Cas 98815-83-9,N-[9-((R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-{(R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-[(4-methoxy-phenyl)-diphenyl-methoxy]-ethoxy}-ethyl)-9H-purin-6-yl]-benzamide

98815-83-9

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Product Name: N-[9-((R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-{(R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-[(4-methoxy-phenyl)-diphenyl-methoxy]-ethoxy}-ethyl)-9H-purin-6-yl]-benzamide
Synonyms:
CAS NO:98815-83-9
Molecular Formula:
Molecular Weight: 874.24
EINECS: N/A
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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-[9-((R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-{(R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-[(4-methoxy-phenyl)-diphenyl-methoxy]-ethoxy}-ethyl)-9H-purin-6-yl]-benzamide(CAS DataBase Reference)
NIST Chemistry Reference: N-[9-((R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-{(R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-[(4-methoxy-phenyl)-diphenyl-methoxy]-ethoxy}-ethyl)-9H-purin-6-yl]-benzamide(98815-83-9)
EPA Substance Registry System: N-[9-((R)-2-(tert-Butyl-dimethyl-silanyloxy)-1-{(R)-1-(tert-butyl-dimethyl-silanyloxymethyl)-2-[(4-methoxy-phenyl)-diphenyl-methoxy]-ethoxy}-ethyl)-9H-purin-6-yl]-benzamide(98815-83-9)

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RTECS:
HazardClass: N/A
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Hazardous Substances Data: 98815-83-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 98815-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,8,8,1 and 5 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 98815-83:
(7*9)+(6*8)+(5*8)+(4*1)+(3*5)+(2*8)+(1*3)=189
189 % 10 = 9
So 98815-83-9 is a valid CAS Registry Number.

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98815-83-9Relevant academic research and scientific papers

SYNTHESIS OF A NEW CLASS OF ACYCLIC 2',5'- AND 3',5'-OLIGONUCLEOTIDE ANALOGS BASED ON 9--ADENINE

Mikhailov, Sergey N.,Pfleiderer, Wolfgang

, p. 2059 - 2062 (1985)

The acyclic analogs of 2',5'- and 3',5'-oligoadenylates possessing all functional groups of the natural compounds were prepared on the basis of "oxydized-reduced" adenosine.

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