138509-92-9 Usage
Uses
Used in Research Applications:
Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-3'-O-(trimethylsilyl)is used as a research tool for studying the structure, function, and interactions of uridine and its derivatives in biological systems. The chemical modifications in Uridine,
5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-3'-O-(trimethylsilyl)- can provide insights into the role of specific functional groups in modulating the properties and activities of uridine.
Used in Pharmaceutical Applications:
Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-3'-O-(trimethylsilyl)is used as a potential therapeutic agent in the development of drugs targeting uridine-related processes in the body. The chemical modifications in Uridine,
5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-3'-O-(trimethylsilyl)- may enhance its stability, solubility, and interactions with other molecules, making it a promising candidate for drug discovery and development.
Used in Drug Delivery Systems:
In the pharmaceutical industry, Uridine, 5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-3'-O-(trimethylsilyl)can be used as a component of drug delivery systems to improve the bioavailability and therapeutic efficacy of uridine and its derivatives. The chemical modifications in Uridine,
5'-O-[bis(4-methoxyphenyl)phenylmethyl]-2'-deoxy-3'-O-(trimethylsilyl)- may facilitate its encapsulation, release, and targeting to specific tissues or cells, enhancing its potential as a drug delivery vehicle.
Check Digit Verification of cas no
The CAS Registry Mumber 138509-92-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,8,5,0 and 9 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 138509-92:
(8*1)+(7*3)+(6*8)+(5*5)+(4*0)+(3*9)+(2*9)+(1*2)=149
149 % 10 = 9
So 138509-92-9 is a valid CAS Registry Number.
138509-92-9Relevant academic research and scientific papers
Commercial-scale synthesis of protected 2′-deoxycytidine and cytidine nucleosides
Divakar, Kikkeri J.,Sawant, Chitra M.,Mulla,Zemse, Deepak V.,Sitabkhan, Sakina M.,Ross, Bruce S.,Sanghvi, Yogesh S.
, p. 1321 - 1325 (2007/10/03)
Transformation of 2′-deoxyuridine and uridine analogs to protected 2′-deoxycytidine and cytidine analogs has been investigated by two different methods. First, traditional triazolation protocol and second p-nitrophenoxylation method. Our studies conclude
