Cas 946530-65-0,(1R,3R,4R,7S)-7-benzyloxy-5-tert-butoxycarbonyl-1-hydroxymethyl-3-(adenin-9-yl)-2-oxa-5-azabicyclo[2.2.1]heptane

946530-65-0

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Basic information

Product Name: (1R,3R,4R,7S)-7-benzyloxy-5-tert-butoxycarbonyl-1-hydroxymethyl-3-(adenin-9-yl)-2-oxa-5-azabicyclo[2.2.1]heptane
Synonyms: (1R,3R,4R,7S)-7-benzyloxy-5-tert-butoxycarbonyl-1-hydroxymethyl-3-(adenin-9-yl)-2-oxa-5-azabicyclo[2.2.1]heptane
CAS NO:946530-65-0
Molecular Formula:
Molecular Weight: 468.513
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: (1R,3R,4R,7S)-7-benzyloxy-5-tert-butoxycarbonyl-1-hydroxymethyl-3-(adenin-9-yl)-2-oxa-5-azabicyclo[2.2.1]heptane(CAS DataBase Reference)
NIST Chemistry Reference: (1R,3R,4R,7S)-7-benzyloxy-5-tert-butoxycarbonyl-1-hydroxymethyl-3-(adenin-9-yl)-2-oxa-5-azabicyclo[2.2.1]heptane(946530-65-0)
EPA Substance Registry System: (1R,3R,4R,7S)-7-benzyloxy-5-tert-butoxycarbonyl-1-hydroxymethyl-3-(adenin-9-yl)-2-oxa-5-azabicyclo[2.2.1]heptane(946530-65-0)

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: 946530-65-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 946530-65-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,4,6,5,3 and 0 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 946530-65:
(8*9)+(7*4)+(6*6)+(5*5)+(4*3)+(3*0)+(2*6)+(1*5)=190
190 % 10 = 0
So 946530-65-0 is a valid CAS Registry Number.

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946530-65-0Relevant academic research and scientific papers

ADENOSINE RECEPTOR ANTAGONISTS

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Page/Page column 31; Sheet 2, (2008/06/13)

The present application discloses locked nucleoside compounds of the Formula I which act as antagonists of adenosine receptors, in particular the adenosine A3 receptor, and the use of such adenosine A3 receptor compounds in medicine, e.g. for the treatmen

Design, synthesis, and biological evaluation of LNA nucleosides as adenosine A3 receptor ligands

Ravn, Jacob,Qvortrup, Katrine,Rosenbohm, Christoph,Koch, Troels

, p. 5440 - 5447 (2008/03/18)

We have prepared a series of adenosine analogs based on the bicyclo[2.2.1]heptane scaffold of locked nucleic acid (LNA) and tested them for both agonist and antagonist activity at the adenosine A3 receptor. The design of these derivatives was b

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