58048-26-3 Usage
Uses
Used in Pharmaceutical Industry:
(2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-(ethylcarbamoyl)tetrahydrofuran-3,4-diyl diacetate (non-preferred name) is used as a pharmaceutical compound for its potential therapeutic applications. The presence of the amino-purine group suggests it may have activity related to purine metabolism or nucleic acid synthesis, which could be harnessed for the development of drugs targeting specific diseases or conditions.
Used in Chemical Research:
In the field of chemical research, (2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-(ethylcarbamoyl)tetrahydrofuran-3,4-diyl diacetate (non-preferred name) serves as a subject for studying the synthesis and properties of complex organic molecules. Its unique structure and functional groups can provide insights into the reactivity and potential applications of similar compounds, contributing to the advancement of organic chemistry and related fields.
Please note that without specific details on the uses of (2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-(ethylcarbamoyl)tetrahydrofuran-3,4-diyl diacetate (non-preferred name) from the provided materials, the applications listed above are speculative and based on the general properties and structural features of the compound. Further research and information would be required to confirm its actual uses in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 58048-26-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,8,0,4 and 8 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 58048-26:
(7*5)+(6*8)+(5*0)+(4*4)+(3*8)+(2*2)+(1*6)=133
133 % 10 = 3
So 58048-26-3 is a valid CAS Registry Number.
58048-26-3Relevant articles and documents
Modification of the 5' Position of Purine Nucleosides. 2. Synthesis and Some Cardiovascular Properties of Adenosine-5'-(N-substituted)carboxamides
Prasad, Raj Nandan,Bariana, Dilbagh S.,Fung, Anthony,Savic, Milica,Tietje, Karin,et al.
, p. 313 - 319 (2007/10/02)
We have shown previously that the esters of adenosine-5'-carboxylic acid (10) represent a new class of potent nontoxic coronary vasodilators.For example, the ethyl ester (12), which is active by an intraduodenal or intravenous route in dogs, causes a larg