Cas 1006726-22-2,2-acetylamino-6-diphenylcarbamoyloxy-9-[N-(2-pivaloyloxyethyl)-p-toluenesulfonylaminomethyl]-9H-purine

1006726-22-2

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Basic information

Product Name: 2-acetylamino-6-diphenylcarbamoyloxy-9-[N-(2-pivaloyloxyethyl)-p-toluenesulfonylaminomethyl]-9H-purine
Synonyms: 2-acetylamino-6-diphenylcarbamoyloxy-9-[N-(2-pivaloyloxyethyl)-p-toluenesulfonylaminomethyl]-9H-purine
CAS NO:1006726-22-2
Molecular Formula:
Molecular Weight: 699.787
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: 2-acetylamino-6-diphenylcarbamoyloxy-9-[N-(2-pivaloyloxyethyl)-p-toluenesulfonylaminomethyl]-9H-purine(CAS DataBase Reference)
NIST Chemistry Reference: 2-acetylamino-6-diphenylcarbamoyloxy-9-[N-(2-pivaloyloxyethyl)-p-toluenesulfonylaminomethyl]-9H-purine(1006726-22-2)
EPA Substance Registry System: 2-acetylamino-6-diphenylcarbamoyloxy-9-[N-(2-pivaloyloxyethyl)-p-toluenesulfonylaminomethyl]-9H-purine(1006726-22-2)

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: 1006726-22-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1006726-22-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,6,7,2 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1006726-22:
(9*1)+(8*0)+(7*0)+(6*6)+(5*7)+(4*2)+(3*6)+(2*2)+(1*2)=112
112 % 10 = 2
So 1006726-22-2 is a valid CAS Registry Number.

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1006726-22-2Relevant academic research and scientific papers

Synthesis and antiviral properties of aza-analogues of Acyclovir

Koszytkowska-Stawinska, Mariola,Kaleta, Katarzyna,Sas, Wojciech,De Clercq, Erik

, p. 51 - 64 (2008/02/02)

Aza-analogues of Acyclovir were obtained from N-(2-pivaloyloxyethyl)-N- (pivaloyloxymethyl)-p-toluenesulfonamide via a one-pot base silylation/ nucleoside coupling procedure. The antiviral activities of all aza-nucleosides in vitro against a variety of vi

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