132062-69-2 Usage
Uses
Used in Pharmaceutical and Medicinal Research:
[(2R,6R)-6-(6-amino-9H-purin-9-yl)-1,4-oxathian-2-yl]methanol is used as a compound of interest for its potential applications in drug development and molecular biology research. The complex structure and the presence of functional groups in the molecule allow for interactions with biological systems, which could be harnessed for therapeutic purposes.
Used in Drug Development:
In the pharmaceutical industry, [(2R,6R)-6-(6-amino-9H-purin-9-yl)-1,4-oxathian-2-yl]methanol is used as a starting material or a building block for the synthesis of novel drugs. Its unique structure and functional groups may be exploited to design and develop new therapeutic agents with specific biological activities.
Used in Molecular Biology Research:
In the field of molecular biology, [(2R,6R)-6-(6-amino-9H-purin-9-yl)-1,4-oxathian-2-yl]methanol may be used as a probe or a tool to study the interactions between biological molecules and cellular processes. Its potential biological activity could provide insights into the mechanisms of various diseases and contribute to the development of targeted therapies.
Check Digit Verification of cas no
The CAS Registry Mumber 132062-69-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,2,0,6 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 132062-69:
(8*1)+(7*3)+(6*2)+(5*0)+(4*6)+(3*2)+(2*6)+(1*9)=92
92 % 10 = 2
So 132062-69-2 is a valid CAS Registry Number.
132062-69-2Relevant academic research and scientific papers
NUCLEOSIDE ANALOGUES WITH A 1,4-DIOXANE, 1,4-OXATHIANE OR 1,4-OXAZINE RING STRUCTURE AS THE CARBOHYDRATE FRAGMENT
Aerschot, Arthur Van,Janssen, Gerard,Herdewijn, Piet
, p. 769 - 777 (2007/10/02)
Pyrimidine and purine nucleoside analogues with a 1,4-dioxane, 1,4-oxathiane or 1,4-oxazine ring structure have been prepared from the corresponding dimesylated seconucleosides by treatment with either sodium hydroxide, sodium sulfide or primary alkylamines.
