
EPA Substance Registry System: 2-bromo-9,10-dihydro-6-p-tolyl-7-azaindolizino[1,2-c]quinolin-12(8H)-one(1327166-90-4)

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: 1327166-90-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1327166-90-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,2,7,1,6 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1327166-90:
(9*1)+(8*3)+(7*2)+(6*7)+(5*1)+(4*6)+(3*6)+(2*9)+(1*0)=154
154 % 10 = 4
So 1327166-90-4 is a valid CAS Registry Number.

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1327166-90-4Relevant academic research and scientific papers

Cascade reaction of isatins with heterocyclic ketene aminals: Synthesis of imidazopyrroloquinoline derivatives

Yu, Fuchao,Yan, Shengjiao,Hu, Ling,Wang, Yongchao,Lin, Jun

supporting information; experimental part, p. 4782 - 4785 (2011/11/12)

A concise and efficient route for the synthesis of highly substituted imidazopyrroloquinoline derivatives by simply refluxing a reaction mixture of different types of isatins and heterocyclic ketene aminals (HKAs) by acetic acid was developed. This method

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