Cas 915022-17-2,Benzoic acid 9-((2S,3S,4S,5S)-3,4-diacetoxy-5-acetoxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylmethyl ester

915022-17-2

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Basic information

Product Name: Benzoic acid 9-((2S,3S,4S,5S)-3,4-diacetoxy-5-acetoxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylmethyl ester
Synonyms: Benzoic acid 9-((2S,3S,4S,5S)-3,4-diacetoxy-5-acetoxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylmethyl ester
CAS NO:915022-17-2
Molecular Formula:
Molecular Weight: 512.476
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: Benzoic acid 9-((2S,3S,4S,5S)-3,4-diacetoxy-5-acetoxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylmethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: Benzoic acid 9-((2S,3S,4S,5S)-3,4-diacetoxy-5-acetoxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylmethyl ester(915022-17-2)
EPA Substance Registry System: Benzoic acid 9-((2S,3S,4S,5S)-3,4-diacetoxy-5-acetoxymethyl-tetrahydro-furan-2-yl)-9H-purin-6-ylmethyl ester(915022-17-2)

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: 915022-17-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 915022-17-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,5,0,2 and 2 respectively; the second part has 2 digits, 1 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 915022-17:
(8*9)+(7*1)+(6*5)+(5*0)+(4*2)+(3*2)+(2*1)+(1*7)=132
132 % 10 = 2
So 915022-17-2 is a valid CAS Registry Number.

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915022-17-2Relevant academic research and scientific papers

Cytostatic and antiviral 6-arylpurine ribonucleosides. Part 7: Synthesis and evaluation of 6-substituted purine l-ribonucleosides

Hocek, Michal,Silhar, Peter,Shih, I-hung,Mabery, Eric,Mackman, Richard

, p. 5290 - 5293 (2007/10/03)

A series of purine l-ribonucleosides 2a-2i bearing diverse C-substituents (alkyl, aryl, hetaryl or hydroxymethyl) in the position 6 were prepared by Pd-catalyzed cross-coupling reactions of 6-chloro-9-(2,3,5-tri-O-acetyl-β-l-ribofuranosyl)purine with the

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