71519-70-5 Usage
Uses
Used in Pharmaceutical Industry:
1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol is used as a potential drug candidate for its antiviral and antifungal properties, making it a promising compound for the development of new treatments for various diseases.
Used in Antiviral Applications:
1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol is used as an antiviral agent due to its potential to inhibit viral replication and reduce the severity of viral infections.
Used in Antifungal Applications:
1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol is used as an antifungal agent for its ability to combat fungal infections and prevent the growth of fungi.
Further research is required to explore the full potential of 1-(2-amino-1,3-thiazol-5-yl)-1,4-anhydropentitol in various applications and to optimize its use in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 71519-70-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,1,5,1 and 9 respectively; the second part has 2 digits, 7 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 71519-70:
(7*7)+(6*1)+(5*5)+(4*1)+(3*9)+(2*7)+(1*0)=125
125 % 10 = 5
So 71519-70-5 is a valid CAS Registry Number.
71519-70-5Relevant academic research and scientific papers
A short and highly stereoselective synthesis of α-(2-aminothiazolyl)-C-nucleosides
Navarre, Jean-Michel,Guianvarc'h, Dominique,Farese-Di Giorgio, Audrey,Condom, Roger,Benhida, Rachid
, p. 2199 - 2202 (2007/10/03)
A short route to novel α-(2-aminothiazolyl)-C-nucleosides has been developed. The key step was the high diastereoselective reduction of the hemiacetal intermediates using L-Selectride, which afforded the corresponding R-diols in quantitative yields. These diols were converted, after C4-C1 ring closure and protecting groups cleavage, to their corresponding free α-C-nucleosides.
Efficient stereoselective synthesis of new C-nucleosides via intramolecular Mitsunobu cyclization
Benhida,Guianvarch,Fourrey,Sun
, p. 603 - 604 (2007/10/03)
We have studied the stereoselective synthesis of new C-nucleosides by heteroarylation of the protected γ-ribonolactone by means of heteroaromatic systems such as indole, thiazoles, imidazoles and benzimidazoles. We have observed that the first anion addit