Cas 1357486-91-9,N<sub>6</sub>,N<sub>6</sub>-dibenzylformamidine-5'-O-[diethyl(ethoxycarbonyl)phosphonomethyl]-2',3'-O-isopropylidene adenosine

1357486-91-9

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Basic information

Product Name: N₆,N₆-dibenzylformamidine-5'-O-[diethyl(ethoxycarbonyl)phosphonomethyl]-2',3'-O-isopropylidene adenosine
Synonyms: N₆,N₆-dibenzylformamidine-5'-O-[diethyl(ethoxycarbonyl)phosphonomethyl]-2',3'-O-isopropylidene adenosine
CAS NO:1357486-91-9
Molecular Formula:
Molecular Weight: 736.762
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: N₆,N₆-dibenzylformamidine-5'-O-[diethyl(ethoxycarbonyl)phosphonomethyl]-2',3'-O-isopropylidene adenosine(CAS DataBase Reference)
NIST Chemistry Reference: N₆,N₆-dibenzylformamidine-5'-O-[diethyl(ethoxycarbonyl)phosphonomethyl]-2',3'-O-isopropylidene adenosine(1357486-91-9)
EPA Substance Registry System: N₆,N₆-dibenzylformamidine-5'-O-[diethyl(ethoxycarbonyl)phosphonomethyl]-2',3'-O-isopropylidene adenosine(1357486-91-9)

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: 1357486-91-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1357486-91-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,5,7,4,8 and 6 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1357486-91:
(9*1)+(8*3)+(7*5)+(6*7)+(5*4)+(4*8)+(3*6)+(2*9)+(1*1)=199
199 % 10 = 9
So 1357486-91-9 is a valid CAS Registry Number.

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1357486-91-9Relevant academic research and scientific papers

Development of O-H insertion for the attachment of phosphonates to nucleosides; Synthesis of α-carboxy phosphononucleosides

Hladezuk, Isabelle,Chastagner, Veronique,Collins, Stuart G.,Plunkett, Stephen J.,Ford, Alan,Debarge, Sebastien,Maguire, Anita R.

, p. 1894 - 1909 (2012/03/26)

Development of rhodium catalysed O-H insertion reactions employing α-diazophosphonates with appropriately protected adenosine, uridine and thymidine derivatives is described. This synthetic methodology leads, following deprotection, to novel phosphononucl

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