85335-73-5 Usage
Uses
Used in Research and Laboratory Applications:
Adenosine, N-acetyl-3',5'-O-[1,1,3,3-tetrakis(1-Methylethyl)-1,3-disiloxanediyl]is used as a research chemical for various scientific investigations due to its unique structure and properties. It aids in understanding biochemical processes and interactions within complex biological systems.
Used in Pharmaceutical Research:
In the pharmaceutical industry, Adenosine, N-acetyl-3',5'-O-[1,1,3,3-tetrakis(1-Methylethyl)-1,3-disiloxanediyl]is used as a compound for drug development and discovery. Its potential role in modulating biological responses makes it a candidate for the creation of new therapeutic agents.
Used in Chemical Synthesis:
Adenosine, N-acetyl-3',5'-O-[1,1,3,3-tetrakis(1-Methylethyl)-1,3-disiloxanediyl]is utilized as a building block or intermediate in the synthesis of more complex molecules, particularly in the fields of organic and medicinal chemistry.
Used in Material Science:
In material science, Adenosine, N-acetyl-3',5'-O-[1,1,3,3-tetrakis(1-Methylethyl)-1,3-disiloxanediyl]- may be explored for its potential applications in the development of new materials with specific properties, such as those with unique electronic or mechanical characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 85335-73-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,5,3,3 and 5 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 85335-73:
(7*8)+(6*5)+(5*3)+(4*3)+(3*5)+(2*7)+(1*3)=145
145 % 10 = 5
So 85335-73-5 is a valid CAS Registry Number.
85335-73-5Relevant academic research and scientific papers
NUCLEIC ACID RELATED COMPOUNDS. 42. A GENERAL PROCEDURE FOR THE EFFICIENT DEOXYGENATION OF SECONDARY ALCOHOLS. REGIOSPECIFIC AND STEREOSELECTIVE CONVERSION OF RIBONUCLEOSIDES TO 2 prime -DEOXYNUCLEOSIDES.
Robins,Wilson,Hansske
, p. 4059 - 4065 (2007/10/02)
Treatment of unhindered secondary alcohols with phenoxythiocarbonyl chloride (phenyl chlorothionocarbonate) in pyridine/dichloromethane, or in acetonitrile with 4-dimethylaminopyridine catalysis for hindered alcohols, gave clean conversion to their O-phenoxythiocarbonyl derivatives. Reductive deoxygenation of these phenyl thionocarbonate esters proceeded smoothly, using tri-n-butyltin hydride and a free radical initiator in warm toluene. Overall conversion yields ranged from 57 to 78% for the naturally occurring nucleosides, nucleoside antibiotics, and methyl beta -D-ribofuranoside.
