3298-76-8 Usage
Uses
Used in Pharmaceutical Synthesis:
8-phenyl-3,7-dihydro-6H-purine-6-thione is used as a key intermediate in the synthesis of various pharmaceutical drugs, leveraging its unique chemical properties to facilitate the development of new therapeutic agents.
Used in Anticancer Applications:
In the field of oncology, 8-phenyl-3,7-dihydro-6H-purine-6-thione is used as a potential anti-cancer agent, targeting enzymes and proteins involved in cancer cell proliferation. Its ability to inhibit these targets makes it a promising candidate for the development of new cancer treatments.
Used in Antiviral Applications:
8-phenyl-3,7-dihydro-6H-purine-6-thione is also used as a potential antiviral agent, with research indicating its capacity to interfere with viral replication processes, offering a new avenue for the treatment of viral infections.
Used in Neuroprotection:
In the neuroscience field, 8-phenyl-3,7-dihydro-6H-purine-6-thione is used for its neuroprotective effects, which may contribute to the development of therapies for neurodegenerative diseases by protecting neurons from damage.
Used in Antioxidant Therapies:
8-phenyl-3,7-dihydro-6H-purine-6-thione is utilized for its antioxidant properties, which can be harnessed in the development of treatments aimed at combating oxidative stress-related conditions and promoting overall health.
Check Digit Verification of cas no
The CAS Registry Mumber 3298-76-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,9 and 8 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 3298-76:
(6*3)+(5*2)+(4*9)+(3*8)+(2*7)+(1*6)=108
108 % 10 = 8
So 3298-76-8 is a valid CAS Registry Number.
3298-76-8Relevant academic research and scientific papers
Tandel, Sagun,Bliznets, Igor,Ebinger, Katalin,Ma, You-An,Bhumralkar, Dilip,Thiruvazhi, Mohan
, p. 2321 - 2322 (2004)
A one-pot synthesis of 6-mercaptopurines from 4,5-diamino-6-chloro- pyrimidine, an aldehyde and elemental sulfur is presented. The key advantage of this procedure is that it utilizes the in situ generated H2S to convert the chloro to a mercapto group.
