Cas 1227733-63-2,5-(4-methoxyphenyl)-9-thioxo-1,2,3,4,5,6,6a,7,8,9,10,12-dodecahydrodipyrimido[4,5-b;5',4'-g][1,8]naphthyridine-2,4,6,7-tetraone

1227733-63-2

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Basic information

Product Name: 5-(4-methoxyphenyl)-9-thioxo-1,2,3,4,5,6,6a,7,8,9,10,12-dodecahydrodipyrimido[4,5-b;5',4'-g][1,8]naphthyridine-2,4,6,7-tetraone
Synonyms:
CAS NO:1227733-63-2
Molecular Formula:
Molecular Weight: 438.423
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-(4-methoxyphenyl)-9-thioxo-1,2,3,4,5,6,6a,7,8,9,10,12-dodecahydrodipyrimido[4,5-b;5',4'-g][1,8]naphthyridine-2,4,6,7-tetraone(CAS DataBase Reference)
NIST Chemistry Reference: 5-(4-methoxyphenyl)-9-thioxo-1,2,3,4,5,6,6a,7,8,9,10,12-dodecahydrodipyrimido[4,5-b;5',4'-g][1,8]naphthyridine-2,4,6,7-tetraone(1227733-63-2)
EPA Substance Registry System: 5-(4-methoxyphenyl)-9-thioxo-1,2,3,4,5,6,6a,7,8,9,10,12-dodecahydrodipyrimido[4,5-b;5',4'-g][1,8]naphthyridine-2,4,6,7-tetraone(1227733-63-2)

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: 1227733-63-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1227733-63-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,7,3 and 3 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1227733-63:
(9*1)+(8*2)+(7*2)+(6*7)+(5*7)+(4*3)+(3*3)+(2*6)+(1*3)=152
152 % 10 = 2
So 1227733-63-2 is a valid CAS Registry Number.

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1227733-63-2Relevant academic research and scientific papers

Facile and one pot synthetic routes for various novel, differently fused and promising heteropolycycles

Gupta, Shallu,Gupta, Poonam,Sachar, Anand,Sharma

experimental part, p. 334 - 349 (2010/05/19)

(Chemical Equation Presented) Four-component one pot cyclocondensation of aromatic aldehydes 1, ethyl cyanoacetate 2, barbituric acid 3 and ammonium acetate in methanol gave substituted and functionalised pyrido[2,3-d]pyrimidine derivatives 4 and 4′ after

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