Cas 1609547-84-3,6'-chloro-4'-(3-oxobutyl)-1-tosyl-3',4'-dihydrospiro[piperidine-4,2'-pyrimido[1,2-a]pyrimidin]-8'-(1'H)-one

1609547-84-3

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Basic information

Product Name: 6'-chloro-4'-(3-oxobutyl)-1-tosyl-3',4'-dihydrospiro[piperidine-4,2'-pyrimido[1,2-a]pyrimidin]-8'-(1'H)-one
Synonyms: 6'-chloro-4'-(3-oxobutyl)-1-tosyl-3',4'-dihydrospiro[piperidine-4,2'-pyrimido[1,2-a]pyrimidin]-8'-(1'H)-one
CAS NO:1609547-84-3
Molecular Formula:
Molecular Weight: 479
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: 6'-chloro-4'-(3-oxobutyl)-1-tosyl-3',4'-dihydrospiro[piperidine-4,2'-pyrimido[1,2-a]pyrimidin]-8'-(1'H)-one(CAS DataBase Reference)
NIST Chemistry Reference: 6'-chloro-4'-(3-oxobutyl)-1-tosyl-3',4'-dihydrospiro[piperidine-4,2'-pyrimido[1,2-a]pyrimidin]-8'-(1'H)-one(1609547-84-3)
EPA Substance Registry System: 6'-chloro-4'-(3-oxobutyl)-1-tosyl-3',4'-dihydrospiro[piperidine-4,2'-pyrimido[1,2-a]pyrimidin]-8'-(1'H)-one(1609547-84-3)

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: 1609547-84-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1609547-84-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,0,9,5,4 and 7 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 1609547-84:
(9*1)+(8*6)+(7*0)+(6*9)+(5*5)+(4*4)+(3*7)+(2*8)+(1*4)=193
193 % 10 = 3
So 1609547-84-3 is a valid CAS Registry Number.

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1609547-84-3Relevant academic research and scientific papers

Carbon radical attack on a pyrimidine nitrogen. An unusual entry into polycyclic aminopyrimidones

Qin, Ling,Liu, Zhibo,Zard, Samir Z.

supporting information, p. 2966 - 2969 (2014/06/23)

Unprecedented examples of a synthetically useful radical ring closure onto a pyrimidine nitrogen leading to novel, highly functionalized bi- and tricyclic pyrimidone structures are reported. An unexpected hydrogen atom translocation prior to the cyclization step was observed in some cases.

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