Cas 1310063-73-0,(2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(2-acetoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate

1310063-73-0

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Basic information

Product Name: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(2-acetoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate
Synonyms:
CAS NO:1310063-73-0
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: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(2-acetoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(CAS DataBase Reference)
NIST Chemistry Reference: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(2-acetoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(1310063-73-0)
EPA Substance Registry System: (2R,3R,4R,5R)-2-(acetoxymethyl)-5-(6-(2-acetoxyphenyl)-9H-purin-9-yl)tetrahydrofuran-3,4-diyl diacetate(1310063-73-0)

Safety Data

Hazard Codes: N/A
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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1310063-73-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1310063-73-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,0,0,6 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1310063-73:
(9*1)+(8*3)+(7*1)+(6*0)+(5*0)+(4*6)+(3*3)+(2*7)+(1*3)=90
90 % 10 = 0
So 1310063-73-0 is a valid CAS Registry Number.

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1310063-73-0Relevant academic research and scientific papers

Palladium-catalyzed C-H bond functionalization of C6-arylpurines

Guo, Hai-Ming,Rao, Wei-Hao,Niu, Hong-Ying,Jiang, Li-Li,Meng, Ge,Jin, Jia-Jia,Yang, Xi-Ning,Qu, Gui-Rong

supporting information; experimental part, p. 5608 - 5610 (2011/06/21)

A highly regioselective Pd-catalyzed CAr-H bond activation method was developed for the modification of purines (nucleosides) with different functional groups by using purine as a directing group. This approach provides a new access to a variet

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