Cas 1206830-57-0,2-(5,7-diphenyl-1,2,3,4,4a,5-hexahydro-10H-benzimidazo[2,1-j]quinolin-10-ylidene)malonamide

1206830-57-0

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Basic information

Product Name: 2-(5,7-diphenyl-1,2,3,4,4a,5-hexahydro-10H-benzimidazo[2,1-j]quinolin-10-ylidene)malonamide
Synonyms: 2-(5,7-diphenyl-1,2,3,4,4a,5-hexahydro-10H-benzimidazo[2,1-j]quinolin-10-ylidene)malonamide
CAS NO:1206830-57-0
Molecular Formula:
Molecular Weight: 476.578
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-(5,7-diphenyl-1,2,3,4,4a,5-hexahydro-10H-benzimidazo[2,1-j]quinolin-10-ylidene)malonamide(CAS DataBase Reference)
NIST Chemistry Reference: 2-(5,7-diphenyl-1,2,3,4,4a,5-hexahydro-10H-benzimidazo[2,1-j]quinolin-10-ylidene)malonamide(1206830-57-0)
EPA Substance Registry System: 2-(5,7-diphenyl-1,2,3,4,4a,5-hexahydro-10H-benzimidazo[2,1-j]quinolin-10-ylidene)malonamide(1206830-57-0)

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: 1206830-57-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1206830-57-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,8,3 and 0 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1206830-57:
(9*1)+(8*2)+(7*0)+(6*6)+(5*8)+(4*3)+(3*0)+(2*5)+(1*7)=130
130 % 10 = 0
So 1206830-57-0 is a valid CAS Registry Number.

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1206830-57-0Relevant academic research and scientific papers

Oxidative coupling of substituted 1,2,3,4,4a,5-hexahydro-13H-benzimidazo[2, 1-j]quinolines with Methylene-active derivatives of carboxylic acids

Slabko, O. Yu.,Ageenko,Kaminskii

experimental part, p. 1214 - 1218 (2009/12/07)

The oxidative coupling of substituted 1,2,3,4,4a,5-hexahydro-13H- benzimidazo[2,1-j]quinolines with methylene-active derivatives of carboxylic acids led to the formation of p-methylenequinone imines of the mentioned series; in some events the reaction was

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