6327-98-6 Usage
Uses
Used in Pharmaceutical Synthesis:
2-(Methylthio)-3-methylpyrimidine-4(3H)-one is used as an intermediate in the synthesis of pharmaceuticals for its ability to contribute to the development of new drugs with potential therapeutic effects.
Used in Agrochemical Production:
In the agrochemical industry, 2-(Methylthio)-3-methylpyrimidine-4(3H)-one serves as an intermediate, aiding in the creation of compounds that can be used in various agricultural applications to protect crops and enhance yields.
Used in Medicinal Chemistry Research:
2-(Methylthio)-3-methylpyrimidine-4(3H)-one is utilized in research for its potential antimicrobial properties, making it a candidate for the development of new antibiotics to combat resistant bacteria.
Used in Drug Development for Antitumor Properties:
Owing to its potential antitumor properties, 2-(Methylthio)-3-methylpyrimidine-4(3H)-one is explored in drug development for its capacity to inhibit tumor growth, offering a new avenue for cancer treatment.
Check Digit Verification of cas no
The CAS Registry Mumber 6327-98-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,2 and 7 respectively; the second part has 2 digits, 9 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6327-98:
(6*6)+(5*3)+(4*2)+(3*7)+(2*9)+(1*8)=106
106 % 10 = 6
So 6327-98-6 is a valid CAS Registry Number.
InChI:InChI=1/C6H8N2OS/c1-8-5(9)3-4-7-6(8)10-2/h3-4H,1-2H3
6327-98-6Relevant academic research and scientific papers
Methyl orthocarboxylates as methylating agents of heterocycles
Janin, Yves L.,Huel, Christiane,Flad, Genevieve,Thirot, Sylvie
, p. 1763 - 1769 (2007/10/03)
Methylation reactions occurring between trimethyl orthocarboxylates or N,N-dimethylcarboxamide dimethyl acetals and various hydroxylated heterocycles, involving a lactam-lactim tautomeric equilibrium, were investigated as an alternative to classic methyla
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.
