20838-22-6 Usage
Description
3'-O,5'-O-Dibenzoyl-2'-deoxyadenosine is a chemical compound that serves as an intermediate in the synthesis of various organic compounds. It is characterized by its unique structure, which includes a deoxyadenosine molecule with a 2'-deoxyribose sugar moiety and two benzoyl groups attached to the 3' and 5' positions.
Uses
Used in Organic Synthesis:
3'-O,5'-O-Dibenzoyl-2'-deoxyadenosine is used as an intermediate in the synthesis of 1,3,5-Tri-O-benzoyl-2-deoxyribofuranose (T767660), a compound that is valuable in organic synthesis. This intermediate plays a crucial role in the development of new chemical compounds and materials.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3'-O,5'-O-Dibenzoyl-2'-deoxyadenosine is used as a building block for the development of new drugs. Its unique structure and properties make it a promising candidate for the creation of novel therapeutic agents.
Used in Research and Development:
3'-O,5'-O-Dibenzoyl-2'-deoxyadenosine is also utilized in research and development settings, where it can be employed to study the properties and interactions of various biological molecules. 3'-O,5'-O-Dibenzoyl-2'-deoxyadenosine can be used to investigate the mechanisms of action of different drugs and to develop a better understanding of their effects on biological systems.
Check Digit Verification of cas no
The CAS Registry Mumber 20838-22-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,8,3 and 8 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 20838-22:
(7*2)+(6*0)+(5*8)+(4*3)+(3*8)+(2*2)+(1*2)=96
96 % 10 = 6
So 20838-22-6 is a valid CAS Registry Number.
20838-22-6Relevant articles and documents
Mild, efficient, selective and "green" benzoylation of nucleosides using benzoyl cyanide in ionic liquid
Prasad, Ashok K.,Kumar, Vineet,Maity, Jyotirmoy,Sanghvi, Yogesh S.,Ravikumar, Vasulinga T.,Parmar, Virinder S.
, p. 747 - 751 (2005)
Use of benzoyl cyanide (BzCN) for benzoylation of nucleosides has been studied, both in pyridine and in ionic liquid. BzCN in 1-methoxyethyl-3- methylimidazolium methanesulfonate as ionic liquid has been found to be a "green" alternative compared to the pyridine-BzCN system. An efficient and selective benzoylation of nucleosides of both, the 2′-deoxy- and the ribo-series at ambient temperature was accomplished. Copyright Taylor & Francis, Inc.
Enhanced solubility and selective benzoylation of nucleosides in novel ionic liquid
Kumar, Vineet,Parmar, Virinder S.,Malhotra, Sanjay V.
, p. 809 - 812 (2007)
Solubility and benzoylation study of both ribo- and deoxyribonucleosides is reported in a new ionic liquid MoeMIM·TFA; high selectivity for O-benzoylation is achieved.
Continuous flow photocatalysis enhanced using an aluminum mirror: Rapid and selective synthesis of 2′-deoxy and 2′,3′-dideoxynucleosides
Shen, Bo,Bedore, Matthew W.,Sniady, Adam,Jamison, Timothy F.
supporting information; experimental part, p. 7444 - 7446 (2012/10/08)
A unique photochemical flow reactor featuring quartz tubing, an aluminum mirror and temperature control has been developed for the photo-induced electron-transfer deoxygenation reaction to produce 2′-deoxy and 2′,3′-dideoxynucleosides. The continuous flow format significantly increased the efficiency and selectivity of the reaction.
