63202-26-6 Usage
Uses
Used in Pharmaceutical Industry:
1-(2',3',5'-tri-O-acetyl-α-D-ribofuranosyl)indazole is used as a compound with potential applications in medicinal chemistry and drug development. Its presence in the indazole class suggests it may exhibit biological activities such as antiviral, antibacterial, and anticancer properties, making it a promising candidate for further research and development.
Used in Medicinal Chemistry Research:
1-(2',3',5'-tri-O-acetyl-α-D-ribofuranosyl)indazole is used as a subject of study in medicinal chemistry, where its structure and properties are investigated for possible therapeutic applications. The acetylation of the ribofuranosyl group may enhance the compound's stability and pharmacokinetic properties, which could be beneficial in the development of new drugs.
Used in Drug Development:
1-(2',3',5'-tri-O-acetyl-α-D-ribofuranosyl)indazole is used as a starting point for the development of new drugs, particularly those targeting viral, bacterial, and cancer-related conditions. 1-(2',3',5'-tri-O-acetyl-α-D-ribofuranosyl)indazole's potential biological activities and its enhanced stability due to the acetylated ribofuranosyl group make it an attractive candidate for further exploration and optimization in the drug development process.
Check Digit Verification of cas no
The CAS Registry Mumber 63202-26-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,2,0 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 63202-26:
(7*6)+(6*3)+(5*2)+(4*0)+(3*2)+(2*2)+(1*6)=86
86 % 10 = 6
So 63202-26-6 is a valid CAS Registry Number.
63202-26-6Relevant academic research and scientific papers
Transglycosylation of β-D-ribofuranosylindazoles
Boryski
, p. 77 - 89 (2007/10/02)
Irreversible, acid-catalyzed 2 → 1 transglycosylation reactions of fully acetylated β-D-ribofuranosylindazoles were studied applying HPLC analysis. Results so obtained support the intermolecular mechanism of transglycosylation via a 1,2-diglycosylindazole intermediate and are compared to those of the purine series.
