6014-07-9 Usage
1-Phenyl-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidine-4-thione properties and specific content
A chemical compound consisting of 11 carbon atoms, 9 hydrogen atoms, 3 nitrogen atoms, and 1 sulfur atom.
Chemical structure
Pyrazolo[3,4-d]pyrimidine derivative
A heterocyclic compound with a pyrazole ring fused to a pyrimidine ring, featuring a sulfur atom and various substituents.
Phenyl group attachment
Nitrogen atom at position 1
A benzene ring connected to the nitrogen atom in the pyrazolo[3,4-d]pyrimidine core, which influences the compound's properties and activities.
Pharmaceutical and biological activities
Antifungal, antiproliferative, and antiviral properties
The compound exhibits potential therapeutic effects against fungal infections, cell proliferation, and viral infections.
Potential applications
Development of new drugs for various diseases
The compound may be useful in creating novel pharmaceuticals for treating a range of medical conditions.
Research status
Further research needed
Additional studies are required to fully understand the therapeutic potential and mechanism of action of 1-phenyl-1,2-dihydro-4H-pyrazolo[3,4-d]pyrimidine-4-thione.
Check Digit Verification of cas no
The CAS Registry Mumber 6014-07-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,1 and 4 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6014-07:
(6*6)+(5*0)+(4*1)+(3*4)+(2*0)+(1*7)=59
59 % 10 = 9
So 6014-07-9 is a valid CAS Registry Number.
6014-07-9Relevant academic research and scientific papers
Synthesis of some new biologically active sulfur compounds containing pyrazolo[3,4-d] pyrimidine moiety
Ismail, Zeinab H.,Abdel-Gawad, Soad M.,Abdel-Aziem, Anhar,Ghorab
, p. 1795 - 1805 (2007/10/03)
A novel series of the pyrazolo[3,4-d]pyrimidines having biologically active sulfur moieties 3-20 were prepared via reaction of 4-mercapto-1-phenyl-1H-pyrazolo[3,4-d]pyrimidine 3 with different reagents. Identification of the new compounds was established by elemental analyses, IR, 1H-NMR, and mass spectral data. Some of the obtained compounds showed the interesting antimicrobial activity comparable to antibiotic chloramphenicol as standard antibacterial agent and Terbinafin as a standard antifungal agent.
Electrophilic cyanations. I. Synthesis of thiocyanato-heteroarenes and tosylheteroarenes from mercapto-heteroarenes using p-toluenesulfonyl cyanide
Miyashita, Akira,Nagasaki, Izuru,Kawano, Akiko,Suzuki, Yumiko,Iwamoto, Ken-Ichi,Higashino, Takeo
, p. 745 - 755 (2007/10/03)
Mercaptoheteroarenes (1) underwent electrophilic cyanation with p-toluenesulfonyl cyanide (TsCN) in THF in the presence of NaH to give the corresponding thiocyanatoheteroarenes (2) in moderate to good yields. In DMF, tosylheteroarenes (4) were formed by substitution with p-toluenesulfinate ion through thiocyanatoheteroarenes (2).
