6112-71-6 Usage
Uses
Used in Organic Synthesis:
[(6-Amino-1,4-dihydro-4-oxopyrimidin)-2-yl]cyanamide is used as a reagent for the synthesis of various organic compounds, playing a crucial role in the creation of new chemical entities.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, [(6-Amino-1,4-dihydro-4-oxopyrimidin)-2-yl]cyanamide is utilized for its potential biological activities, which include antibacterial and anti-tumor properties. This makes it a valuable compound in the development of new drugs and therapies.
Used in Cancer Treatment Research:
[(6-Amino-1,4-dihydro-4-oxopyrimidin)-2-yl]cyanamide is studied for its potential use in the treatment of cancer due to its anti-tumor properties, offering a promising avenue for research into novel cancer therapies.
Used in Tuberculosis Treatment Research:
Additionally, [(6-Amino-1,4-dihydro-4-oxopyrimidin)-2-yl]cyanamide has been investigated for its potential application in the treatment of tuberculosis, indicating its broad spectrum of potential therapeutic uses.
Check Digit Verification of cas no
The CAS Registry Mumber 6112-71-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,1,1 and 2 respectively; the second part has 2 digits, 7 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 6112-71:
(6*6)+(5*1)+(4*1)+(3*2)+(2*7)+(1*1)=66
66 % 10 = 6
So 6112-71-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H5N5O/c6-2-8-5-9-3(7)1-4(11)10-5/h1H,(H4,7,8,9,10,11)
6112-71-6Relevant academic research and scientific papers
Microwave-expedited one-pot, two-component, solvent-free synthesis of functionalized pyrimidines
Goswami, Shyamaprosad,Jana, Subrata,Dey, Swapan,Kumar Adak, Avijit
, p. 120 - 123 (2008/02/11)
The synthesis of a series of diversely substituted pyrimidines under solvent-free conditions in good yields is described. Under microwave irradiation, a variety of nucleophilic substrates containing the N?C?N unit with ?-dicarbonyl compounds, ethyl cyanoacetate, malononitrile, and chalcones was cyclized to give pyrimidines. A combinatorial type approach for a one-step synthesis has been developed where a ring-closing condensation is followed by spontaneous aromatization to afford 28 functionalized and aryl/alkyl substituted pyrimidines. CSIRO 2007.
