15569-30-9 Usage
Uses
Used in Biochemical Research:
Inosine, cyclic 2',3'-(hydrogen phosphate) (8CI,9CI) is used as a research tool for studying RNA structure and function. Its unique cyclic structure allows scientists to investigate the interactions between RNA molecules and other cellular components, providing insights into the fundamental mechanisms of gene expression and regulation.
Used in Pharmaceutical Development:
Inosine, cyclic 2',3'-(hydrogen phosphate) (8CI,9CI) has potential applications in the development of pharmaceuticals. Its involvement in the regulation of gene expression and protein synthesis makes it a promising candidate for the treatment of various diseases and conditions. Researchers are exploring its potential as a therapeutic agent, targeting specific biological pathways to modulate cellular processes and improve health outcomes.
Used in Biotechnology Products:
Inosine, cyclic 2',3'-(hydrogen phosphate) (8CI,9CI) also has potential applications in the development of biotechnology products. Its unique properties and ability to interact with RNA molecules make it a valuable component in the creation of novel diagnostic tools, therapeutic agents, and other biotechnological applications. By harnessing the power of Inosine, cyclic2',3'-(hydrogen phosphate) (8CI,9CI), scientists can develop innovative solutions to address various challenges in the fields of medicine, agriculture, and environmental science.
Check Digit Verification of cas no
The CAS Registry Mumber 15569-30-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,5,6 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 15569-30:
(7*1)+(6*5)+(5*5)+(4*6)+(3*9)+(2*3)+(1*0)=119
119 % 10 = 9
So 15569-30-9 is a valid CAS Registry Number.
15569-30-9Relevant academic research and scientific papers
SYNTHESIS OF 2'(3')-PHOSPHATES AND 2'(3')-PHOSPHOROTHIOATES OF 5'-O-CARBOXYMETHYLINOSINE AND RELATED COMPOUNDS
Holy, Antonin,Kois, Pavol
, p. 2817 - 2829 (2007/10/02)
5'-O-Carboxymethylinosine (IX) was prepared from disodium salt of 2',3'-O-isopropylideneinosine (VIII) by treatment with sodium chloroacetate, followed by acid hydrolysis. 5'-O-(2-Aminoethylamidocarbonylmethyl)inosine (XIII) was obtained by reaction of IX with p-nitrophenol and subsequent treatment with ethylenediamine.Action of triethyl phosphite on the compounds IX and XIII afforded the corresponding 5'-O-substituted 2'(3')-phosphites X and XIV which on reaction with trimethylsilyl chloride and sulfur gave the 2'(3')-phosphorothioates XI and XV.The compound IX was transformed by phosphorus oxychloride in 5'-O-carboxymethylinosine 2'(3')-phosphate (XII).Uridine, adenosine and inosine 2'(3')-phosphorothioates (Ia-Ic) were obtained from 2',3'-O-di-n-butylstannylene derivatives of the nucleosides IV by treatment with thiophosphoryl chloride followed by alkaline hydrolysis; inosine and guanosine 2'(3')-phosphorothioates (Ic, Id) were prepared by reaction of the corresponding 2'(3')-phosphites VIc, VId with trimethylsilyl chloride and sulfur.Cyclisation of Ic and Id with ethyl chloroformate in the presence of tri-n-butylamine afforded inosine 2',3'-O,O-cyclophosphorothioate (VIIc) and the corresponding guanosine derivative VIId.Compounds VIIc and VIId are not cleaved by Streptomyces aureofaciens ribonuclease.
