135041-23-5 Usage
Uses
Used in Pharmaceutical Research:
2-Amino-6-chloro-[(4-methylphenyl)thio]-9-(2’,3’,5’-tri-O-acetyl--D-ribofuranosyl)purine is used as a research compound for its potential antiviral and antitumor properties. It aids in the development of new drugs and therapeutic agents by providing insights into its interactions with biological systems and its effects on viral and tumor cells.
Used in Nucleoside Chemistry:
In the field of nucleoside chemistry, 2-Amino-6-chloro-[(4-methylphenyl)thio]-9-(2’,3’,5’-tri-O-acetyl--D-ribofuranosyl)purine serves as a key compound for understanding the structure and function of nucleosides. Its unique chemical features allow researchers to explore its reactivity, synthesis, and potential applications in the creation of new nucleoside analogs.
Used in Biochemistry:
2-Amino-6-chloro-[(4-methylphenyl)thio]-9-(2’,3’,5’-tri-O-acetyl--D-ribofuranosyl)purine is utilized in biochemistry to study its interactions with enzymes, proteins, and other biomolecules. This knowledge can help elucidate the mechanisms of action of 2-Amino-6-chloro-[(4-methylphenyl)thio]-9-(2’,3’,5’-tri-O-acetyl--D-ribofuranosyl)purine and its potential role in biological processes, leading to the discovery of new therapeutic targets and strategies.
Check Digit Verification of cas no
The CAS Registry Mumber 135041-23-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,5,0,4 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 135041-23:
(8*1)+(7*3)+(6*5)+(5*0)+(4*4)+(3*1)+(2*2)+(1*3)=85
85 % 10 = 5
So 135041-23-5 is a valid CAS Registry Number.
135041-23-5Relevant academic research and scientific papers
Conversion of Guanosine into Isoguanosine and Derivatives
Divakar, K. J.,Mottahedeh, Mina,Reese, Colin B.,Sanghvi, Yogesh S.,Swift, Karl A. D.
, p. 771 - 774 (2007/10/02)
Treatment of 2-amino-6-chloro-9-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)purine 7, which is readily prepared from guanosine 2 in two steps, with toluene-4-thiol and triethylamine followed by sodium nitrite in aqueous acetic acid gives 6-(4-methylphenyl)thio
