Cas 740801-34-7,<i>N</i>-{1-[(cyclohexyl-methanesulfonyl-amino)-methyl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide

740801-34-7

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Basic information

Product Name: N-{1-[(cyclohexyl-methanesulfonyl-amino)-methyl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide
Synonyms: N-{1-[(cyclohexyl-methanesulfonyl-amino)-methyl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide
CAS NO:740801-34-7
Molecular Formula:
Molecular Weight: 404.49
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: N-{1-[(cyclohexyl-methanesulfonyl-amino)-methyl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-{1-[(cyclohexyl-methanesulfonyl-amino)-methyl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide(740801-34-7)
EPA Substance Registry System: N-{1-[(cyclohexyl-methanesulfonyl-amino)-methyl]-2-oxo-1,2-dihydro-pyrimidin-4-yl}-benzamide(740801-34-7)

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: 740801-34-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 740801-34-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,4,0,8,0 and 1 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 740801-34:
(8*7)+(7*4)+(6*0)+(5*8)+(4*0)+(3*1)+(2*3)+(1*4)=137
137 % 10 = 7
So 740801-34-7 is a valid CAS Registry Number.

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740801-34-7Relevant academic research and scientific papers

Facile synthesis of acyclic azanucleosides from N-pivaloyloxymethyl amides and sulfonamides: Synthesis of aza-analogues of Ganciclovir

Koszytkowska-Stawińska, Mariola,Sas, Wojciech

, p. 5437 - 5440 (2007/10/03)

N-Pivaloyloxymethyl amides and sulfonamides, readily available from N-alkylation of both amides and sulfonamides with commercial chloromethyl pivaloate, were converted into acyclic azanucleosides via a one-pot base silylation/nucleoside coupling procedure

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