82859-59-4 Usage
Hydrazide derivative
pyrazolopyrimidine The compound is derived from pyrazolopyrimidine by the addition of a hydrazide group, which gives it unique properties and potential applications.
Potential antiviral agent
The compound has been studied for its potential as an antiviral agent, suggesting it may be effective in inhibiting the replication or spread of certain viruses.
Potential cancer treatment
Research has also explored the use of 1H-Pyrazolo[3,4-d]pyrimidine-3-carboximidic acid, 4-hydrazino-,
hydrazide as a potential treatment for certain types of cancers, indicating its potential as a targeted therapy or chemotherapeutic agent.
Versatile building block
The hydrazide group in the compound makes it a versatile building block for the synthesis of various biologically active compounds, allowing for the creation of new drugs and therapies.
Medicinal chemistry and drug discovery interest
The structure and properties of 1H-Pyrazolo[3,4-d]pyrimidine-3-carboximidic acid, 4-hydrazino-, hydrazide make it of interest to researchers in the field of medicinal chemistry and drug discovery, as it may lead to the development of new and effective treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 82859-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,8,5 and 9 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 82859-59:
(7*8)+(6*2)+(5*8)+(4*5)+(3*9)+(2*5)+(1*9)=174
174 % 10 = 4
So 82859-59-4 is a valid CAS Registry Number.
82859-59-4Relevant academic research and scientific papers
SYNTHESIS OF 3-SUBSTITUTED 4-METHYLMERCAPTO- AND 4-AMINOPYRAZOLOPYRIMIDINES AND THEIR RIBOSIDES
Bulychev, Yu. N.,Korbukh, I. A.,Preobrazhenskaya, M. N.
, p. 210 - 215 (2007/10/02)
3-Cyano-4-methylmercaptopyrazolopyrimidine, fusion of which with 1,2,3,5-tetra-O-acetyl-β-D-ribofuranose gave its per-O-acetylated 1-β-D-ribofuranoside in 61percent yield, was synthesized from 3,4-dicyano-5-aminopyrazole.O-Deacetylation of the per-O-acetylated 1-β-D-ribofuranoside was carried out by the action of 1percent HCl in methanol. New pyrazolopyrimidines were obtained by the reaction of 3-cyano-4-methylmercaptopyrazolopyrimidine and its 1-riboside, as well as 3-cyano-4-aminopyrazolopyrimidine, with a number of nucleophilic reagents.The cytotoxic activities of the compounds obtained were studied.
