6330-98-9 Usage
Uses
Used in Pharmaceutical Industry:
1-Methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is used as a building block or intermediate in the synthesis of various pharmaceutical products. Its unique structure and functional groups make it a valuable component in the development of new drugs and medicinal compounds.
Used in Agricultural Industry:
In the agricultural sector, 1-Methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is employed as a precursor in the production of agrochemicals. Its role in the synthesis of bioactive molecules contributes to the development of effective pesticides and other agricultural chemicals.
Used in Dyes and Pigments Industry:
1-Methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is used as a key component in the manufacture of dyes and pigments. Its chemical properties allow for the creation of a wide range of colors and hues, making it an essential ingredient in the production of various colorants.
Used in Biochemical Research:
1-Methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is utilized as a research compound in biochemical studies. Its potential biological activities, such as enzyme inhibition, make it a valuable tool for understanding biological processes and developing new therapeutic agents.
Used in Organic Synthesis:
As an organic compound, 1-Methyl-2-(methylsulfanyl)pyrimidin-4(1H)-one is used as a versatile intermediate in various organic synthesis processes. Its reactivity and functional groups enable the formation of a diverse array of chemical products, contributing to the advancement of organic chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 6330-98-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,3 and 0 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6330-98:
(6*6)+(5*3)+(4*3)+(3*0)+(2*9)+(1*8)=89
89 % 10 = 9
So 6330-98-9 is a valid CAS Registry Number.
6330-98-9Relevant academic research and scientific papers
The Tautomeric Equilibria of Thio Analogues of Nucleic Acid Bases. Part 1. 2-Thiouracil: Background, Preparation of Model Compounds, and Gas-phase Proton Affinities
Katritzky, Alan R.,Baykut, Gokhan,Rachwal, Stanislaw,Szafran, Miroslaw,Caster, Kenneth C.,Eyler, John
, p. 1499 - 1506 (2007/10/02)
The preparation is reported of all four the monoalkyl derivatives of 2-thiouracil and four of the six possible dialkyl derivatives required as models for a study of the tautomeric equilibria by physical methods.Gas-phase proton affinities are determined using ion cyclotron resonance mass spectrometry, and are used to provide quantitative estimates of individual tautomer stabilities in the vapour state.These quantitative results agree well with qualitative deductions of predominant structures for the monoalkyl derivatives from i.r. spectroscopy.
