Cas 332382-63-5,5-(3-bromophenyl)-1-methyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione

332382-63-5

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Basic information

Product Name: 5-(3-bromophenyl)-1-methyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione
Synonyms:
CAS NO:332382-63-5
Molecular Formula:
Molecular Weight: 436.264
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-(3-bromophenyl)-1-methyl-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-(3-bromophenyl)-1-methyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione(332382-63-5)
EPA Substance Registry System: 5-(3-bromophenyl)-1-methyl-5,11-dihydro-1H-indeno-[2',1':5,6]pyrido[2,3-d]pyrimidine-2,3,6-trione(332382-63-5)

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: 332382-63-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 332382-63-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,3,2,3,8 and 2 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 332382-63:
(8*3)+(7*3)+(6*2)+(5*3)+(4*8)+(3*2)+(2*6)+(1*3)=125
125 % 10 = 5
So 332382-63-5 is a valid CAS Registry Number.

332382-63-5Upstream product

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332382-63-5Relevant 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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