Cas 1172613-01-2,5-(2-fluoro-3-trifluoromethylphenyl)-1,3-dimethyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione

1172613-01-2

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Basic information

Product Name: 5-(2-fluoro-3-trifluoromethylphenyl)-1,3-dimethyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione
Synonyms:
CAS NO:1172613-01-2
Molecular Formula:
Molecular Weight: 457.384
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: 5-(2-fluoro-3-trifluoromethylphenyl)-1,3-dimethyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione(CAS DataBase Reference)
NIST Chemistry Reference: 5-(2-fluoro-3-trifluoromethylphenyl)-1,3-dimethyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione(1172613-01-2)
EPA Substance Registry System: 5-(2-fluoro-3-trifluoromethylphenyl)-1,3-dimethyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione(1172613-01-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1172613-01-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1172613-01-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,7,2,6,1 and 3 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1172613-01:
(9*1)+(8*1)+(7*7)+(6*2)+(5*6)+(4*1)+(3*3)+(2*0)+(1*1)=122
122 % 10 = 2
So 1172613-01-2 is a valid CAS Registry Number.

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1172613-01-2Relevant academic research and scientific papers

Novel pyridopyrimidine derivatives as inhibitors of stable toxin a (STa) induced cGMP synthesis

Tanifum, Eric A.,Kots, Alexander Y.,Choi, Byung-Kwon,Murad, Ferid,Gilbertson, Scott R.

supporting information; experimental part, p. 3067 - 3071 (2010/01/16)

A series of pyridopyrimidine derivatives were synthesized and evaluated for their ability to inhibit cyclic nucleotide synthesis in the presence of stable toxin a of Escherichia coli. The structure activity relationships around the basic core structure we

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