Cas 325844-95-9,2-amino-5-benzoyl-4-methylsulfanyl-6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carbonitrile

325844-95-9

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Basic information

Product Name: 2-amino-5-benzoyl-4-methylsulfanyl-6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carbonitrile
Synonyms: 2-amino-5-benzoyl-4-methylsulfanyl-6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carbonitrile
CAS NO:325844-95-9
Molecular Formula:
Molecular Weight: 361.424
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-amino-5-benzoyl-4-methylsulfanyl-6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: 2-amino-5-benzoyl-4-methylsulfanyl-6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carbonitrile(325844-95-9)
EPA Substance Registry System: 2-amino-5-benzoyl-4-methylsulfanyl-6-oxo-1-phenyl-1,6-dihydro-pyridine-3-carbonitrile(325844-95-9)

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: 325844-95-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 325844-95-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,2,5,8,4 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 325844-95:
(8*3)+(7*2)+(6*5)+(5*8)+(4*4)+(3*4)+(2*9)+(1*5)=159
159 % 10 = 9
So 325844-95-9 is a valid CAS Registry Number.

325844-95-9Upstream product

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325844-95-9Relevant academic research and scientific papers

Synthesis of novel derivatives of 4-methylthio-N-aryl-2-pyridone and deazapurine analogues: The reaction of ketene dithioacetals with substituted acetanilides

Elgemeie, Galal H.,Ali, Hosny A.,Elghandour, Ahmed H.,Abd Elaziz, Ghada W.

, p. 189 - 197 (2007/10/03)

A new one-pot synthesis of 4-methylthio-N-aryl-2-pyridones and their deazapurine analogues by the reaction of ketene dithioacetals with substituted acetanilides have been reported.

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