Cas 470485-39-3,4-[4-(4-methoxy-phenyl)-3-methyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl]-6-p-tolyl-4,5-dihydro-2H-pyridazin-3-one

470485-39-3

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Basic information

Product Name: 4-[4-(4-methoxy-phenyl)-3-methyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl]-6-p-tolyl-4,5-dihydro-2H-pyridazin-3-one
Synonyms:
CAS NO:470485-39-3
Molecular Formula:
Molecular Weight: 534.641
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: 4-[4-(4-methoxy-phenyl)-3-methyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl]-6-p-tolyl-4,5-dihydro-2H-pyridazin-3-one(CAS DataBase Reference)
NIST Chemistry Reference: 4-[4-(4-methoxy-phenyl)-3-methyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl]-6-p-tolyl-4,5-dihydro-2H-pyridazin-3-one(470485-39-3)
EPA Substance Registry System: 4-[4-(4-methoxy-phenyl)-3-methyl-1-phenyl-1H-pyrazolo[3,4-d]pyrimidin-6-ylsulfanyl]-6-p-tolyl-4,5-dihydro-2H-pyridazin-3-one(470485-39-3)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 470485-39-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 470485-39-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,7,0,4,8 and 5 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 470485-39:
(8*4)+(7*7)+(6*0)+(5*4)+(4*8)+(3*5)+(2*3)+(1*9)=163
163 % 10 = 3
So 470485-39-3 is a valid CAS Registry Number.

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470485-39-3Relevant academic research and scientific papers

Synthesis and reactions of new substituted pyrimidine thione derivatives as antimicrobial agents

Abd El-Ghaffar, Nahed F.,Kassab, Rafika R. S.,Soliman, Fekria M. A.

, p. 535 - 542 (2007/10/03)

Pyrimidinethiones containing also other heterocyclic moieties are known to exhibit vaned biological and pharmacological properties. In view of these observations, the present work describes the synthesis of some new substituted pyrimidine thiones starting from α, β-unsaturated carbonyl compounds and their antimicrobial activities. An attempt is made to study the structural activity relationships.

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