161923-50-8 Usage
Uses
Used in Organic Synthesis:
6-Chloro-2-hydroxy-9-(2',3',5'-tri-O-acetyl-b-D-ribofuranosyl)purine is used as an intermediate in the synthesis of various organic compounds. Its unique structure allows it to be a valuable building block for the development of new molecules with potential applications in various fields, such as pharmaceuticals, agrochemicals, and materials science.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 6-Chloro-2-hydroxy-9-(2',3',5'-tri-O-acetyl-b-D-ribofuranosyl)purine is used as a key component in the development of novel therapeutic agents. Its chemical properties make it a promising candidate for the design of new drugs targeting various diseases, including cancer, viral infections, and neurological disorders.
Used in Research and Development:
6-Chloro-2-hydroxy-9-(2',3',5'-tri-O-acetyl-b-D-ribofuranosyl)purine is also utilized in research and development laboratories for the study of its chemical properties and potential applications. Scientists and researchers can use this compound to explore new reaction pathways, develop innovative synthetic methods, and gain insights into the structure-activity relationships of related molecules.
Check Digit Verification of cas no
The CAS Registry Mumber 161923-50-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,1,9,2 and 3 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 161923-50:
(8*1)+(7*6)+(6*1)+(5*9)+(4*2)+(3*3)+(2*5)+(1*0)=128
128 % 10 = 8
So 161923-50-8 is a valid CAS Registry Number.
161923-50-8Relevant articles and documents
Synthesis of 2-aralkoxyadenosines and 2-alkoxyadenosines
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Page/Page column 6, (2008/06/13)
The invention provides new methods for synthesis of 2-aralkyloxyadenosines and 2-alkoxyadenosines. The invention is particularly useful for synthesis of 2-[2-(4-chlorophenyl)ethoxy]adenosine. Preferred methods of the invention include activating a guanosine compound followed by hydrolysis; alkylating the hydrolyzed compound with subsequent animation to provide a 2-aralkyloxyadenosine or a 2-alkoxyadenosine compound.
Improved Synthesis of Isoguanosine and 6-Substituted Xanthosine Derivatives
Napoli, Lorenzo De,Montesarchio, Daniela,Piccialli, Gennaro,Santacroce, Ciro,Varra, Michela
, p. 15 - 18 (2007/10/02)
Isoguanosine 1 was obtained in 76percent overall yield starting from 2',3',5'-tri-O-acetylxanthosine 3 in a reaction involving the chloro derivative 4 and the N-(purin-6-yl)pyridinium salt derivative 8 which also proved to be new and valuable synthetic intermediates in the obtainment of C-6-substituted xanthosine derivatives.