Cas 1035587-75-7,3-benzyl-1-([4-(2-(methoxymethyl)pyrimidin-4-yl)piperazin-1-yl]sulfonyl)imidazolidine-2,4-dione

1035587-75-7

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Basic information

Product Name: 3-benzyl-1-([4-(2-(methoxymethyl)pyrimidin-4-yl)piperazin-1-yl]sulfonyl)imidazolidine-2,4-dione
Synonyms:
CAS NO:1035587-75-7
Molecular Formula:
Molecular Weight: 460.514
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: 3-benzyl-1-([4-(2-(methoxymethyl)pyrimidin-4-yl)piperazin-1-yl]sulfonyl)imidazolidine-2,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3-benzyl-1-([4-(2-(methoxymethyl)pyrimidin-4-yl)piperazin-1-yl]sulfonyl)imidazolidine-2,4-dione(1035587-75-7)
EPA Substance Registry System: 3-benzyl-1-([4-(2-(methoxymethyl)pyrimidin-4-yl)piperazin-1-yl]sulfonyl)imidazolidine-2,4-dione(1035587-75-7)

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: 1035587-75-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1035587-75-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,3,5,5,8 and 7 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1035587-75:
(9*1)+(8*0)+(7*3)+(6*5)+(5*5)+(4*8)+(3*7)+(2*7)+(1*5)=157
157 % 10 = 7
So 1035587-75-7 is a valid CAS Registry Number.

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1035587-75-7Relevant academic research and scientific papers

Synthesis and biological evaluations of new pyrrolo[2,3-b]pyrimidine as SDI analogs

Guillard, Jerome,Viaud-Massuard, Marie-Claude

, p. 1163 - 1189 (2008)

The synthesis of new pyrrolo[2,3-d]pyrimidines variously substituted on the N-1 and C-2 atoms are described. Access to these compounds, which have modest activity compared with the first inhibitor SDI, involves, as the key step, the formation of a pyrrolopyrimidine skeleton from the 5-amino-2-(methoxymethyl)pyrimidine.

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