Cas 1189176-76-8,12-(3,4-dimethylphenyl)-7,8,9,10,11,12-hexahydrobenzo[f]pyrimido[4,5-b]quinoline-9,11-dione

1189176-76-8

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Basic information

Product Name: 12-(3,4-dimethylphenyl)-7,8,9,10,11,12-hexahydrobenzo[f]pyrimido[4,5-b]quinoline-9,11-dione
Synonyms: 12-(3,4-dimethylphenyl)-7,8,9,10,11,12-hexahydrobenzo[f]pyrimido[4,5-b]quinoline-9,11-dione
CAS NO:1189176-76-8
Molecular Formula:
Molecular Weight: 369.423
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: 12-(3,4-dimethylphenyl)-7,8,9,10,11,12-hexahydrobenzo[f]pyrimido[4,5-b]quinoline-9,11-dione(CAS DataBase Reference)
NIST Chemistry Reference: 12-(3,4-dimethylphenyl)-7,8,9,10,11,12-hexahydrobenzo[f]pyrimido[4,5-b]quinoline-9,11-dione(1189176-76-8)
EPA Substance Registry System: 12-(3,4-dimethylphenyl)-7,8,9,10,11,12-hexahydrobenzo[f]pyrimido[4,5-b]quinoline-9,11-dione(1189176-76-8)

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: 1189176-76-8(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1189176-76-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,8,9,1,7 and 6 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1189176-76:
(9*1)+(8*1)+(7*8)+(6*9)+(5*1)+(4*7)+(3*6)+(2*7)+(1*6)=198
198 % 10 = 8
So 1189176-76-8 is a valid CAS Registry Number.

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1189176-76-8Relevant academic research and scientific papers

Green Method for the Synthesis of Benzo[f]pyrimido[4,5-b]quinoline Derivatives Catalyzed by Iodine in Aqueous Media

Wang, Xiang-Shan,Li, Qing,Wu, Jian-Rong,Zhang, Mei-Mei

, p. 3069 - 3080 (2009)

A convenient one-pot synthesis of benzo[f]pyrimido[4,5-b]quinoline derivatives is described via three-component reaction of benzaldehydes, naphthalen-2-amine, and barbituric acid at room temperature in aqueous media catalyzed by iodine. Compared with othe

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