89069-33-0 Usage
General Description
2-(methylsulfanyl)-3-[3-(trifluoromethyl)phenyl]pyrimidin-4(3H)-one is a chemical compound with the molecular formula C13H10F3N3OS. It is a pyrimidine derivative with a methylsulfanyl group at the 2-position and a trifluoromethylphenyl group at the 3-position. 2-(methylsulfanyl)-3-[3-(trifluoromethyl)phenyl]pyrimidin-4(3H)-one has potential applications in medical and pharmaceutical research due to its ability to interact with biological targets. It may also have uses in the field of agrochemicals or as a building block for the synthesis of other organic compounds. Its specific properties and potential uses would depend on further research and testing.
Check Digit Verification of cas no
The CAS Registry Mumber 89069-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,6 and 9 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 89069-33:
(7*8)+(6*9)+(5*0)+(4*6)+(3*9)+(2*3)+(1*3)=170
170 % 10 = 0
So 89069-33-0 is a valid CAS Registry Number.
89069-33-0Relevant academic research and scientific papers
Synthesis and Biological Activity of 2,6-disubstituted 3-Aryl-4(3H)-pyrimidones as Potential CNS Agents
Gupta, K. A.,Saxena, Anil K.,Jain, Padam C.,Dua, P. R.,Prasad, C. R.,Anand, Nitya
, p. 789 - 794 (2007/10/02)
The reaction of N-arylamidines (III) with appropriate 2-alkynoic ester gives 2,6-disubstituted 3-aryl-4(3H)-pyrimidones (IV) in one step except in the reaction of N-(2-trifluoromethylphenyl/biphenyl)-S-methylisothiourea with ethyl propiolate, where the required pyrimidones (IVa17/IVa20) along with the adduct (Va/Vb) have been isolated; these adducts on cyclisation yield the corresponding pyrimidinones (IVa17/IVa20). 2,3,6-Triphenyl-4(3H)-pyrimidone (IVh1) on treatment with P2S5 furnishes the corresponding thione (VI).Some of these compounds have shown significant central muscle relaxant, hypnotic, anticonvulsant, CNS depressant, antiinflammatory and diuretic activities.
