Cas 1256151-00-4,ethyl 10-chloro-9-fluoro-4-methyl-7-oxo-6-phenyl-1,2,6,7-tetrahydrobenzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-5-carboxylate

1256151-00-4

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Basic information

Product Name: ethyl 10-chloro-9-fluoro-4-methyl-7-oxo-6-phenyl-1,2,6,7-tetrahydrobenzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-5-carboxylate
Synonyms:
CAS NO:1256151-00-4
Molecular Formula:
Molecular Weight: 438.886
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: ethyl 10-chloro-9-fluoro-4-methyl-7-oxo-6-phenyl-1,2,6,7-tetrahydrobenzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-5-carboxylate(CAS DataBase Reference)
NIST Chemistry Reference: ethyl 10-chloro-9-fluoro-4-methyl-7-oxo-6-phenyl-1,2,6,7-tetrahydrobenzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-5-carboxylate(1256151-00-4)
EPA Substance Registry System: ethyl 10-chloro-9-fluoro-4-methyl-7-oxo-6-phenyl-1,2,6,7-tetrahydrobenzo[b]imidazo[1,2,3-ij][1,8]naphthyridine-5-carboxylate(1256151-00-4)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1256151-00-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1256151-00-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,1,5 and 1 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1256151-00:
(9*1)+(8*2)+(7*5)+(6*6)+(5*1)+(4*5)+(3*1)+(2*0)+(1*0)=124
124 % 10 = 4
So 1256151-00-4 is a valid CAS Registry Number.

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1256151-00-4Relevant academic research and scientific papers

Modulating the reactivity of heterocyclic ketene aminals in MCR: Selective construction of tetrahydrobenzo[ b ]imidazo[3,2,1- ij ][1,8]naphthyridines

Wen, Li-Rong,Liu, Chao,Li, Ming,Wang, Li-Juan

, p. 7605 - 7614 (2010)

Two new kinds of tetrahydrobenzo[b]imidazo[3,2,1-ij][1,8]naphthyridine derivatives have been successfully synthesized by cascade reactions including Knoevenagel condensation, aza-ene reaction, imine-enamine tautomerization, cyclocondensation, and intramol

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